ISSN 0006-2979, Biochemistry (Moscow), 2025, Vol. 90, Suppl. 2, pp. S444-S475 © Pleiades Publishing, Ltd., 2025.
S444
REVIEW
The Discovery of Magnetic Resonance
in the Context of 20th Century Science:
Biographies and Bibliography.
III: First Decades in the Soviet Union Following
the Discovery of Magnetic Resonances in Matter
Alexander V. Kessenikh
1#
and Vasily V. Ptushenko
2,3,a
*
1
Vavilov Institute for the History of Science and Technology, Russian Academy of Sciences,
125315 Moscow, Russia
2
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University,
119992 Moscow, Russia
3
Emanuel Institute of Biochemical Physics, Russian Academy of Sciences,
119334 Moscow, Russia
a
e-mail: ptush@belozersky.msu.ru
Received December 25, 2025
Revised December 25, 2025
Accepted December 30, 2025
AbstractTo some extent, fortune favored announcement of the ERP discovery: Zavoisky’s paper was pub-
lished fairly promptly in both Russian and in English in 1945 and thus fortunately slipped through the
tiny gap between the two epochs – just in time before the Iron Curtain descended across Europe. Thus,
scientists beyond the borders of the USSR became aware of the discovery and were in fact the first to cite
and acknowledge Zavoisky’s work. In 1944-early 1945, Zavoisky delivered his paper at a series of seminars
attended by a number of renowned physicists, chemists, chemical physicists, biophysicists, and geophysicists
from the USSR’s best scientific institutions. Nevertheless, for nearly a decade EPR had been of interest al-
most exclusively to physicists who belonged to Zavoisky’s school he established in Kazan. Beyond Kazan,
A.  I.  Shalnikov, P.  L.  Kapitsa, and Ya.  K.  Syrkin appeared to have been the only scientists in the Soviet Union
who immediately recognized promise of the EPR discovery. Moreover, there were the works of Syrkin’s
student L.  A.  Blumenfeld and his friend V.  V.  Voevodsky that paved the way for the EPR method to spread
beyond Kazan and physics, into chemistry and biology research all across the USSR. After late 1950s, the
number of publications on EPR in Soviet journals grew exponentially. Research groups studying magnetic
resonance phenomena were established in many other scientific institutions. In the present paper, those
groups and their studies, as well as scientific instrumentation for EPR and NMR spectroscopy in the USSR
are briefly discussed.
DOI: 10.1134/S0006297925604502
Keywords: Ya. K. Syrkin, L. A. Blumenfeld, V. V. Voevodsky, chemical and biological radiofrequency spectroscopy,
acoustic resonance, spin relaxation, nuclear polarization, spin chemistry, scientific instrumentation
# Deceased.
* To whom correspondence should be addressed.
DISCOVERY AND ITS ANNOUNCEMENT
Irrespective of the magnitude, from the sci-
ence point of view a discovery is “born” on the day
when the findings are published. Fortune favored
announcement of the ERP discovery: the paper was
published fairly promptly in both Russian language
[1] and in English [2], which at that time started to
gain its status of international language of science.
Zavoisky’s findings fortunately slipped through the
tiny gap between the two epochs – “Iron curtain”
FIRST DECADES IN THE SOVIET UNION S445
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
was about to descend across Europe. In just two
years, the Journal of Physics, USSR, a Soviet English-
language peer-reviewed journal, where Zavoisky pub-
lished his first paper (followed later by a number of
his other works), would be shut down and Soviet
scientists would eventually be completely cut off
any opportunity to share their discoveries with their
peers on the other side of the Iron Curtain.
In terms of informing the international scientific
community of the EPR discovery, Zavoisky’s publica-
tion in the Journal of Physics, USSR, was definitely
instrumental. Earlier in this book, the role this pa-
per might have (or might have not) played in the
Purcell’s and in F.  Bloch’s discovery of the nuclear
magnetic resonance was already discussed. Although
it came out too late to have a strong direct influ-
ence on the work of any of the two, it had become
available for the Western scientists by the time both
Purcell and Bloch were already conducting their ex-
periments. Ironically, the very issue of the Physical
Review journal (issue  69, 1946) in which F.  Bloch
published his NMR research findings contained a
reference to the article from the very issue of the
Journal of Physics, USSR, in which E.  K.  Zavoisky pub-
lished his EPR research findings. As if this was not
a big enough coincidence, they were placed on the
same page! This circumstance, spotted by N.  E.  Za-
voiskaya [3], speaks to the fact that the Soviet En-
glish-language journal, meaning all the papers pub-
lished in it, was available to and scanned by scholars
in the West.
The press was not the only channel to make the
EPR discovery known to the scientific community. By
June  1944, Zavoisky finalized his doctoral dissertation
presenting his findings and submitted it to the Phys-
ical Institute of the USSR Academy of Sciences, Mos-
cow (now the Lebedev Physical Institute or LPI) [4].
On December  30, 1944, he delivered his paper at a
seminar at the Institute for Physical Problems (IPP)
now bearing the name of P.  L.  Kapitsa, the famous
“kapitsnik”
1
as called among Soviet physicists. Quite
a number of renowned Soviet physicists, chemists,
chemical physicists, biophysicists, and geophysicists
from the USSR’s best scientific institutions attend-
ed that seminar. Among the participants there were
academician A.  F.  Ioffe, “farther of the Soviet phys-
ics” and director of the Physical-Technical Institute
(now the Ioffe Institute); academician N.  N.  Semenov,
director of the Institute of Chemical Physics of the
USSR Academy of Sciences
2
, and a number of his
fellow scientists, including Ya.  B.  Zeldovich, I.  L.  Zel-
manov, and Yu.  N.  Ryabinin; G.  S.  Gorelik, a promi-
nent radio physicist, who at the time worked with
A.  A.  Andronov at the Gorky State University
3
, the
cradle of oscillation theory; G.  N.  Flerov, one of the
founders of the Soviet nuclear program (Laborato-
ry No.  2); E.  V.  Shpolsky (Moscow State Pedagogical
Institute
4
), co-founder and lifelong editor of the So-
viet Physics Uspekhi journal; K.  V.  Vladimirskii from
the Physical Institute, who, a year later, would au-
thor the first ever publication on NMR in the Soviet
Union; S.  E.  Bresler, a physicist, a chemical physicist,
and a biophysicist; many of the renowned scientists
from the IPP, including L.  D.  Landau, E.  M.  Lifshitz,
A.  B.  Migdal, Y.  A.  Smorodinsky, E.  L.  Andronikashvili,
and, of cause, A.  I.  Shalnikov, who helped Zavoisky to
reproduce his experiment in Moscow, and academi-
cian P.  L.  Kapitsa, the host of the event. The seminar
was also attended by the scientists from the Institute
of Geological Sciences
5
, Laboratory for Geochemical
Problems
6
, Moscow State University’s Research Insti-
tute of Physics, and from other schools [5]. That is to
say, Zavoisky shared his findings with a multidisci-
plinary audience representing the country’s major sci-
entific institutions. A month later, on January  30, 1945,
Evgeny Konstantinovich defended his dissertation at
the Physical Institute of the USSR Academy of Scienc-
es with the crème de la crème of the Soviet physics
sitting in the Dissertation Committee. Among his doc-
toral thesis opponents there were S.  I.  Vavilov (Pres-
ident of the Committee), G.  S.  Landsberg, S.  M.  Rytov,
V.  I.  Veksler, V.  L.  Levshin, E.  I.  Kondorsky, and, again,
A.  I.  Shalnikov [6]. The list of attendees is obviously
far from complete, for both events. In other words,
quite a representative part of the Soviet scientif-
ic community, hardly confined to physicists only,
was given a firsthand account of the EPR exper-
iment.
For some unknown reason, the discovery made
by E.  K.  Zavoisky escaped attention of the Soviet
science. Analysis of the Soviet scientific literature
shows that it had little to no presence on the pag-
es of the peer-reviewed journals of that time. Ap-
parently, neither was his or his collaborators’ work
1
A wordplay about the surname Kapitsa.
2
Now N. N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences.
3
Now Lobachevsky State University of Nizhny Novgorod.
4
Now Moscow State Pedagogical University.
5
Now Geological Institute of Russian Academy of Sciences.
6
Now Vernadsky Institute of Geochemistry and Analytical Chemistry of Russian Academy of Sciences.
KESSENIKH, PTUSHENKOS446
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
on EPR, a topic commonly discussed at the scientific
gatherings held in the Soviet Union in that period.
The biggest and most relevant (in the context of EPR)
conferences took place in December 1946– two years
after Zavoisky had first announced his findings at the
IPP seminar and a year and a half after his ground-
breaking paper had been published. They were: the
Meeting on Electric Oscillations and Electric Waves
in Gorky
7
(9-12 December, 1946), organized by the
All-Union Scientific Council for Radiophysics and Ra-
dio Technology (the USSR Academy of Sciences) and
by the Gorky State University [7]; the 5th All-Union
Conference on Spectroscopy held in Leningrad
8
(10-16 December, 1946) organized by the Commission
for Spectroscopy (Academy of Sciences, USSR) [8];
the First All-Union Conference on Physics of Magnet-
ic Phenomena in Sverdlovsk
9
(11-16 December, 1946)
organized by the USSR Academy of Sciences (Depart-
ment of Physical and Mathematical Sciences) and its
Ural Branch [9]. The latter was the most relevant in
the context of magnetic resonance, its program cov-
ering topics like “Nuclear Magnetic Moments in Solids
and in Liquids” and “Nuclear Magnetism”. According
to the report published by the Bulletin of the USSR
Academy of Sciences, “apart from Sverdlovsk physi-
cists, the Conference was attended by magnetologists
from Moscow, Leningrad, Kharkov, Kazan, Gorky,
Chelyabinsk, Molotov
10
, and Krasnoyarsk. A total of
9 plenary sessions were held with over 40 papers
delivered” (Vonsovsky, 1947). The list of speakers in-
cluded prominent Soviet physicists like V.  K.  Arkad-
yev, Ya.  I.  Frenkel, Ya.  G.  Dorfman, E.  I.  Kondorsky,
L.  V.  Kirensky, and S.  V.  Vonsovsky. According to
N.  E.  Zavoiskaya, B.  M.  Kozyrev, Zavoisky’s collabo-
rator, was among the attendees as well [3]. Evgeny
Konstantinovich was also invited [4], although he was
not among the speakers.
De facto the only paper to some extent pertaining
to magnetic resonance was delivered by Ya.  G.  Dorf-
man (“Nuclear magnetic moments in the condensed
phase”) [10]. He was the only speaker at the Confer-
ence who referred to Zavoisky’s experiment (he at
least did mention his work!). This reference, though,
was in the context of magnetic resonance methods
being “equivalent to magnetomechanical methods”
and “hardly useful for determining nuclear magnet-
ic moments in the condensed systems”. Judging from
the Conference materials that were published  [9],
no other speaker mentioned the discovery of EPR.
N.  E.  Zavoiskaya wrote about this in her book: “Cu-
riously, none of the speakers at the Conference said
a word on the promise of Zavoisky’s pioneering re-
search. Neither Ya.  I.  Frenkel, nor V.  K.  Arkadyev, nor
Ya.  G.  Dorfman considered his discovery to be out-
standing, that is to say promising, the first two know-
ing Zavoisky personally and being acquainted with
his work firsthand” [3]. Time brought about a little
change. A year later, on September28, 1947, A.  F.  Ioffe,
farther of the Soviet physics, delivered a commemo-
rative speech “Thirty Years of the Soviet physics” (to
celebrate the 30th anniversary of the October Rev-
olution of 1917). Quite a number of lines of inves-
tigation and fields of study that had emerged since
1917 received an honorable mention from him. EPR,
though, was not among the advancements he consid-
ered worth noting [11]. In the same 1947, I.  K.  Kikoin,
when reviewing Zavoisky’s paper nominated for the
Stalin Prize
11
, all but doubted the existence of EPR as
a phenomenon: “If this hypothesis proves valid, phys-
icists would obtain a simple and powerful method for
determining nuclear magnetic moments…” [3].
Given a plethora of magnetic resonance studies
and research burgeoning in the West, both in Europe
and in the United States (a fact the Soviet physics
could not have been totally ignorant about), such
an attitude seems strikingly peculiar. Noteworthily,
in1947 (in January, 1948, at the latest), C.  Gorter and
G.  Wentzel nominated F.  Bloch for the Noble Prize in
Physics. Magnetic resonance research was growing
dramatically. Within several years that passed since
F.  Bloch and E.  M.  Purcell had each published his find-
ings, hundreds of papers pertaining to magnetic reso-
nance (EPR, NMR, nuclear quadrupole resonance and
ferromagnetic resonance included) were published.
New resonance-related phenomena and instrumenta-
tion was frequently the talk of major international
scientific gatherings. In 1948-1949, a rare meeting of
the American Physical Society (APS) failed to discuss
related problems. In 1949, for example, as many as
25 papers on the new phenomenon were delivered
(for a selected list of papers see Online Resource  1).
In 1948, APS held a Symposium on Microwave and
Radio-Frequency Spectroscopy with another gath-
ering, a Radio-Frequency Spectroscopy Conference,
taking place at Oxford University in the same year,
and yet another one held in 1950 in Amsterdam.
7
Now Nizhny Novgorod.
8
Now St. Petersburg.
9
Now Ekaterinburg.
10
Now Perm.
11
The highest honor in the Soviet Union bestowed in recognition of a single piece of work in science or culture.
The Prize was established in 1939 and existed till 1955. Later it was given the same status as the newly established
(in 1966) State Prize of the USSR.
FIRST DECADES IN THE SOVIET UNION S447
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 1. Ya.  K.  Syrkin (left), his former student and long-time co-author M.  E.  Dyatkina (right) and their colleagues in the
Kurnakov Institute of General and Inorganic Chemistry, 1960s. Source: personal archive of S.  P.  Dolin.
Each attracted researchers from all over the world:
the Unites States, the United Kingdom, the Nether-
lands, Japan, France, Sweden, Switzerland, and Ger-
many [3]. At the Oxford Conference in 1948, C.  Gorter
acknowledged E.  K.  Zavoisky’s priority of discovery.
Paradoxically, Western scientists paid much more
attention to Zavoisky’s findings and had been refer-
ring to his works before his fellow Soviet physicists
did. Cummerow and Halliday [12] were the first to
refer to Zavoisky and his discovery [2] in their paper.
C.  Gorter was next with his book [13]. Meanwhile in
the USSR, apart from Ya.  G.  Dorfman who referred to
Zavoisky’s findings at the Conference in Sverdlovsk
(as mentioned earlier), his work was for the first
time cited by V.  L.  Ginzburg in the Physics Uspekhi
(Advances in Physical Sciences) [14] along with the
papers by Purcell [15] and Bloch [16].
Basically, for nearly a decade EPR had been of
interest to physicists in Kazan almost exclusively. In
those years, any EPR-related developments in the
USSR were almost exclusively due to the efforts of
S.  A.  Altshuler (1911-1983) and B.  M.  Kozyrev (1905-
1979), Zavoisky’s friends and colleagues. Within ten
years after 1947 (the year when E.  K.  Zavoisky left
Kazan for Arzamas-16), the two of them published
over 70 research papers on various aspects of mag-
netic resonance (it was the overwhelming majority of
all the research published on the subject in the USSR
in that period). Those works are discussed in detail by
L.  K.  Aminov [17], Yu.  V.  Yablokov [18], N.  S.  Altshuler
and A.  L.  Larionov [19], and in the book “Paramag-
netic Resonance” [20].
Other research groups in this new area of scien-
tific inquiry emerged in the USSR later. Of them, the
first to be noted is the group led by A.  M.  Prokhorov,
the future Nobel Prize laureate. His group embarked
on its EPR-related investigations at the Physical In-
stitute in 1953, the first publications dated 1955
[21, 22]. A.  M.  Prokhorov obviously pursued his own
original ideas, yet his works on EPR were close-
ly related to the research performed by the Kazan
group of physicists – his EPR experimental work
started only after A.  A.  Manenkov, a post-graduate
student of B.  M.  Kozyrev, had come to work at the
Physical Institute. From then on, Manenkov played
a crucial part in the Prokhorov’s EPR experimenta-
tion. It must be acknowledged though, that the first
experiments performed by Manenkov and Prokhor-
ov were strongly influenced by the works published
by Bleaney and his group, the first to focus on
monocrystalline oxides and transition-element-doped
diamagnetic salts.
P.  L.  Kapitsa and A.  I.  Shalnikov appear to have
been the only physicists in the Soviet Union who
immediately recognized promise of the discovery
made by E.  K.  Zavoisky and his colleagues. They
both generously provided him with support, finan-
cial and administrative. For instance, he was offered
to reproduce his experiment at the IPP; its techni-
cal capabilities being much stronger than those of
the Kazan University. It was the Institute for Physi-
cal Problems that nominated Zavoisky for the Stalin
Prize. What is more, Kapitsa included EPR research
in the IPP’s scope of work for the year 1946 [23].
KESSENIKH, PTUSHENKOS448
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 2. Left to right: V.  V.  Voevodsky, L.  A.  Blumenfeld. Akademgorodok (science city), Novosibirsk, 1961. Source: M.  V.  Vo-
evodskaya’s personal archive.
Today, one can only speculate what could have been
the course of EPR research in the Soviet Union, had
Kapitsa not fallen from the grace in 1946, removed
from all of his positions and basically from science.
Thus, frustratingly, this line of EPR spectroscopy de-
velopment in the USSR was interrupted.
Apart from P.  L.  Kapitsa and A.  I.  Shalnikov, in
the Soviet scientific community only Ya.  K.  Syrkin, a
chemical physicist, was known to have a strong in-
terest in the EPR phenomena. Yakov Kivovich Syrkin
(1894-1974) (Fig.  1), an expert in theoretical chemis-
try well versed in quantum methods, chemical bonds
and molecular interactions, endeavored, in 1948, to
launch his own EPR-spectroscopy related research
[24] at Karpov Institute of Physical Chemistry, where
he was in charge of the Laboratory of Electric Prop-
erties of Molecules.
Since 1920, the focus of his attention had been
the development of physical methods for chemical
research (for example, [25]), including X-ray struc-
tural analysis, infrared vibrational spectroscopy, opti-
cal and electron methods (Kerr effect, depolarization,
anisotropic polarizability). He appears to have been
among the first in the USSR to use Raman scattering
in his chemical experimentation (for example, [26]).
In 1930s, he organized experimental studies of the
structure of chemical compounds with the use of the
dipole moments method (for example, [27]), the first
of its kind in the USSR. Finally, in mid-1940s his fo-
cus was on studying the chemistry of radicals, along
with editing the Russian translation of “The Chemis-
try of Free Radicals” by W.  A.  Waters [28]. Evidently,
it was due to his unique scientific background that
he could see right away potential of the EPR method
for chemical research. Syrkin entrusted the study of
the new method to L.  A.  Blumenfeld, his post-gradu-
ate student [24]. Yet, once again, ideological battles
inscience (the struggle against “the idealism in chem-
istry
12
”) and politics (“The Doctors Plot
13
”) put the
efforts of the two chemists on hold for several years.
Blumenfeld, however, managed to resume his sci-
entific investigations, when he got a job at the Cen-
tral Institute for Advanced Medical Education, Mos-
cow. There, his studies of oxygenation of hemoglobin
prompted him to revisit the idea of using EPR meth-
ods for his research. Change of magnetic properties
of proteins with oxygenation paved the way for EPR
spectroscopy to be Blumenfeld’s method of choice, af-
ter he had exhausted other methods (primarily, that
of magnetic balance). In the same period but in a
12
A campaign rejecting Pauling’s theory of resonance as antimaterialistic and anti-Marxist. The campaign was
prompted by the publication, in 1947, of the Russian translation of Pauling’s Nature of the Chemical Bond which
was done by Ya.  K. Syrkin and M.  E.  Diatkina. Both eventually had to leave the Karpov Institute of Physical Chem-
istry and lost almost all of their scientific posts. Only after 1957 Syrkin and Diatkina were able to resume their
structural chemistry related research.
13
An alleged conspiracy of prominent Soviet medical specialists to murder leading government and party of-
ficials (1953).
FIRST DECADES IN THE SOVIET UNION S449
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
different branch of chemistry (namely, free-radical
chemistry), another young chemist and Blumenfeld’s
friend, V.  V.  Voevodsky (Fig.  2), found himself in a
similar situation. Apparently, close scientific coop-
eration between the two young and enthusiastic re-
searchers and friends led to the “EPR virus” quickly
penetrating chemical kinetics and to the ERP spec-
troscopy finding its way into chemistry and biology
research. Ultimately, two new scientific schools or,
broadly speaking, two new fields of the Soviet science
were born: radio-frequency spectroscopy in chemistry
and radio-frequency spectroscopy in biology.
The first publications by L.  A.  Blumenfeld and
his collaborators [29, 30] pertained to the hypothesis
of A.  Szent-Györgyi (1941) for semiconductive prop-
erties of proteins, severely criticized by Soviet scien-
tists at the time (for example, [31]). In those early
papers, bio-tissues, proteins and isolated biochemical
substances exposed to ionizing radiation were stud-
ied. V.  V.  Voevodsky and his group, at the Institute of
Chemical Physics, started with investigating free rad-
icals produced by ionizing radiation as well [32,  33],
along with organometallic compounds [34], and gas-
phase chain chemical reactions [35].
From 1957 on, the number of papers on EPR spec-
troscopy and its numerous applications was growing
exponentially. In 1958-1960, V.  V.  Voevodsky and his
colleagues at the Institute for Chemical Physics alone
published over 30 research papers on EPR spectros-
copy’s potential for chemistry research. In the same
period, EPR methods began to increasingly “spread
out” across other scientific institutions and groups.
NUCLEAR MAGNETIC RESONANCE
NMR investigations, on the other hand, had an
earlier start in the USSR. K.  V.  Vladimirskii [36] led
the way in experimental research at the Physical In-
stitute in Moscow, and G.  R.  Khutsishvili  [37] of the
Institute of Physics in Tbilisi
14
pioneered in theoret-
ical studies of the phenomenon in the Soviet Union.
Noteworthily, G.  R.  Khutsishvili was an intern of
L.  D.  Landau, while K.  V.  Vladimirskii was Landau’s
doctoral student. L.  D.  Landau himself worked with
P.  L.  Kapitsa at the IPP and was among the first sci-
entists in the USSR to know about the discovery of
EPR. Late in the 1940s, at the Moscow State Univer-
sity, groups led by S.  D.  Gvozdover [38] and E.  I.  Kon-
dorsky  [39] launched their experimental research
programs on NMR as well. For the Soviet nuclear
program, NMR in matter was first observed in 1951
by G.  A.  Goncharov at the Thermal Technological Lab-
oratory of the USSR Academy of Sciences
15
. Later on,
though, similar research, including studies on NRM
in molecular beams, “moved” to Sukhumi Physi-
cal Technical Institute
16
. There, in Sukhumi, in July
1952, the first ever meeting on radio spectroscopy
in the Soviet Union took place. Papers on NMR were
delivered by speakers from the Physical Institute
(K.  V.  Vladimirskii) and from the Sukhumi Physical
Technical Institute (N.  I.  Leontyev) [40]. In Sukhumi,
some of the experiments on NMR were conducted by
W.  Hartmann, a German physicist. In that period, the
capabilities of instrumentation available to the Sovi-
et NMR researchers provided for quite modest out-
comes, a circumstance discussed in more detail later
in this Chapter.
Further development of NMR methods in the
USSR was delayed for decades, although rare efforts
to advance in this area that took place against all
odds, to some extent, set the stage for their future
evolution. S.  D.  Gvozdover and his laboratory at
the MSU
17
Department of Physics (N.  M.  Ievskaya,
N.  M.  Pomerantsev, and later – Yu.  S.  Kostantinov),
for example, persisted with their NMR experimen-
tation, although all they had at their disposal was
basically homemade apparatus. In 1951-1959, every
year one or two students graduated from the Mos-
cow State University with a specialization in NMR.
Up till 1957, NMR experiments could have only been
conducted with the use of rather primitive instru-
ments, like electromagnets capable of producing rath-
er inhomogeneous fields or like marginal oscillators
similar to those built by Pound and Hopkins. In those
years, NMR experiments were undertaken predomi-
nantly for demonstration purposes: to validate the-
oretically predicted resonance line shapes, to deter-
mine relaxation times by the logarithmic decrement,
to measure or stabilize magnetic field. In 1953-1961,
E.  I.  Kondorsky, at his laboratory at the MSU Depart-
ment of Physics, endeavored to study conduction-elec-
tron magnetization density with the use of the nu-
clear Overhauser effect, but to no avail, as some of
the physical laws involved were yet to be discovered
(namely, the mechanisms of nuclear and electron spin
relaxation in metals heavier than
7
Li, metal in which
the Overhauser effect was first observed). Needless to
say, those experiments at their core were reminiscent
of the works published abroad, mainly in the US.
14
Now the Andronikashvili Institute of Physics, Georgia.
15
Now the A.  I.  Alikhanov Institute of Theoretical and Experimental Physics.
16
Now the Ilia Vekua Sukhumi Institute of Physics and Technology, Georgia.
17
Lomonosov Moscow State University.
KESSENIKH, PTUSHENKOS450
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 3. NMR spectrometer built by L. L.  Dekabrun’s laboratory. Source: personal archive of E.  O. Vetrova.
Stronger effort to advance high resolution NMR
methods was undertaken by the Soviet scientists in
late 1950s-early1960s and was still drawing on the
international experience. At the MSU Department
of Physics, this effort was led by Y.  S.  Konstantinov
and N.  M.  Ievskaya. At the Physical Institute, a rel-
atively high-resolution spectrometer was developed
by K.  V.  Vladimirskii. Later, spectrometers using a
permanent magnet were designed in Moscow by
L.  L.  Dekabrun, V.  F.  Bystrov, and A.  U.  Stepanyants
of the Institute of Chemical Physics (Fig.  3), and in
Kazan by Y.  Y.  Samitov, A.  V.  Aganov et al. of the Ka-
zan State University. The latter two instruments were
ready for mass production but in the end only a cou-
ple of experimental models were assembled by the
Research & Development group (OKB in Russian) in
1963. All the designs referred to above provided for
resolution of the order of magnitude of 10
−7
,
while to
observe the proton magnetic resonance (PMR) a reso-
lution of 10
−8
to 10
−9
was required. In terms of reso-
lution and sensitivity, the early designs met the needs
of high-resolution
19
F and
31
P NMR research and were
put to use accordingly by Konstantinov (the Moscow
State University) assisted by the INEOS
18
chemists,
and by Y.  Y.  Samitov (the Kazan State University)
and B.  A.  Arbuzov (the Kazan Institute of Organic
Chemistry
19
), respectively. To some extent, those ear-
ly spectrometers were suitable for PMR studies of
organic acids and aldehydes, as well as of aromatic
compounds with aliphatic substituents (the difference
between proton chemical shifts exceeding 10
−6
), and
were indeed used in their research by V.  F.  Bystrov
and his colleagues from L.  L.  Dekabrun’s laboratory
at the Institute of Chemical Physics. In Leningrad
20
,
F.  I.  Skripov and his laboratory entered the field with
broad-line NMR studies (resolution of 10
−5
). In the
same period, Skripov’s laboratory, as well as their
colleagues in Sverdlovsk
21
, embarked on the develop-
ing the Earths’s field NMR technique. In Krasnoyarsk,
the A.  G.  Lundin’s research laboratory was making its
way into NMR spectroscopy with low-resolution NMR
studies as well. Meanwhile, according to A.  V.  Aganov,
the first task for the Samitov’s graduate students spe-
cializing in NMR was to demonstrate the Pake dou-
blet, or splitting of the resonance line shape in crys-
talline hydrates – a task requiring resolution of 10
−5
.
That is to say, international advances in the field set
the benchmark for the Soviet researchers irrespective
of the capabilities of the instrumentation available!
After the broad-line NMR, both in Kazan and in
Leningrad, studies continued into the high-resolution
19
F NMR spectra (the first dissertation on the subject
defended by P.  M.  Borodin at the Leningrad State Uni-
versity
22
, in 1955).
18
The Institute of Organoelement Compounds of the USSR Academy of Sciences.
19
Now the Arbuzov Institute of Organic and Physical Chemistry of the Russian Academy of Science.
20
Now St. Petersburg.
21
Now Ekaterinburg.
22
Now St. Petersburg State University.
FIRST DECADES IN THE SOVIET UNION S451
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
It was only in the late of 1950s that three re-
search groups were established in the USSR equipped
to develop modern (as of that time) high-resolution
NMR spectroscopy instrumentation for chemical in-
vestigations.
FERROMAGNETIC RESONANCE (FMR),
ACOUSTIC PARAMAGNETIC RESONANCE (APR),
AND ACOUSTIC NUCLEAR MAGNTIC
RESONANCE (ACOUSTIC NMR)
In the USSR, ferromagnetic resonance stud-
ies were mainly the domain of S.  V.  Vonsovsky [41]
at the Ural State University in Sverdlovsk. Early in
1950s, in the Soviet Union, the ferrites were in wide
use and thus were extensively studied and researched,
including with the use of resonance methods. At the
Ural University, such investigations were carried out
by S. V.  Vonsovsky, and at the Moscow University
by E. I. Kondorsky. In 1952, an excellent volume of
collected works on ferromagnetic, ferrimagnetic and
antiferromangetic resonances translated into Russian
was published, under the editorship of Vonsovsky. The
volume is cited in ChapterIV. Acoustic resonances the-
oretically predicted by S. A. Altshuler in 1952 were
experimentally studied in the early 1960s in Kazan,
in Kharkov (APR), and in Leningrad (acoustic NMR).
Some of the research is cited later, in the “geograph-
ical” review.
Following Kastlers metaphor [42] comparing EPR
and the Volga River beginning from a small spring
to become a mighty river, one must admit that, in
the USSR, ERP and magnetic resonance research in
general continued to be a small spring in those years.
As was said earlier, the amount of research papers on
the applications of EPR (and later NMR) spectroscopy
began to grow exponentially in the late 1950s prompt-
ing emergence of a number of new research groups,
institutes, and centers. Below is an overview of ma-
jor scientific schools and lines of research pertaining
to EPR and NMR spectroscopy, however incomplete
it might be. The time period discussed below for the
most part ends in 1969 – the 25th anniversary of the
EPR discovery. Let us start with Kazan– the birth city
of electron paramagnetic resonance, central for EPR
spectroscopy advancement in the Soviet Union.
MAJOR CENTERS FOR MAGNETIC RESONANCE
SPECTROSCOPY DEVELOPMENT IN THE USSR
Kazan: major lines of MR spectroscopy re-
search in 1950s-1960s. In Kazan, the first studies
of magnetic resonance phenomena were launched
by the Zavoisky’s EPR immediate collaborators
in two scientific institutions; S.  A.  Altshuler and
B.  M.  Kozyrev had close ties with, namely, the Kazan
State University and the Physical-Technical Institute
of the Kazan Branch of the USSR Academy of Sci-
ences. With time, their scientific schools developed
to intertwine with other Soviet research schools
and to entrain other Kazan-based institutions, such
as the Kazan Aviation Institute (KAI
23
), the Kazan
Branch of the Moscow Aviation Institute, the Kazan
Branch of the Moscow Power Engineering Institute,
the Institute of Organic and Physical Chemistry of
the Kazan Branch of the USSR Academy of Scienc-
es, Alexander Butlerov Institute of Chemistry, etc.
The scope of research was growing too as new dis-
coveries opened up new avenues for scientific inves-
tigation.
In 1952, S.  A.  Altshuler predicted resonant ab-
sorption of sound in paramagnetic media – the acous-
tic paramagnetic resonance (APR) [43]. From then on,
for many years, this phenomenon had been studied in
Kazan, both theoretically [44, 45] and experimentally
[46, 47]. Likewise, role of spin–phonon interactions
with regards to other phenomena (e.g., in antiferro-
magnets) was demonstrated by the S.  A.  Altshulers
students [48].
Findings by B.  I.  Kochelaev and L.  K.  Aminov,
of the Altshulers school, contributed to the “classic”
field as well – namely, to the theory of magnetic re-
laxation with regards to spin–lattice and spin–spin
interactions [49-51]. The new mechanism of paramag-
netic relaxation proposed by L.  K.  Aminov following
his studies of the two-step relaxation processes is
now known as the Orbach–Aminov processes.
EPR studies of the transition-metal complex ions
in isotropic solvents [52] set the stage for investiga-
tions of the said complex compounds in anisotropic
liquid crystalline solvents [53]. As a result, a whole
new field of research was born – magnetic liquid
crystals formed by coordination compounds [54-56].
Exchange interactions in the spin clusters were also
researched [57-59].
Of particular note are the investigations of EPR
in metals and in superconductors. To study metals,
magnetic resonance techniques were first used in
the 1950s-1960s by the founders of the Kazan EPR
school and their immediate students. One of the
first works on the subject [60] reported observation
of EPR in alkali metals (Li and Na) and dependence
of the resonance line shape on the size of metal-
lic particles. Akin to other ERP researchers of his
time, N.  S.  Garifyanov used a homemade spectrom-
eter in his experiments. The line shape asymmetry
23
Now the Kazan National Research Technical University named after A. N.  Tupolev – KAI.
KESSENIKH, PTUSHENKOS452
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
he observed was in qualitative agreement with the
Dyson’s theoretical description [61]. Later, after the
Laboratory of Metal Physics (E.  G.  Kharakhashyan,
laboratory chief) was set up at the Physical-Technical
Institute in 1974, the problem of the EPR line shape
for conduction electrons was thoroughly studied by
I.  G.  Zamaleev in thin films [62], and by Y.  I.  Talanov
in spherical particles [63].
Apart from the line shape, no less important is
the problem of spin relaxation of conduction elec-
trons, its mechanisms and relaxation channels, was
investigated at the Laboratory. In particular, the scope
of studies covered the impurity-dependent relaxation
(due to spin–orbit interaction) [64], relaxation at a
metal surface [65], and relaxation in metallic lithium
(due to the spin-current mechanism) [66]. It should
be noted that the latter research employed the tech-
nique of EPR relaxometry and reported a record nar-
row EPR line observed in the samples of LiF single
crystals – 0.04G  (!) – at room temperature, with the
use of the conduction–electron spin–echo method
[67]. Apart stood the studies of electron spin–lattice
relaxation in the metallic nanoparticles in which, by
means of the electron–spin–echo method, freezing of
spin–lattice relaxation of conduction electrons (due
to the energy levels indicative of the quantum size
effect) was directly observed (in alkali metal parti-
cles: silver and magnesium) [68,69]. In the West, this
experiment was reproduced only over a decade lat-
er [70].
To observe EPR in superconductors, the problem
of magnetism and superconductivity being incompati-
ble must have been solved. Magnetic field needed for
the EPR to be observed destroys superconductivity in
the type-I superconductors and makes the type-II su-
perconductors transit to the mixed (vortex) state (if
H
c1
 <H <H
c2
). That is to say, superconducting ma-
terials with λ magnetic field penetration depth and
a critical field H
c2
stronger than the resonance field
must have been found. Once they were determined
(La
3-x
GdxIn and La
1-x
Er
x
), S.  A.  Altshuler and his col-
leagues at the Physical-Technical Institute in Kazan
were the first in the world to observe EPR in super-
conductors [71, 72]. A year later, in the US, a similar
paper by R.  Orbach [73], who was studying the same
phenomenon, was published. (With regard to priority
of the discovery, it must be said that in the US it took
less time for the findings to be published in compar-
ison with the USSR.)
After high-temperature superconductivity was
discovered in 1987, EPR studies of the electronic
phase separation [74] and the resulting local magnet-
ic field distribution [75] were conducted, along with
the studies of the properties of the high-temperature
superconductivity energy spectrum; of vortex lattice;
of spin waves in superconductors [76]; etc. To per-
form some of the experiments, the EPR slide screw
tuner (~0.1  mm in size) scheme had to be devel-
oped [77].
After, in 1947, B.  M.  Kozyrev and S.  G.  Salikhov
published their paper on paramagnetic relaxation in
pentaphenylcyclopentadiene [78], the first work on
EPR spectroscopy in chemistry in the USSR, it was not
until the late 1950s that this line of research began
to develop. In 1960s, starting with [79], EPR spectros-
copy for chemical research was mostly the domain of
N.  S.  Garifyanov, Y.  V.  Yablokov, and some of their col-
leagues [80, 81]. In particular, intra- and intermolec-
ular interactions and corresponding relaxation times
were investigated in cooperation with A.  E.  Arbuzov
and F. G.  Valitova, the latter assisting with the chem-
ical side of the experiments. In 1958, A.  V.  Ilyasov, a
chemical physicist, developed an interest in this new,
unexplored avenue of research as well; G.  S.  Vozd-
vizhensky, N.  V.  Gudin and M.  S.  Shapnik, all of the
three electrochemists, joined him shortly. It was due
to their efforts that EPR studies of electrode processes
were launched [82,83]. In the late 1960s, A.  V.  Ilyasov,
Y.  M.  Kargin, and Y.  A.  Levin embarked on the devel-
opment of the method of electrochemical generation
of free radicals [84] (Fig. 4).
Since 1950s, NMR spectroscopy had also been
used in experiments in chemistry (by Y.  Y.  Samitov,
at first at the Kazan State University, and later – at
the Institute of Organic and Physical Chemistry of the
Kazan Branch of the USSR Academy of Sciences).
In conclusion, it must be said that in Kazan, in
addition to the wide range of original research being
carried out, the All-Union Conference on Magnetic
Resonance took place on a regular basis (every two
years starting with 1955), its themes and speakers’
geographical origins becoming ever more diverse
with time (Fig. 5).
Moscow: some of the EPR and NMR spectrosco-
py developments in the 1950s-1970s. Beyond Kazan,
among the first who relied on EPR spectroscopy
was A.  M.  Prokhorov’s group in Moscow. After its
first research was published in 1955 [21], the group
proceeded to a broad-scale investigation (or “scan-
ning”, in modern language) of paramagnetic crystals
[85-87] in search of the materials for quantum elec-
tronics [88]. The Physical Institute of the Academy of
Sciences continued to be the “headquarters” of EPR
studies in Moscow. In 1954 it was joined by the Re-
search Institute of Nuclear Physics
24
, Moscow State
University, after A.  M.  Prokhorov had been appoint-
ed the head of the Laboratory of Radio Spectrosco-
py there. The newly established Institute of Radio
24
Now Skobeltsyn Institute of Nuclear Physics (SINP MSU).
FIRST DECADES IN THE SOVIET UNION S453
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig.  4. V.  N.  Linev (left), I. V.  Ovchinnikov (center), J.  Hyde, (3rd right), A.  V.  Ilyasov (2nd right), Y.  V.  Yablokov (right) at
the XXIV Congress Ampere on Magnetic Resonance and Related Phenomena, Poznan, 1988. Source: personal archive of
V.  N. Linev.
Fig.  5. Left to right: ?, H. C.  Pfeiffer, H.  Benoît, ?, C.  Franconi, A. Lösche, E.  K.  Zavoisky, B.  M. Kozyrev, N.  S. Garifyanov at
the Conference on Magnetic Resonance in Kazan, 1969. Source: personal archive of Y.  I. Talanov, the author M.  L.  Blatt.
Engineering and Electronics of the Soviet Academy
of Sciences
25
became another center for magnetic
resonance research after M.  E.  Zhabotinsky, a col-
league of A.  M.  Prokhorov moved there from the
Physical Institute. The Institute of Radio Engineering
and Electronics eventually attracted a strong group
of experimental and theoretical physicists (M.  I.  Ro-
dak, A.  E.  Mefed, V.  A.  Atsarkin etal.), who performed
classic studies of magnetic relaxation and spin–
spin interactions, and verified experimentally the
B.  N.  Provotorov’s theory of cross relaxation (and the
two adjacent energy reservoirs created as a result)
[89-91].
Along with physical phenomena, EPR and NMR
spectroscopy was gaining momentum as a meth-
od for chemical and biological research. The works
25
Now Kotelnikov Institute of Radio Engineering and Electronics (IRE) of the Russian Academy of Sciences.
KESSENIKH, PTUSHENKOS454
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 6. Left to right: G.  I. Likhtenshtein, A.  L.  Buchachenko, E.  G.  Rozantsev, and N.  N.  Semenov, 1977. Source: [232], courtesy
to G.  I. Likhtenshtein.
Fig.  7. L. L.  Dekabrun (left) and O. D.  Vetrov (center). Source: personal archive of E.  O. Vetrova.
discussed below are classified as EPR in chemistry or
EPR in biology only arbitrary, for obvious reasons.
NMR spectroscopy in chemistry. At the Institute
of Physical Chemistry, magnetic resonance studies
were launched in the late 1950s by M.  B.  Neiman’s
group – A.  L.  Buchachenko, G.  I.  Likhtenshtein, and
E.  G.  Rozantsev, his students and colleagues. Out of
their research spin chemistry was eventually born
(A.  L.  Buchachenko, Y.  N.  Molin, K.  M.  Salikhov), as
well as the spin-label method [92-97] (Fig. 6).
Experimental work in chemical kinetics started
by V.  V.  Voevodsky’s group at the same Institute in
mid-1950s was continued by his students, after he
(and a considerable number of his colleagues) left in
1961 for the newly established Institute of Chemical
Kinetics and Combustion in Novosibirsk. The range
of studies carried out by Voevodsky and later by his
students included absorption and heterogeneous catal-
ysis [98-101], free-radical reactions in the solid state
[102, 103], EPR studies of the structure of substanc-
es, and publishing of the Atlas (chart) of the EPR
Spectra [104, 105], among other things. Recognizing
limitations of the EPR method in the “common” ul-
trahigh-frequency range (3
cm, 8 mm), Y.  S.  Lebedev
FIRST DECADES IN THE SOVIET UNION S455
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
would eventually create a new field in EPR spectros-
copy – high field electron paramagnetic resonance
[106, 107] – and supervise the development of the
first D-band (2 mm) EPR spectrometer (it went as far
as into small series production in the USSR) [108].
In the early period (late 1950s-early 1960s), NMR
spectroscopy investigations at the Institute for Chem-
ical Physics were the domain of L. L.  Dekabrun’s
Laboratory [109]. L.  L.  Dekabrun himself was for the
most part concerned with the development of NMR
spectroscopic tools [110-112] (Fig.
7). In this he ad-
vanced as far as it was possible in such a complex
field as high-resolution NMR and in the context of
the USSR mass production standards (more on this
in Scientific Instrumentation for EPR and NMR Spec-
troscopy in the USSR later in this Chapter). Roughly
in the same period, NMR spectroscopy as a method
for chemical research was studied by his fellow col-
leagues in Moscow and at the Institute’s branch in
Chernogolovka
26
[113-114].
The findings obtained by the young theoretical
chemists of the Theoretical Department and of the
Quantum Chemistry Lab at the Institute of Chemical
Physics (I.  V.  Alexandrov, N.  N.  Korst, E.  E.  Nikitin,
B.  N.  Provotorov, T.  N.  Khazanovich, and their stu-
dents) would later become classic for the theory of
paramagnetic relaxation. B.  N.  Provotorov, for exam-
ple, suggested a theory of two energy reservoirs cre-
ated by cross relaxation (similar to the Zeeman and
spin–spin reservoirs).
After the Institute of Chemical Physics had grown
to set up a branch in Chernogolovka, this science town
near Moscow became another center for magnetic res-
onance research. By the beginning of 1970s, the resi-
dent researchers of the branch’s labs (I.  F.  Schegolev,
I.  S.  Krainsky, V.  A.  Zabrodin, G.  V.  Lagodzinskaya)
and engineering workshops (V.  K.  Enman and oth-
ers) had designed and built high-field NMR spec-
trometers using superconducting solenoids, the only
of their kind in the USSR. They were a 180  MHz
NMR spectrometer manufactured in 1970 and a
294  MHz NMR spectrometer that went into production
in 1974 [115,  116]. A double NMR spectrometer and
a solid-state NMR spectrometer were developed by
L.  N.  Erofeev at G.  B.  Manelis’ laboratory. Theoretical
research (B.  N.  Provotorov, E.  B.  Feldman) “moved” to
Chernogolovka in mid-1970s as well.
In 1960s, NMR spectroscopy was adopted as an
indispensable research method by many of the chem-
ical institutes in Moscow, such as: Zelinsky Institute
of Organic Chemistry, the Institute of Organoelement
Compounds and the Institute of Fossil Fuels of the
USSR Academy of Sciences, Karpov Research Insti-
tute of Physical Chemistry, etc. At the Institute of
Organic Chemistry, for example, its Special Design
Bureau had a dedicated NMR Department that em-
ployed outstanding Soviet instrumentation designers
A.  N.  Lyubimov and A.  F.  Varenik. The Institute of Or-
ganoelement Compounds had a strong group of NMR
experts (E.  I.  Fedin, P.  V.  Petrovsky, I.  P.  Amiton et al.)
working at its Laboratory of Structural Analysis led by
A.  I.  Kitaigorosky. A.  N.  Nesmeyanov, Director of the
Institute, who was also head of the Department of Or-
ganic Chemistry at Lomonosov Moscow State Universi-
ty, established the NMR spectroscopy group, later-labo-
ratory, there as well, originally studying, for the most
part, metal-organic compounds [117]. At Lomonosov
Moscow State University, NMR spectroscopy in chem-
istry research had another advocate in A.  V.  Kiselev,
Professor, Department of Physical Chemistry.
After the political controversy over the reso-
nance theory in the USSR had ended, Y.  K.  Syrkin and
M.  E.  Dyatkina returned to their EPR studies they had
to pause for nearly a decade, at Kurnakov Institute
of General and Inorganic Chemistry and at Moscow
Institute of Fine Chemical Technology. Their research,
after 1959, was mostly focused on studying metal-
organic compounds [118, 119].
EPR spectroscopy in biology. ‘EPR in Biology’ in
the USSR started with L.  A.  Blumenfeld [29,30], whose
works published in 1957 prompted a rapid growth of
EPR spectroscopy applications in biological research.
A.  F.  Vanin, his student, was the first to detect nitric
oxide in biological tissues [120]; in 1998, discoveries
concerning the role of nitric oxide as a signaling mol-
ecule in cardiovascular system would win the Nobel
Prize in Physiology or Medicine. The double electron–
electron resonance [121] discovered by Blumenfeld’s
group, completely independently but simultaneously
with J.  Hyde [122], was a breakthrough in the field
as well. Studies of bioenergy processes was another
significant line of research conducted by Blumenfeld
and his students E.  K.  Ruuge, A.  N.  Tikhonov and oth-
ers [123, 124] (Fig.8). Eventually, Blumenfeld’s exper-
imental work developed into a strong school of bio-
physics, the range of problems it covered going well
beyond EPR studies in biology [125, 126].
In the beginning of the 1960s, EPR investigations
in physiology and medicine were launched at the
Institute of Biological Physics
27
of the Soviet Acade-
my of Sciences in Moscow, and later in Pushchino
28
.
Its scope of research covered the structure [127]
26
A science town (naukograd) in the Moscow Region (Oblast).
27
Now the Institute of Theoretical and Experimental Biophysics and the Institute of Cell Biophysics of the Russian
Academy of Sciences.
28
A science town in the Moscow Region, the Research Center for Biological Studies of the Russia Academy of Sciences.
KESSENIKH, PTUSHENKOS456
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig.  8. A. F.  Vanin (left), L.  Berliner (center) and A.  N. Tikhonov (right) at the IX EPR Workshop on EPR in Biology and
Medicine, Krakow, 2013. Source: personal archive of A.  F.  Vanin.
Fig. 9. M.  A. Ostrovsky (right) and his teacher, physiologist V.  G.  Samsonova (2nd left), early 1960s. Source: personal archive
of M.  A. Ostrovsky.
and function of myosin [128], respiration and oxida-
tive phosphorylation [129], and other problems. One
of the most interesting and fruitful lines of investi-
gations pertained to the photobiophysics of retinal
function was studied by M.  A.  Ostrovsky (the Institute
of Higher Nervous Activity and Neurophysiology of
the USSR Academy of Sciences) in cooperation with
L.  P.  Kayushin (the Institute of Biological Physics) very
early in the 1960s [130, 131]. Basically, they were the
first in the world to study photoreception using the
EPR method. Following their early findings, M.  A.  Os-
trovsky suggested that the retinal pigment epithelium,
previously considered as a neutral density filter in the
optic cup passively absorbing scattered light, might
in fact be instrumental in visual photoreception [132,
133]. In the end, that and some other research grew
into a new field of scientific knowledge – molecular
physiology of vision, of which M.  A.  Ostrovsky is ac-
knowledged one of the founders (Fig. 9).
In the same late 1950s, EPR studies of synthetic
polymers [134] were launched to be followed by EPR
studies of biological compounds [135, 136] at the De-
partment of Radiobiology of the Institute of Atomic
Energy of the USSR
29
. The idea apparently came from
V.  U.  Gavrilov, head of the Department. Primary focus
of the studies, at least in the beginning, was on the rad-
icals formed in a substance due to radiation exposure,
their composition, stability, and interactions [137].
29
Now Kurchatov Institute, National Research Center.
FIRST DECADES IN THE SOVIET UNION S457
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Leningrad: selected research. In Leningrad,
magnetic resonance spectroscopy studies had a rel-
atively early start – in the beginning of 1950s at the
latest. At the Leningrad State University, a magnet-
ic resonance Laboratory was set up by F.  I.  Skripov.
Back then, he began NMR investigations of the Earth’s
magnetic field [138], an ongoing research up to the
present day at now St.  Petersburg State University.
Interestingly, Skripov was de facto the first to apply
the Fourier transform technique to NMR spectroscopy
[139]. Yet, priority of the discovery was lost due to
resistance of the Soviet patent office to patent this
method, a frustratingly typical storyline in the histo-
ry of the Soviet science [140]. Nearly a decade later,
in 1966, a similar method would be independently
developed by R.  Ernst. Another research avenue Skri-
pov had been exploring was high-resolution NMR
spectroscopy [141]. In the early 1960s, acoustic NMR
studies were launched at the University as well by
V.  A.  Shutilov and his students [142-144].
Late in 1950s, at the Leningrad Physical-Techni-
cal Institute
30
EPR spectroscopy was applied to the
studies of free atoms trapped in polar and nonpolar
media [145, 146] along with experimental work with
regards to optical methods of atomic orientation (the
“optical pumping” method) [147]. Eventually, each de-
veloped into a whole new field of scientific research:
EPR studies of conductors and optically detected mag-
netic resonance (ODMR). In both, the now Ioffe Insti-
tute is among the leaders [148, 149].
Magnetic resonance instrumentation design was
another magnetic resonance-related area that had a
relatively early start in Leningrad. It began in 1960 at
the Special Design Department for Analytical Instru-
mentation (SDD AI) of the USSR Academy of Sciences,
with Leningrad Electrotechnical University
31
launch-
ing a similar program later (more on this in Scientif-
ic Instrumentation for EPR and NMR Spectroscopy in
the USSR later in this Chapter).
Minsk: school of EPR spectroscopy. In Minsk,
the history of EPR studies began in 1956 after
M.  A.  Elyashevich left the Institute of Chemical Phys-
ics (USSR Academy of Sciences) in Moscow for the Be-
larusian State University. As was said earlier, in the
USSR, application of EPR and to some extent NMR, as
a method for studies in biology and in chemistry start-
ed at the Institute of Chemical Physics. In mid-1950s,
potential of the resonance methods in those fields was
widely discussed there, and Elyashevich was among
the most enthusiastic advocates of the technique [150].
In the next decades, the scientific school he founded
contributed a lot to the development of EPR applica-
tions in chemistry, geology, medicine, and in other
fields. But its major achievement was the develop-
ment of a new class of compact EPR spectrometers
prompting growth of EPR studies in the USSR in gen-
eral, in particular in the decade before the collapse of
the Soviet Union. Several generations of his students
stood behind those advancements in instrumentation
design with S.  S.  Shushkevich (in the 1960s-1970s) and
V.  N.  Linev (since mid-1970s) playing the crucial part
(Fig.4) [151]. Their designs are discussed in more de-
tail in the Scientific Instrumentation for EPR and NMR
Spectroscopy in the USSR later in this Chapter.
Tallin: works on application of NMR spectros-
copy in chemistry by the group of E.  T.  Lippmaa. In
1962, another outstanding scientist and his group en-
tered the playing field of high-resolution NMR, joining
Dekabrun, Bystrov, and Samitov – Estonian chemical
physicist Endel Lippmaa of the Tallinn University of
Technology [152,  153]. By that time, Lippmaa had al-
ready left the University for the newly established In-
stitute of Cybernetics of the Estonian SSR Academy of
Sciences to head its Division of Physics; his group and
equipment following him to the Institute. He never
aimed to provide the Soviet industry with a prototype
for serial production of a proton magnetic resonance
(PMR) spectrometer. Having mastered the PMR method
(proton–proton double resonance included), Lippmaa
rather aspired to use spectroscopy in the studies of
the
13
C isotope, a carbon essential in organic chemis-
try studies. To that end, special, much more sensitive
techniques (proton–carbon double resonance in par-
ticular) capable of massive data accumulation, were
required. Lippmaa found the solution in equipping
his spectrometers (there were at least four of them
by that time) with a computer-based add-on system
he managed to procure in Finland, and thus made his
laboratory one of the world leaders in
13
C,
15
N and,
since 1965,
14
N NMR spectroscopy [154, 155].
Kiev and Kharkov: acoustic resonance studies.
In 1957, at the Institute of Physics, Academy of Sci-
ences, Ukrainian SSR, Kiev, M.  F.  Deigen launched his
radiospectroscopic studies of nonmetallic crystals that
were later scaled up at the Department of Radio Spec-
troscopy he created at the Institute of Semiconduc-
tors, Academy of Sciences, Ukrainian SSR, that spun
off the Institute of Physics in 1960. Deigen’s focus was
to a great extent on the development of the electron
nuclear double resonance (ENDOR) method, which he
recognized as a remarkably informative and potent.
Under his guidance the first ENDOR apparatus in the
USSR was built and used to determine energy-band
structure and electron density distribution in crystals,
among other things. Deigen’s systematic research on
the influence of external factors (such as tempera-
30
Now the Ioffe Physical-Technical Institute of the Russian Academy of Sciences.
31
Now Saint Petersburg Electrotechnical University “LETI”.
KESSENIKH, PTUSHENKOS458
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
ture, pressure, electric fields, etc.) on the EPR and
ENDOR spectra gave birth to a whole new field of
study – radiospectroscopic studies of material prop-
erties localized in the vicinity of defect sites [156].
His experimental work contributed to the refined theo-
ry explaining ENDOR frequencies, intensities, and line
shapes. Likewise, Deigen predicted the electron-nucle-
ar double magneto-acoustic resonance (ultrasound-
induced transitions between nuclear sublevels) to be
confirmed experimentally two years later [157].
In Kharkov, at the Institute of Radiophysics and
Electronics, Academy of Sciences, Ukrainian SSR
32
,
hypersonic studies were launched early in the 1960s,
acoustic paramagnetic resonance studies to follow
suit later [158, 159].
Tbilisi. In Georgia, magnetic resonance re-
search started with G.  R.  Khutsishvili, L.  D.  Landau’s
post-graduate student, coming to work to the Insti-
tute of Physics, Academy of Sciences, Georgian SSR, in
the early 1950s. By mid-1960s, there and at the Tbilisi
State University a strong group of theoretical physi-
cists was eventually brought together: G.  R.  Khutsish-
vili, L.  L.  Buishvili, M.  D.  Zviadadze, and others [160-
163]. At the Tbilisi University, T.  I.  Sanadze’s group
launched its EPR studies of polymers and crystals
[164, 165], investigations of a wide range of phe-
nomena to follow: forbidden transitions and magnet-
ic relaxation, line shapes and saturation effects, the
Overhauser effect, EPR, NMR, and FMR. Noteworthi-
ly, despite a thousand-mile distance between Tbilisi
or Tallinn and Moscow, scientific groups working in
the different parts of the Soviet Union collaborat-
ed closely, which is clear from the composition of
author teams and acknowledgments in some of the
papers.
Yerevan. EPR studies in Armenia were directly
related to similar research at the Institute of Chemi-
cal Physics in Moscow. In 1959, A.  B.  Nalbandyan – a
student of N.  N.  Semenov and, since 1960, a corre-
sponding member of the Academy of Sciences, Arme-
nian SSR (since 1963, an academician) – established a
Laboratory (later Institute) of Chemical Physics, Acad-
emy of Sciences, Armenian SSR, in Yerevan. Much of
his research stemmed from his earlier work in Mos-
cow [166] pertaining to combustion mechanisms [167-
170], in particular to the degenerate branching chain
reaction kinetics and mechanism. In addition to ERP
and laser magnetic resonance spectroscopy already
in use, a new technique – the rapid freezing method
to detect radicals – was developed and employed in
experimentation at the Laboratory. Strengths and lim-
itations of the three methods, along with the findings
obtained with their use, were later summarized in a
number of monographs [171, 172].
Molotov
33
: magnetic resonance spectroscopy.
In Perm, magnetic resonance related research start-
ed with I.  G.  Shaposhnikov. A person with an ex-
traordinary trajectory of life (Voronezh–Vladivostok–
Moscow–Vladivostok–Kazan–Nikolaev–Kazan–Perm
34
),
he crossed paths with E.  K.  Zavoisky at the turning
point in EPR history – at the time of the EPR discov-
ery. On his return from the front lines, Shaposhnikov,
for a short period of time (1945-1946), worked at the
Kazan State University, Department of Experimental
and Theoretical Physics headed by Zavoisky. Para-
magnetic relaxation was among the subject matters
he conducted studies on, according to the Depart-
ment’s report [4]. In 1946, he was appointed head of
the Department of Theoretical Physics that “seceded
from” the Zavoisky’s Department, and in 1948 – left
for Molotov State University
35
. Paramagnetic relax-
ation, however, continued to be a phenomenon of sci-
entific interest for him. After his Kazan-time research
[173-175], he returned to the related phenomena in
many of his later works [176-179].
Since the late 1950s, other researchers at Molotov
State University embarked on the studies of various
of magnetic resonance phenomena: EPR, NMR, NQR,
and related phenomena in crystals, gases, and biolog-
ical systems [180-184]. Similarly, development of in-
strumentation for magnetic resonance studies started
at the University in the same period, in particular of
instruments for the NQR and quadrupole spin echo
observation, NMR sensors, and tools for experiment
automation [185-187]. According to the recently pub-
lished collection of selected works by the scientists of
Perm State University [188], a great number of papers
came out within the decade (1960-1970). Unfortunate-
ly, for the most part, the research was originally pub-
lished in the local, not readily available, press, such
as: “Transactions of ENI
36
, Perm State University”,
“Transactions of Perm State University”, “Proceed-
ings of VUZes
37
”, “Radio Spectroscopy”, collections of
conference proceedings, etc. Too many scientists were
involved in magnetic resonance studies in Perm to
list all of them here. The most frequent names among
the authors of theoretical and experimental research
include: V.  S.  Grechishkin, N.  E.  Ainbinder, G.  B.  Soifer,
32
Now Usikov Institute for Radio Physics and Electronics of the National Academy of Sciences of Ukraine.
33
Now Perm.
34
Regional centers all across Russia and Ukraine.
35
Now Perm State University, also Perm State National Research University.
36
Transliterated abbreviation standing for the Institute of Natural Sciences.
37
Transliterated abbreviation standing for Higher Educations Establishments.
FIRST DECADES IN THE SOVIET UNION S459
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
I.  A.  Kuntsel, M.  L.  Zlatogorsky, and L.  M.  Tsirulnikova.
Among the developers, most frequently published
V.  P.  Zelenin, V.  A.  Kushkov, G.  I.  Subbotin, S.  I.  Guschin,
V.  A.  Shishkin, B.  G.  Derendyaev, Y.  I.  Rosenberg,
G.  G.  Kudymov, and Y.  G.  Svetlov.
Sverdlovsk
38
. In Sverdlovsk, a school of physics
of magnetic phenomena emerged already in 1940s,
driven mostly by S.  V.  Vonsovsky and his research (as
early as in 1948 his monumental work [189] was pub-
lished). It was no coincidence that the First All-Union
Conference on the Physics of Magnetic Phenomena
held in 1946, E.  K.  Zavoisky and B.  M.  Kozyrev invit-
ed, took place in Sverdlovsk. In mid-1950s, EPR, NMR,
and FMR studies began there too, carried out most-
ly at the Ural Polytechnic Institute
39
. The renowned
Urals school of magnetic resonance was eventually
established by G.  V.  Skrotsky [190-193], at the very
least it was strongly influenced by his work.
Apart from its scientific contribution, the Ural
school, or its leader G.  B.  Skrotsky to be precise, cre-
ated a valuable phenomenon of a different kind– the
All-Union Workshops on Magnetic Resonance held ev-
ery other year starting with 1968 all across the Soviet
Union. The Workshops attracted young (and not so
young) scientists from all over the USSR to share
knowledge and build working and friendly relation-
ships within the Soviet magnetic resonance commu-
nity.
Novosibirsk: school of EPR-spectroscopy
(V.  V.  Voevodsky school). In Novosibirsk, EPR and
NMR spectroscopy development is associated with
V.  V.  Voevodsky and his group, who was transferred
from the Institute of Chemical Physics, Moscow, to
the newly established Institute of Chemical Kinetics
and Combustion, USSR Academy of Sciences, Siberian
Branch. Although officially Voevodsky and his team
started working there in 1959, the Institute’s building
was still under construction at the time and thus in
actual fact they moved to Novosibirsk only two years
later, in 1961. That year was the starting point in the
history of magnetic resonance research in Novosibirsk
and a new stage in the development of Voevodsky’s
school of radio spectroscopy in chemistry. They never
lost touch with their Moscow colleagues, though, in
particular with those at the Institute of Chemical
Physics, and many of the works were carried out in
close cooperation.
In the decade discussed here (1961-1970), Vo-
evodsky and his colleagues continued EPR radiolysis
research they started back in Moscow in 1957 with
the launch of EPR spectroscopic studies using the In-
stitute’s electron beam accelerator. In Novosibirsk, the
scope of EPR research grew to include radical recom-
bination reactions and intramolecular energy transfer
[194-197], as well as combustion reactions involving
radical generation detectable by EPR spectroscopy [35,
198] (Fig.  10). Problems pertaining to photochemistry
[199], polymer chemistry [200], and catalysis [201]
had all been within the realm of scientific inquiry of
the new school of radiospectroscopy. In the biology
related research Voevodsky’s group was assisted by
the Institute of Cytology and Genetics, the USSR Acad-
emy of Sciences, Siberian Branch [202].
Another important avenue explored in Novo-
sibirsk pertained to the relaxation and spin echo
methods [203-207] including theoretical explanation
and interpretation of the spin echo experimental re-
sults. Theoreticians at the Institute of Chemical Ki-
netics and Combustion, K.  M.  Salikhov in particular,
contributed a lot to the advancement of the theory
of exchange interactions, the theory of spin waves,
and other theoretical problems [208-211]. Finally, in
the same period, spin chemistry, a new field of study
that would burgeon in the next decade, was already
emerging in the works of the scientists in Novosi-
birsk [212] (Fig. 11).
NMR spectroscopic studies in chemistry were
advancing in Novosibirsk along with the EPR re-
search, including those regarding biophysical prob-
lems [213], such as studying structures of glycosides
from Ginseng, denaturation of tRNAs [214, 215].
38
Now Ekaterinburg.
39
Now part of the Ural Federal University named after the First President of Russia B. N. Yeltsin.
Fig.  10. Yu. N.  Molin (left) and Yu.  D.  Tsvetkov (right), No-
vosibirsk, 1962. Source: the Electronic Photo Archive of the
Siberian Branch of the Russian Academy of Sciences, http://
www.soran1957.ru/?id=krai_100616111436_2725_0. Courtesy
of I.  Yu. Pavlovskaya.
KESSENIKH, PTUSHENKOS460
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 11. K.  M. Salikhov (left), R.  Z.  Sagdeev (2nd left), Yu. N.  Molin (right), Novosibirsk, 1989. Source: personal archive of
Yu.  N. Molin.
A standalone comparative research was launched
to study correlation between the findings obtained
in both methods [216]. In the same years, spin la-
belling (iminoxyl radicals) was being researched
[217, 218]. Continuing their cooperation with the In-
stitute of Chemical Physics, Voevodsky’s group was
part of the “exotic” positronium studies carried out
by V.  I.  Goldansky.
It must be said that another center for NMR stud-
ies emerged in Novosibirsk later in the same period
the Institute of Organic Chemistry, USSR Academy of
Science, Siberian Branch
40
, EPR research eventually
added to its scientific agenda as well.
Krasnoyarsk: NMR spectroscopy. Krasnoyarsk’s
school of NMR spectroscopy was founded by A.  G.  Lun-
din – one the few who passed Landau’s Theoretical
Minimum
41
, alumnus of Moscow Power Engineering
Institute and of the Institute of Physical Problems, the
legendary “kapitsnik”, where he had been working
for three years. In 1950, amid the battle against cos-
mopolitism
42
gaining momentum in the USSR, he was
posted to Krasnoyarsk to the radio engineering plant.
There he spent the next 13 years. Lundin, however,
never surrendered to his “excommunication” from
the scientific work and, in 1951 decided to conduct
research, off work, at the Siberian Forestry Engi-
neering Institute
43
, Department of Physic, headed by
P.  S.  Sarapkin, in cooperation with G.  M.  Mikhailov.
The NMR method, he developed a strong interest for
back at the “kapitsnik”, was his field of choice for the
studies he embarked on in Krasnoyarsk. Supported
by L.  V.  Kirensky, a friend of P.  S.  Sarapkin, Lundin
was well equipped to make quick progress in his
experiments. By the year 1957, A.  G.  Lundin and his
colleagues had built an NMR spectrometer using a ro-
tating magnet (placed on an anti-aircraft gun mount)
to investigate effects of crystal orientation [219].
In 1963, after 13 years at the radio engineering plant,
A.  G.  Lundin was offered a position at the Institute of
Physics, USSR Academy of Sciences, Siberian Branch,
by L.  V.  Kirensky. Since that year the Institute of
Physics had been the heart of NMR research in Kras-
noyarsk.
Lundin’s school focused predominantly on NMR
investigations of crystals: crystalline hydrates, organic
acids crystals, minerals, etc. [220, 221]. Worth partic-
ular mention are the studies of ferroelectric phase
transitions and of the nature of ferroelectricity [222-
224]. On the theoretical side, effects of internal mo-
lecular motions in NMR spectra [225, 226] were inves-
tigated, as well as an approach was developed to the
line-shape inverse problem in the NMR spectra, that
is to determination of the crystal cell parameters by
means of orientation-dependent spectra [227].
Although as early as in 1964 the Institute of
Physics somehow got hold of a brand-name Japan
40
Now the N.  N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Russian Academy of Sciences, Siberian
Branch.
41
Landau developed a comprehensive exam called the “Theoretical Minimum” which students were expected to
pass before admission to his seminar. The exam covered all aspects of theoretical physics. Between 1934 and 1961
only 43 candidates passed.
42
An euphemism for the anti-Semitic campaign in the USSR waged in 1948-1953.
43
Now part of Reshetnev Siberian State University of Science and Technology.
FIRST DECADES IN THE SOVIET UNION S461
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
NMR spectrometer JNM-3H-60, experimental instru-
mentation was, for the most part, assembled at the
Institute itself, including by the Lundin’s team. For
example, for the studies of solids, they built a wide-
line NMR spectrometer using a superconducting mag-
net (NMR-213M
44
), one of the most impressive strides
made by Lundin and his colleagues in spectroscopic
instrumentation. It would later go into a small-series
production (more on this in Scientific Instrumenta-
tion for EPR and NMR Spectroscopy in the USSR lat-
er in this Chapter). Apart from this major piece of
equipment, Lundin’s team designed and built a great
many of simpler tools, such as high-temperature sen-
sors for NMR spectroscopy, instruments for record-
ing spectra at high hydrostatic pressures, automation
tools for processing NMR spectra, and experiment
automation systems. New methods, including pulsed
NMR [228], were advancing as well. In the domain
of EPR instrumentation, a Q-band (8 mm) EPR spec-
trometer capable of applying uniaxial pressure to
the sample was developed, along with the set of EPR
magnetometers (EPRAN-1200) for geophysical mea-
surements (E.  P.  Zeer, G.  F.  Lybzikov, V.  V.  Menshikov,
S.  A.  Trofimov, V.  V.  Lisin et al.), although it was in
the later years – in the second half of the 1970s.
SCIENTIFIC INSTRUMENTATION FOR EPR
AND NMR SPECTROSCOPY IN THE USSR
Rapid development of radiospectroscopic stud-
ies in chemistry and biology, as was said earlier,
began with the groups led by V.  V.  Voevodsky and
L.  A.  Blumenfeld launching their research at the In-
stitute of Chemical Studies, USSR Academy of Scienc-
es, in mid-1950s. Voevodsky’s group meanwhile con-
tributed to yet another breakthrough in the field of
EPR instrumentation design, owing mostly to the ef-
forts of his younger colleagues, namely N.  N.  Bubnov,
Y.  N.  Molin, A.  G.  Semenov, Y.  D.  Tsvetkov (Fig.  10),
and V.  M.  Chibrikin [229]. As a result of extended
enough collective efforts, A.  G.  Semenov developed
an original spectrometer that came to be known as
EPR-2
45
spectrometer. Its design allowed to study
free-radical reactions with high precision (resulting
from the use of a transmission-type resonator, a dou-
ble-modulation technique, and a tunable frequency
oscillator [230]). To a certain extent, EPR-2 spectrom-
eter filled the void of the Soviet original instrumen-
tation for the years to come. Using EPR-2 as a proto-
type, Leningrad Special Design Bureau for Analytical
Instrumentation, USSR Academy of Sciences, designed
a model optimized for mass production. It had been
on the market for the next 15 years (up to 1976) as
a RE1301
46
spectrometer produced by the Smolensk
Plant of Automation Equipment [231]. Studies using
ERP spectroscopy grew in number as new scientif-
ic institutions were established on the wave of the
so called “Big Chemistry”
47
program, namely, in the
Institute of Chemical Kinetics and Combustion in No-
vosibirsk and the Branch of the Institute of Chemical
Physics in Chernogolovka. The Institute of Chemical
Physics itself continued to widely use the EPR meth-
od in its research. Quality of the instrumentation
manufactured in the USSR, no doubt, had room for
improvement. G.  I.  Likhtenshtein [232], for example,
reminisced how academician A.  L.  Buchachenko had
to fine-tune his manufactured RE1301 himself. The
important thing though was that there were EPR in-
struments produced in the USSR. As there was orig-
inal literature on the EPR methods published in the
Soviet Union, especially so in the early 1960s (more
on this in Chapter IV, part II).
In the context of EPR instrumentation develop-
ment in general, though, one must say that in the lat-
er years progress was rather modest. Considering the
scientific-technological revolution in the world, sci-
entific instrumentation engineering in the USSR was,
alas, behind the knowledge-intensive industries in
the West. New instruments, however, continued to be
developed. The Special Design Bureau for Analytical
Instrumentation, for example, in the 1960s-1970s de-
signed a series of EPR spectrometers of the RE
48
-fami-
ly, both the traditional 3-cm instruments (X-band), and
8-mm models (Q-band). The RE family of spectrome-
ters was the most common in the USSR: several hun-
dred of them were manufactured over two decades
(early  1960s-mid-1980s). Along with the RE spectrom-
eters, more advanced instruments were designed and
produced in small series. Of them the most common-
ly known was the EPR-3 (Siberia)
49
spectrometer de-
veloped by A.  G.  Semenov at the Institute of Chemical
Kinetics and Combustion, USSR Academy of Scienc-
es, Siberian Branch, in Novosibirsk. It was manufac-
tured by the Pilot Plant, USSR Academy of Sciences,
Siberian Branch, as a small series of 45 instruments.
44
In Cyrillic, ЯМР-213М.
45
In Cyrillic, ЭПР-2.
46
In Cyrillic, РЭ1301.
47
A large-scale program announced by the USSR government to develop chemical industry in the country for the years
1959-1980.
48
In Cyrillic, РЭ.
49
In Cyrillic, ЭПР-3 “Сибирь”.
KESSENIKH, PTUSHENKOS462
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 12. Specialized compact EPR spectrometer constructed by V.  N.  Linev’s team at BSU early in the 1980s. Source: personal
archive of V.  N. Linev.
At the same Institute, Y.  D.  Tsvetkov designed a pulsed
EPR spectrometer, although it failed to go into pro-
duction. Y.  S.  Lebedev’s laboratory at the Institute of
Chemical Physics, Moscow, was another player in the
field of EPR instrumentation development. In coop-
eration with the Donetsk Institute for Physics and
Engineering, Academy of Sciences, Ukrainian SSR,
Lebedev’s team designed the first high-field (2-mm)
spectrometer in the USSR. Also involved in the de-
velopment of special purpose EPR spectrometers was
Ulyanov Leningrad Electrotechnical Institute (LETI).
Small series of the LETI’s spectrometers were pro-
duced by the Leningrad Association of Electronic In-
strumentation “Svetlana”, USSR’s famous electronic
instrumentation manufacturer.
In the latest years of the discussed period argu-
ably the most important, in terms of small series EPR
instrumentation production, was the development of
compact EPR spectrometers at the Belarusian State
University. The project was launched in mid-1970s
by S.  S.  Shushkevich, a student of A.  M.  Elyashevich,
who would eventually be thrown into the interna-
tional spotlight but in a totally different context
50
.
V.  N.  Linev was the central person in terms of devel-
opment as such. Eventually, he would be the one to
keep production of the benchtop EPR spectrometers
afloat amid the economical turmoil in the USSR and,
later, in independent Belarus. Back in 1970s, within
several years, he and his group developed extraor-
dinarily compact instruments weighing 28 to 50  kg.
Later, by introducing a permanent magnet instead of
a cumbersome electromagnet, spectrometer weight
was decreased down to 8  kg. To compare, a regu-
lar EPR spectrometer, including the spectrometers
of RE-family, weighed over a ton at the time in the
USSR. Compact size, lower power consumption, stron-
ger noise immunity and other parameters made Be-
larusian compact EPR spectrometers instrumentation
of choice in mineral exploration, manufacturing,
hospitals, etc. (Fig.  12) [151]. The Belarusian family
of benchtop EPR spectrometers is the only one that
survived the USSR and is still on the market, under
the brand name LINEV, former Adani.
In the development of NMR instrumentation,
meanwhile, the situation was much more complicat-
ed. Early in 1960s, literature on NMR (mostly by non-
USSR authors) only began to be published. Although
after 1955 restrictions on international contacts for
the Soviet scientists were eased, an international
exchange program was still an impossible dream at
the time. There was a huge void of NMR instruments
in the country. Attempts that were made to set up
manufacturing of NMR instrumentation all but failed.
While the Academy’s Special Design Bureau succeed-
ed in designing a basic EPR spectrometer suited for
production, it was still an impossible undertaking for
the USSR non-military industry to generate a strato-
spheric by its standards stability of magnetic field
and frequency, and magnetic field homogeneity (10
−8
).
The first designs developed by the Special Design Bu-
reau offered the ratio of 10
−5
, which was enough for
conducting some studies of broadened lines in solids.
The resulting prototype though was cumbersome, ex-
pensive, and, basically, useless for chemistry labs.
50
In 1991-1994, S. S. Shushkevich was Chairman of the Supreme Soviet of Belarus, the first head of state after Belarus
seceded from the Soviet Union. He was one of the three leaders who in December, 1991, signed the Belovezha Accords
that ended the USSR and established the CIS as a successor entity.
FIRST DECADES IN THE SOVIET UNION S463
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
As early as in the beginning of 1960s, there were
other endeavors to develop NMR spectrometers and
put them into small-series production, apart from
the “model range” designed by the Academy’s Special
Design Bureau. By 1961, L.  L.  Dekabrun’s lab at the
Institute of Chemical Physics had designed an NMR
spectrometer operating at 27 MHz proton frequency
[110]. Two years later, in 1963, it was used as a pro-
totype by the Design Bureau, Academy of Sciences,
Estonian SSR (headed by Enno Laud), to produce sev-
eral prototype samples of the SNMR-63
51
spectrome-
ter using a 0.5  T permanent magnet, for NMR studies
of
1
H and 
19
F. Karpov Institute of Physical Chemistry
in Moscow was among the reputable scientific institu-
tions that had been using the SNMR-63 spectrometer
for many years in its experimental work. Simultane-
ously, a 27  MHz proton NMR spectrometer was devel-
oped by Y.  Y.  Samitov of the Kazan State University.
Named KGU-1
52
, the Kazan spectrometer was used
by some institutions of the USSR chemistry industry.
It was a godsend to the Soviet NMR spectrosco-
py that M.  B.  Neiman, a pioneer of EPR in chemistry,
found two accomplished experts in building magnets
and electronic instruments in the depths of a Design
Bureau of the USSR Ministry of Ferrous Metallurgy,
one of the Soviet Union’s “sharashkas”
53
. They were
Alexander Nikolayevich Lubimov and Anatoly Fedo-
seevich Varenik, both political prisoners. Out of their
cooperation came the development of an almost up to
date NMR spectrometer (CLA 5535
54
, later RS-60
55
),
although it still was some 5 years behind its Western
analogues. The endeavor was described by E.  I.  Fedin
(Fig. 13) in his memoirs [233] and by I.  Y.  Slonim
[234] in his interview, among others. Success of
Lubimov and Varenik was based on the principle of
stabilization of gyromagnetic ratio with the help of
an auxiliary NMR signal. This was accompanied with
the impeccable mechanical and thermal processing
(in the reducing atmosphere) of the magnet pole tips.
With their CLA 5535 model Lubimov and Varenik dis-
pelled the myth about the Western instrumentation
designers forging magnet poles from the monocrys-
talline iron, a desperate idea once suggested by the
participants of N.  M.  Ievskaya’s NMR seminar at the
Moscow State University. E.  I.  Fedin, who worked di-
rectly with A.  N.  Nesmeyanov (Fig.  13), President of
the USSR Academy of Sciences in 1951-1961, initiat-
ed a campaign in support of Lubimov and his group
and against the conventional approach to NMR in-
struments design adopted by the Special Design Bu-
reau of the USSR Academy of Science. This essentially
a tragicomic story stemming from an article in the
Literaturnaia Gazeta (Literature Newspaper) in 1963
[235], was told in the Fedin’s memoirs and in the
recent article [236]. Following the outrage expressed
by the leadership of the Special Design Bureau, Erlen
Ilyich Fedin had to act as a mediator between the dif-
ferent members of the budding NMR instrumentation
industry. To some extent, he succeeded in his mission.
By 1966, both the Special Design Bureau of Analytical
Instrumentation in Leningrad (headed by Y.  K.  Klei-
man) and the Special Design Bureau of the Institute
of Organic Chemistry, USSR Academy of Sciences, in
Moscow had designed more or less adequate pro-
totypes of the 60 MHz proton NMR spectrometers.
(It was the latter institution that the Lubimov’s
group was eventually transferred to with the help
of Fedin.) The prototype designed in Leningrad was
put into production at the Smolensk Plant of Automa-
tion Equipment, while Lubimov’s design was manu-
factured at the Instrumentation Engineering Plant in
Sumy, Ukrainian SSR, as the RS-60
56
model. Unfortu-
nately, as experience showed, none of the two were
fully equipped to manufacture such an intricate in-
strument. Both manufacturers barely scraped through
with a total of two dozen instruments produced, and
only a few of them were used in real chemistry re-
search after being fine-tuned.
By 1974, E.  P.  Zeer from the Lundin’s lab at the
Institute of Physics in Krasnoyarsk had developed a
wide-line solid-state NMR spectrometer using a su-
perconducting solenoid (designed by A.  G.  Lundin,
E.  P.  Zeer, G.  F.  Lybzikov, V.  V.  Menshikov, Y.  A.  Zag-
orodny, and V.  A.  Babaev, with E.  P.  Zeer as a head
of the development group). In 1974, the spectrometer
was for the first time exhibited at VDNH
57
, USSR’s
biggest trade show. In 1975, after major improve-
ments, it was put on display in Leipzig, East Germa-
ny, where the International Autumn NMR Workshop
was being held [228]. In 1976, it was once again
51
In Cyrillic, СЯМР-63.
52
In Cyrillic, КГУ-1, an abbreviation standing for Kazan State University.
53
Secret research and development facilities operating through the work of prisoners within the Soviet Gulag labor
camp system and beyond under the supervision of NKVD, the Soviet secret service, from 1930 to the 1950s.
54
In Cyrillic, ЦЛА 5535.
55
In Cyrillic, РС-60.
56
In Cyrillic, РС-60.
57
A transliterated Cyrillic abbreviation standing for the Exhibition of Achievements of National Economy. A permanent
trade show and amusement park in Moscow, USSR (now in Russia), designed to demonstrate the best accomplishments
of Soviet industries.
KESSENIKH, PTUSHENKOS464
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 13. Left to right: E.  I. Fedin, A. N.  Nesmeyanov, and P.  V.  Petrovsky. The Institute of Organoelement Compounds, Moscow,
early 1970s. Source: personal archive of I.  P.  Amiton.
displayed at VDNH and this time was awarded gold-
en, silver, and three bronze medals. A.  G.  Lundin
was friends with E.  I.  Fedin, head of the Commission
for Radio-Frequency Spectroscopy, USSR Academy of
Sciences. Fedin’s former colleague at the Institute of
Organoelement Compounds, L.  A.  Fyodorov, was at
the time deputy for science at the Department of
Science Instrumentation, USSR Academy of Sciences.
Not least because of those friendships and enthusi-
asm on the part of Lundin and Fedin the Department
approved manufacturing of a small-series of NMR
spectrometers designed in Krasnoyarsk, at the Ex-
perimental Factory of Scientific Engineering in Cher-
nogolovka. Within several years, 10 spectrometers
were produced under the brand-name NMR-213M
58
.
Finally, in the late 1970s-early 1980s, the Acad-
emy’s Special Design Bureau made an effort to set
up mass-production of a high-field NMR spectrome-
ter. According to the Bureau itself, it “had been en-
tertaining the idea of developing a radio-frequency
spectrometer with a superconducting magnet since
the early seventies, but for various reasons could not
move ahead before 1979” [231]. In 1979, encouraged
by the enthusiasm of E.  I.  Fedin, head of the Acade-
my’s Commission for Radio-Frequency Spectroscopy,
the Bureau proceeded with the development of such
instrument. The high-resolution laboratory NMR spec-
trometer designed by I.  F.  Schegolev, I.  S.  Krainsky,
V.  A.  Zabrodin, G.  V.  Lagodzinskaya, V.  K.  Enman etal.
at the Institute of Chemical Physics, Chernogolovka
Branch was used as a starting point (Fig.  14). By1982,
the Bureau had “finished building its RI2304
59
mod-
el – a pulsed-Fourier-transform
1
H NMR spectrom-
eter with a superconducting magnet, operating at
200MHz, the first in the USSR” [231]. Alas, the instru-
ment missed its chance to be put into production. In
1982, the Smolensk Scientific Development and Pro-
duction Center “Analitpribor”. suspended its magnetic
resonance instruments production, while MicroInstru-
mentation Plant in Lviv, Ukrainian SSR, was not to
start manufacturing MR instrumentation until several
years later. Moreover, production of the RI2304 model
required stronger technical capabilities than those of
the EPR or NMR spectrometers manufactured before,
which was out of reach for any of the two plants.
Meanwhile, Soviet chemists had been growing to
understand that foreign instrumentation had to be
employed. The first were the chemists of the Acade-
my’s Institute of Macromolecular Compounds in Len-
ingrad who, in 1960, acquired a Japan 40  MHz PMR
spectrometer. In 1961, two 25  MHz NMR spectrome-
ters manufactured by Trüb, Täuber &Co, Switzerland,
were acquired– one by the Karpov Institute of Physi-
cal Chemistry, the leading scientific institution of the
USSR chemical industry, and the other by the Institute
of Organoelement Compounds headed by the presi-
dent of the USSR Academy of Sciences A.  N.  Nesmey-
anov. Structural studies of organic and organo-
element compounds with the use of the imported
instruments produced some results, providing basis
58
In Cyrillic, ЯМР-213М.
59
In Cyrillic, РИ2304.
FIRST DECADES IN THE SOVIET UNION S465
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
Fig. 14. The first prototype of the ChG-180 MHz NMR spectrometer developed in Chernogolovka in 1971(a) and its authors
V.  P.  Bubnov, G.  V.  Lagodzinskaya, and V.  A.  Zabrodin, after the instrument was made ready to be transferred to the museum,
2006 (b). The intended transfer, however, fell apart in the end. Source: personal archive of G.  V.  Lagodzinskaya.
for a meaningful discussion with the Western peers
for whom NMR spectroscopy was already an integral
part of their research work. Practical experience with
the Trüb–Täuber spectrometers using a permanent
magnet made it clear that, given technical capabili-
ty of the USSR instrumentation industry at the time,
endeavors to build a decent permanent-magnet PMR
spectrometer would have been a lost cause. Magnetic
induction below 2  T was sufficient to provide neither
the necessary sensitivity nor the resolution required
for proton resonance in organic compounds (due to
specific characteristics of proton spectra, indirect
spin–spin interactions– at low PMR frequencies– of-
ten being of the same order of magnitude as chem-
ical shifts). In fluorine NMR, though, magnetic fields
of such a strength were at least in some instances
operative. Foreign instrumentation thus made its way
into the budgets of USSR leading chemistry research-
ers. In the West, Japan JEOL spectrometers could
not compete with the ones manufactured by the US
Varian Associates with its instruments based on the
Bloch–Hansen patented technology and laboratories
employing the best of the US NMR experts. Despite
the US embargo on strategic materials, equipment,
and arms exports to the USSR
60
, JEOL spectrometers
were shipped to the Soviet Union to be used by sci-
entific institutions of the Academy of Sciences, such
as Lomonosov Moscow State University (Y.  A.  Ustynuk
and N.  M.  Sergeev, Faculty of Chemistry), some of the
Institutes of the defense industry, and some of the
medical research facilities. The funds allocated to
Techsnabexport, a Soviet technology export and im-
port bureau, for purchasing spectroscopy instrumen-
tation most likely came from the oil export revenues.
The first Japan 100  MHz PMR spectrometers were
purchased for the Faculty of Chemistry of Lomonosov
Moscow State University and for the Institute of Mo-
lecular Biology, the USSR Academy of Science.
Since late 1960, it had been in the air that a
new era in the magnetic resonance development was
about to begin. The USSR was no exception – mag-
netic resonance research in the country reached a
turning point. In terms of theoretical studies, Sovi-
et scientists were on equal grounds as their West-
ern colleagues, and in some respects ahead of them
(B.  N.  Provotorov of the Institute of Chemical Physics,
with his theory of cross relaxation, and his students
M.  A.  Kozhushner and O.  I.  Olkhov; M.  I.  Rodak of
the Radio Engineering and Electronics Institute, USSR
Academy of Sciences; theoreticians of the Tbilisi State
University). In experimental instrumentation develop-
ment, however, the Soviet Union was frustratingly be-
hind the West. Although, the EPR saturation studies
on dynamic nuclear polarization in crystals and poly-
mers did bear fruit. De facto, the USSR physicists dis-
covered the multi-particle method of dynamic nuclear
60
US Export Control Act of 1949. Under pressure from the US, the embargo was joined by 17 other countries, US allies,
including Japan.
KESSENIKH, PTUSHENKOS466
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
polarization (DNP) (V.  A.  Atsarkin, A.  E.  Mefed, et al.
of the Radio Engineering and Electronics Institute;
V.  I.  Luschikov, Y.  V.  Taran et al. of the Joint Institute
for Nuclear Research, who completed an apprentice-
ship at the A.  A.  Manenkov’s lab at the Physical Tech-
nical Institute). Following their international counter-
parts and drawing on the experimental findings by
Manenkov’s laboratory, Soviet physicists at the Joint
Institute for Nuclear Research developed a polarized
proton target to investigate the effect of proton spin
on neutron beams. Yet, breakthroughs were few and
far between, the real problem – manufacturing of
NMR instrumentation for chemistry research – re-
maining unresolved.
The new era in magnetic resonance development
came, firstly, with the emergence of pulse excitation
and Fourier transform techniques. New methods re-
quired every instrument to have a computer attached
to it to program the algorithm and collect the mea-
surements.
Secondly, it was the time of type II supercon-
ductors with high enough critical magnetic fields
to obtain magnetic fields of 4  T or higher (at PMR
frequencies of 200  MHz and higher). Thirdly, vacu-
um tubes were becoming history, superconductors
gradually taking their place in electronic instrumen-
tation. Soviet instrumentation industry switched over
to superconducting components eventually, although
it took time. There were fruitful, yet cautious, en-
deavors to build original superconducting solenoids
(dubbed “supercons” by Soviet instrumentation de-
signers). The process of integrating computers and
the Fourier transform method into MR instrumenta-
tion was, however, stalling. Mainframe computer sys-
tems developed in the USSR were quite good until
theES
61
series, a Soviet analogue of IBM’s System/360,
that was basically strongly ‘advised’ to be used since
the early 1970s. Regardless, the mainframes were too
big, both in size and in power consumption, to be
used in NMR spectrometers. Personal computers, on
the other hand, would have been up to the task, but
for some reason they were all but prohibited in the
Soviet Union.
While the world’s scientific community was pre-
paring for the breakthrough in the magnetic reso-
nance instrumentation industry, the USSR found itself
not ready for this. Nonetheless, the explosive devel-
opment, of which the Soviet Union was hardly a part
of, proved to be of some use for its NMR instrumen-
tation conundrum, although indirectly.
In 1967, Endel Lippmaa became firmly estab-
lished as one the leading designers of NMR instrumen-
tation in the USSR and beyond. On May13, 1967, the
USSR Academy of Sciences, Division of General and
Industrial Chemistry, held a meeting on NMR spec-
troscopy at its Institute of Organic Chemistry. Among
the speakers there were E.  I.  Fedin, Y.  Y.  Samitov,
V.  F.  Bystrov, and E.  Lippmaa, papers by the latter
two standing out. The discussion led to a definitive
resolution – there was a growing need for foreign
instruments to be purchased. By this time, foreign
companies such as Varian Associates and emerging
Bruker-Physik AG, coincidentally, had grown ready to
bypass the US embargo on electronic instrumentation
exports to the USSR that proved detrimental to busi-
ness (previously, only Finland and Japan had taken
the risk of ignoring the embargo).
In the summer of 1967, Varian Associates show-
cased its instruments in Moscow. Right from the
trade show the long-awaited 60  MHz and 100  MHz
PMR spectrometers equipped with add-ons for other
nuclei (fluorine, phosphorus), NMR stabilizer, and a
magnetic field inhomogeneity correction (shim) sys-
tem were shipped to the Academy’s institutions. Only
they missed  (!) computer add-ons and the Fourier
transform. Basically, Varian get rid of the outdated
instrumentation. Bruker-Physik AG chose to pursue a
different strategy. Right from the beginning, Bruker
offered Fourier transform spectrometers to its cus-
tomers in the USSR, operating at 90MHz instead of
100MHz but suitable for
13
CNMR spectroscopy. This,
however, would be a later development that would
take place in a year or two after the Varian’s trade
show. When it did, Varian Associates had to defy the
US embargo with regard to Fourier transform spec-
trometers as well, including the
13
C NMR instruments.
In the period of 1967-1969, the Soviet magnetic
resonance community finally consolidated. In Septem-
ber 1967, the All-Union Symposium on Nuclear Mag-
netic Resonance was held in Tallinn, Estonian SSR.
At the time, Lippmaa’s laboratory was the only one
in the Soviet Union equipped to collect
13
C spectral
data that, according to Lippmaa himself, “was im-
possible to be collected even by means of the fine
instruments purchased by the institutes in Moscow
and Novosibirsk.”
In 1968, in Sevastopol, Ukrainian SSR, the First
All-Union Workshop on Magnetic Resonance – a proj-
ect of G.  V.  Skrotsky, leader of the Urals school – was
held under the aegis of Ukrainian experts. On a side
note, the Workshop was warmly welcomed by the
Black Sea Fleet Command. In the years to come a to-
tal of 11 Workshops would be held all across Russia
from Chernogolovka (1975) near Moscow to Kungur
(1991) in the Urals. The most memorable were the
“floating” Workshops that used a motor ship as a
venue and traveled from Krasnoyarsk to Dudindka
(Siberia) in 1975 and from Perm to Volgograd (east
61
In Cyrillic, ЕС.
FIRST DECADES IN THE SOVIET UNION S467
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
of European Russia) in 1979. The Workshops covered
nearly all of magnetic resonance phenomena.
It would only be fitting to conclude this mono-
graph with the events of the year 1969, central to
both the USSR and the world in the context of mag-
netic resonance.
In that year, the Journal of Magnetic Resonance
and the Organic Magnetic Resonance (later, Magnetic
Resonance in Chemistry)– world’s leading journals in
the field of magnetic resonance – were established.
In the editorial board of the latter the USSR was
represented by E.  Lippmaa who, on a side note, in
the same year earned his doctoral degree in physics
and mathematics at the Institute of Chemical Physics,
USSR Academy of Sciences.
Finally, in 1969, the International Conference was
held in Kazan to mark the 25-year anniversary of
E.  K.  Zavoisky’s discovery of EPR. Despite all the faults
and pitfalls, magnetic resonance and related phenom-
ena research continued to develop in the USSR, al-
though, leading positions in the world were hardly the
case. There were rare exceptions though. Physicists
of the Novosibirsk school (Y.  N.  Molin, K.  M.  Salikhov,
R.  Z.  Sagdeev, etal.) made breakthrough developments
in the studies of chemically induced nuclear spin po-
larization in radical combination reactions, while their
colleagues at the University of Kazan (S.  A.  Altshuler,
M.  A.  Teplov et al.) delivered groundbreaking results
in exploring Van Vleck paramagnetism.
Supplementary information
The online version contains supplementary material
available at https://doi.org/10.1134/S0006297925604502.
Acknowledgments
We are grateful to Sergei P. Dolin, Marianna V. Vo-
evodskaya, Elena O. Vetrova, Vladimir N. Linev, Yurii
I. Talanov, Gertz I. Likhtenshtein, Anatoly F. Vanin,
Mikhail. A. Ostrovsky, Irina Yu. Pavlovskaya, Yu. N. Mo-
lin, Ilya P. Amiton, and Galina V. Lagodzinskaya for
their kind permission to reproduce the photographs.
Funding
This work was carried out within the framework of
the State Assignment for the Lomonosov Moscow State
University and State Assignment for the Emanuel In-
stitute of Biochemical Physics, Russian Academy of
Sciences (no.001201253314).
Ethics approval and consent to participate
This work does not contain any studies involving hu-
man and animal subjects.
Conflict of interest
The authors of this work declare that they have no
conflicts of interest.
REFERENCES
1. Zavoisky, E. K. (1945) Paramagnetic relaxation in liq-
uid solutions with perpendicular field [in Russian],
Soviet Phys. JETP, 15, 344-350.
2. Zavoisky, E. K. (1945) Paramagnetic relaxation of liq-
uid solutions for perpendicular fields, J.Phys. USSR,
9, 211-216.
3. Zavoiskaya, N. E. (2007) A History of One Discovery
[in Russian], IDT Publishers, Moscow.
4. Silkin, I. I. (2005) Evgeny Konstantinovich Zavoisky:
AChronicle of Scientific and Pedagogical Work at the
Kazan University, KGU Publishing House, Kazan.
5. Participant list for the P.  L. Kapitsa seminar at the
IPP, 30 December, 1944 [in Russian] (1944) The Ar-
chive of the Russian Academy of Sciences, fond 1943.
6. Transcript of the meeting of the Scientific Council of
the Physical Institute of the Academy of Sciences of
the USSR, 30 January, 1945 [in Russian] (1945) The
Archive of the Russian Academy of Sciences, fond
532, inventory 1, folder 106.
7. Bulletin of the Academy of Sciences of the USSR. Phys-
ical Series (1947) 11, # 2.
8. Bulletin of the Academy of Sciences of the USSR. Phys-
ical Series (1947) 11, # 3-4.
9. Bulletin of the Academy of Sciences of the USSR. Phys-
ical Series (1947) 11, # 5-6.
10. Dorfman, Y. G. (1947) Nuclear magnetic moments in
the condensed phase [in Russian], Bull. Acad. Sci.
USSR Phys. Ser., 11, 598-606.
11. Ioffe, A. F. (1947) Thirty years of the Soviet physics
[in Russian], Bull. Russ. Acad. Sci. Phys., 11, 581-590.
12. Cummerow, R.  L., and Halliday, D. (1946) Paramag-
netic losses in two manganous salts, Phys. Rev.,
70, 433.
13. Gorter, C. J. (1947) Paramagnetic Relaxation, Elsevier,
Amsterdam.
14. Ginzburg, V.  L. (1947) Radiospectroscopy of mole-
cules, Soviet Physics Uspekhi, 31, 320-343.
15. Purcell, E. M., Torrey, H.  C., and Pound, R. V. (1946)
Resonance absorption by nuclear magnetic moments
in a solid, Phys. Rev., 69, 37-38, https://doi.org/10.1103/
PhysRev.69.37.
16. Bloch, F., Hansen, W. W., and Packard, M. (1946) Nu-
clear Induction, Phys. Rev., 69, 127, https://doi.org/
10.1103/PhysRev.69.127.
17. Aminov, L. K. (1998) Spin-lattice relaxation studies
in Kazan University, in Foundations of Modern EPR
(Eaton, G. R., Eaton S.  S., and Salikhov, K. M., eds)
World Scientific Publishing Co. Pte. Ltd., Singapore,
pp.51-56.
18. Yablokov, Yu. V. (1998). Paramagnetic resonance in
the early years at the Zavoisky Institute, in Founda-
tions of Modern EPR (Eaton, G. R., Eaton S.  S., and
Salikhov, K.  M., eds) World Scientific Publishing Co.
Pte. Ltd., Singapore, pp.57-62.
KESSENIKH, PTUSHENKOS468
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
19. Altshuler, N.  S., and Larionov A. K. (2014) Pages in the
life of Altshuler S. A., scientific and personal in Re-
garding the Study of The Phenomenon of Soviet Phys-
ics in 1950-1960s. Sociocultural and Interdisciplinary
Aspects. (Vizgin, V. P., Kessenikh, A. V., and Tomilin,
K. A., eds) [in Russian], RHGA, St.  Petersburg, pp.263-
314.
20. (1960) Paramagnetic Resonance: Proceedings of the
Meeting on Paramagnetic Resonance (Kazan, 2-5
June, 1959) (Altshuler, S. A., and Kozyrev, B. M., eds)
[in Russian], KGU Publishing House, Kazan.
21. Manenkov, A.  A., and Prokhorov, A. M. (1955) The
fine structure of the spectrum of the paramagnetic
resonance of the ion Cr
3+
in chromium corundum,
Soviet Physics JETP, 1, 611.
22. Zhabotinsky, M.  E. (1955) Radio spectroscopy and mo-
lecular structure [in Russian], Russ. Chem. Rev., 24,
730-758.
23. (1945) Research Plan of the Academy of Sciences of
the USSR for the Year 1946 [in Russian], The USSR
Academy of Sciences Publishing House, Moscow-Len-
ingrad, pp.41-42.
24. Blumenfeld, L.A. (1992) Personal reminiscences,
in The Institute of Chemical Physics (Essays on the
History) (Dubovitskii, F. I., ed.) 2nd ed. Nauka, Cher-
nogolovka, pp.509-514.
25. Syrkin, Ya.  K (1939) The use of physical methods in
organic chemistry [in Russian], in: Proceedings of the
Session of Academy of Sciences on Organic Chemis-
try, Academy of Sciences of USSR, Moscow-Leningrad,
pp.261-281.
26. Wolkenstein,M., and Syrkin, J. K. (1937) Raman spec-
tra of oxonium compounds, Nature, 139, 288-289,
https://doi.org/10.1038/139288b0.
27. Wassiliew, W., Syrkin, J., and Kenez, I. (1935) Dipole
moment of iodine, Nature, 135, 71, https://doi.org/
10.1038/135071c0.
28. Waters, W. A. (1946) The Chemistry of Free Radi-
cals, Clarendon Press, Oxford, https://doi.org/10.1002/
pol.1947.120020314.
29. Blumenfeld, L. A. (1957) Paramagnetic resonance
spectra of biological objects and migration energy [in
Russian], Izv. Akad. Nauk SSSR, Ser. Biol., 3, 285.
30. Blumenfeld, L. A., and Kalmanson, A.  E. (1957) The
EPR spectra of biological objects. 1. Effects of ionizing
radiation on the dry specimens of amino acids, pep-
tides, proteins, and lyophilized tissues [in Russian],
Russ.J. Biophys. (Biofizika), 2, 552-565.
31. Terenin, A.  N., and Krasnovsky, A. A. (1949) The prob-
lem of energy migration in biological processes [in
Russian], Physics Uspekhi, 37, 65-73.
32. Molin, Y. N., Koritsky, A.  T., Buben, N. Y., and Vo-
evodsky, V.  V. (1958) Investigations of free radicals
produced in solids under fast-electron bombard-
ment [in Russian], Dokl. Akad. Nauk SSSR, 123,
882-883.
33. Chernyak, N. Y., Bubnov, N. N., Voevodsky, V. V., Polak,
L. S., and Tsvetkov, Y. D. (1958) Formation of free rad-
icals and atoms in hydrocarbon radiolysis at 77°K [in
Russian], Dokl. Akad. Nauk SSSR, 120, 346-348.
34. Tsvetkov, Y. D., Voevodsky, V. V., Razuvaev, G. A.,
Sorokin, Y. V., and Domrachev, G.  A. (1957) Electron
paramagnetic resonance in some chromium-contain-
ing aromatic compounds of sandwich structure [in
Russian], Dokl. Akad. Nauk SSSR, 115, 118-121.
35. Panfilov, V.  N., Tsvetkov, Y. D., and Voevodsky, V. V.
(1960) EPR detection of hydrogen atoms in hydrogen
low-pressure flames [in Russian], Kinet. Catal., 1, 333.
36. Vladimirskii, K. V. (1947) On oscillatory phenomenon
in nuclear paramagnetism [in Russian], Dokl. Akad.
Nauk SSSR, 58, 1625-1628.
37. Khutsishvili, G. R. (1950) Fine structure of nuclear
magnetic resonance absorption [in Russian], Physics
Uspekhi, 42, 324-327.
38. Gvozdover, S. D., and Magazanik, A. A. (1950) Magne-
to-spin resonance studies of atomic nuclear paramag-
netism [in Russian], J.  Exp. Theor. Phys., 20, 701-705.
39. Kondorsky, E. I., and Smolkov, N. A. (1953) Ferromag-
netic resonance in nickel-zinc ferrites [in Russian],
Dokl. Akad. Nauk SSSR, 93, 237-240.
40. Kessenikh, A. V., and Markolia, A. A. (2018) Nuclear
magnetic resonance method at Sukhumi Physical
Technical Institute (1949-1959) [in Russian], Stud.
History Sci. Technol., 39, 27-37.
41. Turov, E.  A., and Vonsovsky, S. V. (1953) Concerning
the line width of ferromagnetic resonance absorption
[in Russian], J. Exp. Theor. Phys., 24, 501-502.
42. Kastler, A. (1971) On the prehistory of electron para-
magnetic resonance discovery, in Paramagnetic Reso-
nance (1944-1969) [in Russian], Nauka, Moscow, p.14.
43. Altshuler, S. A. (1952) Resonant absorption of sound
in paramagnetic media [in Russian], Dokl. Akad.
Nauk. SSSR, 85, 1253-1238.
44. Altshuler, S. A. (1955) On the theory of electron and
nuclear paramagnetic resonance under the action of
ultrasound, Soviet Physics JETP, 1, 37-44.
45. Koloskova, N. G., and Kopvillem, U. H. (1960) The line
shape of the nuclear acoustic resonance, Soviet Phys-
ics JETP, 11, 973-974.
46. Golenishchev-Kutuzov, V.  A. (1963) Nonresonant para-
magnetic absorption of sound in chrome alum, Soviet
Phys. JETP, 17, 44-45.
47. Golenischev-Kutuzov, V.  A., Kopvillem, U. H., and Nag-
ibarov, V.  R. (1968) Ultrasound generation by means
of the nuclear spin system [in Russian], JETP Lett.,
8, 445.
48. Kochelaev, B. I. (1963) Antiferromagnetism due to
spin-phonon interaction, Soviet Phys. JETP, 17, 161-
163.
49. Kochelaev, B. I. (1960) Contribution to the theory of
spin-lattice relaxation of nuclear spins in ionic crys-
tals, Soviet Phys. JETP, 37, 171-175.
FIRST DECADES IN THE SOVIET UNION S469
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
50. Aminov, L. K. (1962) On the theory of spin-lattice re-
laxation in paramagnetic ionic crystals, Soviet Phys.
JETP, 15, 547-549.
51. Aminov, L. K., and Kochelaev, B. I. (1962) Spin-spin in-
teraction via a phonon field in paramagnetic crystals,
Soviet Physics JETP, 15, 903-905.
52. Garifyanov, N. S., Kamenev, S. E., and Ovchinnikov,
I. V. (1970) EPR study of dithiophosphate, dithiocar-
bamate, and xanthate complexes of Cr(V), Mo(V),
and W(V), Theor. Exp. Chem., 3, 401-408, https://
doi.org/10.1007/BF00524661.
53. Kozyrev, B. M., and Ovchinnikov, I.  V. (1978) EPR stud-
ies of coordination compounds in liquid crystals, in
Problems of Magnetic Resonance (Prokhorov, A.  M.,
chief ed.) [in Russian], Nauka, Moscow, pp.49-65.
54. Galyametdinov, Y.  G., Ovchinnikov, I. V., Bolotin,
B. M., Étingen, N.  B., Ivanova, G. I., and Yagfarova,
L. M. (1984) Liquid crystal complexes of copper
with Schiff bases, Russ Chem Bull, 33, 2174-2176,
https://doi.org/10.1007/BF00954110.
55. Ovchinnikov, I. V., Bikchantaev, I. G., and Galyamet-
dinov, Y.  G. (1990) Paramagnetic liquid crystalline
metal complexes, in Radio-Frequency Spectroscopy
of Condensed Media [in Russian], Nauka, Moscow,
pp.61-90.
56. Ovchinnikov, I. V., and Galyametdinov, Y. G. (2001)
Magnetic liquid crystals based on coordination
compounds [in Russian], Mendeleev Chem. J., 155,
74-79.
57. Yablokov, Y. V., and Ablov, A. V. (1962) Electron para-
magnetic resonance in anhydrous cupric salts of mo-
no-carboxylic acids [in Russian], Dokl. Akad. Nauk
SSSR, 144, 173-176.
58. Ryzhmanov, Y.  M., Yablokov, Y. V., Kozyrev, B. M., Mat-
evosyan, R. O., and Stashkov, L. I. (1965) Investigation
of the electron-spin resonance in the biradicals of the
hydrazine series [in Russian], Dokl. Akad. Nauk SSSR,
164, 1073-1076.
59. Yablokov, Y. V., Voronkova, V. K., and Mosina, L.  V.
(1988) Paramagnetic Resonance of Exchange Clusters
[in Russian], Nauka, Moscow.
60. Garifyanov, N. S. (1957) Paramagnetic resonance in
alkali metals, Soviet Physics JETP, 5, 111-112.
61. Dyson, F. J. (1955) Electron spin resonance absorption
in metals. II. Theory of electron diffusion and the skin
effect, Phys. Rev., 98, 349-359, https://doi.org/10.1103/
PhysRev.98.349.
62. Zamaleev, I.  G., Kessel, A. R., Teitelbaum, G.  B., and
Kharakhashyan, E. G. (1972) Conduction electron
spin-resonance line shape of metal films [in Russian],
Phys. Metals Metallogr., 34, 16-20.
63. Berim, G. O., Cherkasov, F.  G., Kharakhashyan, E. G.,
and Talanov, Y. I. (1977) Line shape of conduction
electron spin resonance in spherical metal par-
ticles, Phys. Status Solidi A, 40, K53-K55, https://
doi.org/10.1002/pssa.2210400156.
64. Garifyanov, N.  S., and Starikov, M. A. (1959) Electron-
ic paramagnetic resonance in alloys of alkali metal,
Soviet Physics JETP, 35, 553-554.
65. Zamaleev, I. G., and Kharakhashyan, E. G. (1978) Spin
relaxation of conduction electrons at an arbitrary
probability of scattering from the surface of a metal,
JETP Lett., 27, 641-644.
66. Cherkasov, F. G., Kharakhash’yan, E. G., Medvedev,
L. I., Novosjelov, N. I., and Talanov, Y. I. (1977) Obser-
vation of intrinsic spin-lattice relaxation of conduc-
tion electrons in metallic lithium, Phys. Lett. A, 63,
339-341, https://doi.org/10.1016/0375-9601(77)90923-9.
67. Kharakhashyan, E. G., Cherkasov, F.  G., Vitol, Y. A.,
Kessel, A. R., and Yudanov, V.  F. (1972) Observation
of conduction-electron spin echo in lithium metal [in
Russian], JETP Lett., 15, 156-159.
68. Talanov, Y. I., Cherkasov, F. G., Chernov, S. F., and
Kharakhashyan, E. G. (1986) Direct observation of the
freezing-in of the spin-lattice relaxation of the elec-
trons in small metallic particles [in Russian], J. Exp.
Theor. Phys., 43, 337-338.
69. Zhikharev, V. A., Staroverov, A. P., Talanov, Y. I.,
Cherkasov, F.  G., and Chernov, S. F. (1987) Spin echo
study of electron spin-lattice relaxation in small sil-
ver particles [in Russian], Physics Solid State, 29,
1706-1712.
70. Mitrikas, G., Trapalis, C. C., and Kordas, G. (1999)
Electron spin-lattice relaxation of silver nanoparticles
embedded in SiO
2
and TiO
2
matrices, J.Chem. Phys.,
111, 8098-8104, https://doi.org/10.1063/1.480143.
71. Altshuler, T. S., Garifullin, I.  A., and Kharakhashyan,
E. G. (1972) Observation of electron spin resonance
in a type-II superconductor [in Russian], Physics Solid
State, 14, 263-264.
72. Alekseevsky, N. E., Garifullin, I.  A., Kochelaev, B. I.,
and Kharakhashyan, E. G. (1973) Electron spin reso-
nance on localized magnetic states in the super-con-
ducting system La-Er [in Russian], JEPT Lett., 18, 323-
326.
73. Rettori, C., Davidov, D., Chaikin, P., and Orbach, R.
(1973) Magnetic resonance of a localized magnet-
ic moment in the superconducting state: LaRu
2
:Gd,
Phys. Rev. Lett., 30, 437-440, https://doi.org/10.1103/
PhysRevLett.30.437.
74. Alekseevsky, N. E., Garifullin, I.  A., Garifyanov, N.  N.,
Kochelaev, B. I., Nizhankovsky, V.  I., Tagirov, L. R.,
and Khlybov, E.  P. (1988) Cu
2+
paramagnetic centers
in YBa
2
Cu
3
O
x
samples of various degrees of orthor-
hombicity [in Russian], Phys. Solid State, 30, 1568-
1570.
75. Talanov,Y., Salakhutdinov,L., Adachi,T., Noji,T., and
Koike,Y. (2015) EPR study of the local magnetic field
distribution over the Bi
2
Sr
2
Ca
1–x
Y
x
Cu
2
O
8+y
crystal
surface above the superconducting transition tem-
perature, Appl. Magn. Reson., 46, 897-907, https://
doi.org/10.1007/s00723-015-0685-0.
KESSENIKH, PTUSHENKOS470
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
76. Garifullin, I. A., Goryunov, Y.  V., and Khaliullin, G.  G.
(1993) Study of spin-wave resonance in a supercon-
ductor with paramagnetic impurities, Soviet Physics
JETP, 77, 81-91.
77. Khasanov, R. I., Talanov, Yu. I., Vashakidze, Yu. M., and
Teitel’baum, G.  B. (1995) Critical state of YBa
2
Cu
3
O
x
strip in perpendicular magnetic field as revealed
by the scanning ESR-probe, Physica C: Supercon-
ductivity, 242, 333-341, https://doi.org/10.1016/0921-
4534(94)02421-9.
78. Kozyrev, B.  M., and Salikhov, S.  G. (1947) Paramag-
netic relaxation in pentaphenyldicyclopentadienyl [in
Russian], Dokl. Akad. Nauk SSSR, 58, 1023-1025.
79. Garifyanov, N. S., and Kozyrev, B. M. (1958) The ox-
ygen effect on paramagnetic resonant absorption in
α-diphenyl-β-picrylhydrazyl [in Russian], Dokl. Akad.
Nauk SSSR, 118, 738-739.
80. Ikrina, M. A., Ilyasov, A. V., Kozyrev, B. M., Matevo-
syan, R. O., Ryzhmanov, Y. M., and Yablokov, Y.  V.
(1962) Hyperfine structure of electron spin resonance
spectra of α, α-diphenyl-β-triphenylmethyl hydrazyl
and its derivatives [in Russian], Dokl. Akad. Nauk
SSSR, 147, 618-621.
81. Kozyrev, B. M., Yablokov, Y. V., Matevosyan, R.  O.,
Ikrina, M. A., Ilyasov, A. V., Ryzhmanov, Y. M., Stashkov,
L. I., and Shatrukov, L.  F. (1963) Electron paramagnet-
ic resonance studies of substituted diphenylpicrylhy-
drazyl [in Russian], Opt. Spectrosc., 15, 625-635.
82. Vozdvizhensky, G. S., Gudin, N. V., Shapnik, M. S.,
Garifyanov, N.  S., and Ilyasov, A.  V. (1964) EPR studies
of electrode processes in water solutions of copper
complexes with organic amino derivatives [in Rus-
sian], Russ.J. Phys. Chem., 38, 1682-1685.
83. Vozdvizhensky, G. S., Shapnik, M.  S., Ilyasov, A. V.,
and Garifyanov, N.  S. (1965) EPR studies of electrode
processes in water solutions of copper complexes [in
Russian], Russ. J. Phys. Chem., 39, 64.
84. Ilyasov, A. V., Kargin, Y. M., Levin, Y. A., Morozova,
I. D., Sotnikova, N. N., Ivanova, V. H., and Safin, R.  T.
(1968) Electrochemically generated free radicals.
Message 1. Regeneration of carboxylic acid deriva-
tives [in Russian], Bull. Acad. Sci. USSR Chem. Sci., 4,
736-739.
85. Zverev, G. M., and Prokhorov, A. M. (1960) Electron
paramagnetic resonance spectrum of V
3+
in corun-
dum, Soviet Phys. JETP, 11, 330-333.
86. Zverev, G. M., and Prokhorov, A. M. (1961) Electron
paramagnetic resonance and spin-lattice relaxation
of Co
2+
in corundum, Soviet Phys. JETP, 12, 41-45.
87. Emelyanova, E. N., Karlov, N. V., Manenkov, A. A.,
Milyaev, V.  A., Prokhorov, A.  M., Smirnov, S. P., and
Shirkov, A. V. (1963) EPR spectrum and spin-lattice
relaxation of Cr
3+
and Fe
3+
in single crystal zinc tung-
state, Soviet Physics JETP, 17, 591-592.
88. Zverev, G.  M., Karlov, N. V., Kornienko, L. S.,
Manenkov, A. A., and Prokhorov, A. M. (1962) Appli-
cation of paramagnetic crystals in quantum electron-
ics, Soviet Physics Uspekhi, 5, 401-429.
89. Atsarkin, V. A., Mefed, A.  E., and Rodak, M. I. (1968)
Connection of electron spin-spin interactions with po-
larization and nuclear spin relaxation in ruby, Soviet
Physics JETP, 28, 877-885.
90. Mefed, A. E., and Rodak, M. I. (1971) Experimental in-
vestigation of manifestations of the nuclear spin-spin
reservoir in NMR, Soviet Physics JETP, 32, 220-225.
91. Zhabotinsky, M.  E., Mefed, A. E., and Rodak, M. I.
(1972) Common nuclear spin-spin reservoir in crys-
tals with several types of nuclear spin, Soviet Physics
JETP, 34, 1020-1025.
92. Neiman, M. B., Rozantzev, E. G., and Mamedova,
Yu. G.  (1962) Free radical reactions involving no
unpaired electrons, Nature, 196, 472-474, https://
doi.org/10.1038/196472a0.
93. Likhtenshtein, G.  I. (1968) Determination of the to-
pography of protein groups using specific paramag-
netic labels [in Russian], Mol. Biol., 2, 234-240.
94. Buchachenko, A. L., Kessenikh, A. V., and Rykov, S. V.
(1970) Dynamic polarization of nuclear spins during
chemical reactions, Soviet Physics JETP, 31, 410-415.
95. Buchachenko, A.  L. (1976) Magnetic effects in chemi-
cal reactions, Russ. Chem. Rev., 45, 375-390.
96. Salikhov, K.  M., Molin, Y.  N., Sagdeev, R.  Z., and
Buchachenko, A. L. (1984) Spin Polarization and Mag-
netic Effects in Radical Reactions, Elsevier, Amster-
dam, Oxford.
97. Likhtenshtein, G. I. (2016) Spin labeling methods,
in Electron Spin Interactions in Chemistry and Bi-
ology, Springer Cham, pp. 289-325, https://doi.org/
10.1007/978-3-319-33927-6.
98. Kazansky, V. B., Pariisky, G. B., and Voevodsky, V. V.
(1961) Radiation-induced processes on the silica-gel
surface, Discuss. Faraday Soc., 31, 203-208.
99. Kazansky, V. B., Ezhkova, Z. I., Lyubarsky, A. G.,
Voevodsky, V. V., and Ioffe, I.  I. (1961) ERP studies of
the structure of molybdenum-vanadium oxide cata-
lysts [in Russian], Kinet. Catal., 2, 862-866.
100. Kazansky, V. B., Nikitina, O. V., Pariisky, G. B., and
Kiselev, V.  F. (1963) EPR studies of molecular oxygen
radical adsorption on reduced titanium dioxide [in
Russian], Dokl. Akad. Nauk SSSR, 151, 369-372.
101. Maschenko, A. I., Sharapov, V.  M., Kazansky, V. B., and
Kiselev, B.  F. (1965) The origin of the EPR signal at
low-temperature adsorption of gases on reduced ru-
tile TiO
2
[in Russian], Theor. Exp. Chem., 1, 381-386.
102. Tsvetkov, Y. D., Lebedev, Y. S., and Voevodsky, V. V.
(1959) Studies of free radical reactions in irradiat-
ed polytetrafluorethylene [in Russian]. II. Applica-
tion of the electron paramagnetic resonance method
to the study of radical transformations and deter-
mination of the diffusion coefficient of oxygen in
polytetrafluorethylene [in Russian], Polymer Sci., 1,
1519-1525.
FIRST DECADES IN THE SOVIET UNION S471
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
103. Lebedev, Y. S., Tsvetkov, Y. D., and Voevodsky, V. V.
(1963) Studies of free radical reactions in irradiated
polytetrafluoroethylene. V. Discussion of the reactions
mechanism [in Russian], Polymer Sci., 5, 1608-1614.
104. Lebedev, Y. S., Chernikova, D. M., and Tikhomirova,
N. N. (contr.) (1962) Atlas of the electron paramagnet-
ic resonance spectra. Issue 1: Theoretically calculat-
ed multicomponent symmetric spectra (Lebedev, Y.  S.,
and Voevodsky, V. V., eds.) [in Russian], The USSR
Academy of Sciences Publishing House, Moscow.
105. Lebedev, Y. S., and Tikhomirova, N.  N. (contr.) (1964)
Atlas of the electron paramagnetic resonance spectra.
Issue 2: Theoretically calculated spectra of complex
hyperfine structures (Lebedev, Y. S., and Voevodsky,
V. V., eds.) [in Russian], Nauka, Moscow.
106. Grinberg, O. Ya., Dubinskii, A. A., and Lebedev, Ya.  S.
(1983) Electron paramagnetic resonance of free
radicals in the two-millimetre wavelength range,
Russ. Chem. Rev., 52, 850-865, https://doi.org/10.1070/
RC1983v052n09ABEH002893.
107. Lebedev, Y. S. (1994) Very-high-field EPR and its ap-
plications, Appl. Magn. Reson., 7, 339-362, https://
doi.org/10.1007/BF03162619.
108. Galkin, A. A., Grinberg, O. Y., Dubinsky, A.  A., Kabdin,
N. N., Krylov, V. N., Kurochkin, V. I., Lebedev, A. S.,
Oransky, L. G., and Shuvalov, V. F. (1977) Two-milli-
meter EPR spectropmeter for chemical research [in
Russian], Instrum. Exp. Tech., 4, 284.
109. Dekabrun, L. L., and Purmal, A.  P. (1957) Radical in-
dication by a nuclear resonance method [in Russian],
Dokl. Akad. Nauk SSSR, 116, 983-985.
110. Bystrov, V.  F., Dekabrun, L. L., Kilyanov, Y. N.,
Stepanyants, A. U., and Utyanskaya, E. Z. (1961) High-
resolution NMR instrumentation [in Russian], In-
strum. Exp. Tech., 1, 122-125.
111. Vetrov, O. D., and Dekabrun, L. L. (1964) Multipurpose
Pulse Sequence Generator [in Russian], Automat. Re-
mote Control, 24, 1589-1592.
112. Dekabrun, L. L., and Kilyanov, Y. N. (1975) Permanent
magnets for high-resolution nuclear magnetic reso-
nance spectroscopy [in Russian], Instrum. Exp. Tech.,
4, 186-188.
113. Tartakovsky, V.  A., Chlenov, E.  I., Lagodzinskaya, G. V.,
and Novikov, S. S. (1965) O-esters of trinitromethane
in the reaction of 1, 3-dipolar cycloaddition [in Rus-
sian], Dokl. Akad. Nauk SSSR, 161, 136-139.
114. Lagodzinskaya, G. V. (1970) Slow inversion and
PMR spectra of isoxalidine derivatives [in Russian],
J.Struct. Chem., 11, 25-31, https://doi.org/10.1007/
BF00743902.
115. Zabrodin, V. A., Solovyov, V. E., and Galperin, L. N.
(1971) Single source frequency synthesis for NMDR
spectrometers [in Russian], Instrum. Exp. Tech., 3,
128.
116. Nazarov, V. B., Zabrodin, V. A., Krainskii, I. S., and
Gal’perin, L. N. (1972) Compensators for non-uni-
formity of the magnetic field of a superconducting
solenoid, Cryogenics, 12, 470-471, https://doi.org/
10.1016/0011-2275(72)90036-7.
117. Nesmeyanov, A. N., Ustynyuk, Yu. A., Kritskaya, I. I.,
and Shchembelov, G.  A. (1968) Proton magnetic res-
onance spectra and structure of iron π-allyl com-
plexes, J.  Organomet. Chem., 14, 395-403, https://
doi.org/10.1016/S0022-328X(00)87679-2.
118. Kazakova, V.  M., and Syrkin, Y. K. (1960) Electron
paramagnetic resonance spectra of some aromatic
and aliphatic metal-ketyls in solutions [in Russian],
Dokl. Akad. Nauk SSSR, 133, 112-114.
119. Morozova, I. D., and Dyatkina, M. E. (1962) Spin den-
sity distribution in some metal ketyls [in Russian],
Dokl. Akad. Nauk SSSR, 146, 830-832.
120. Vanin, A. F., Blumenfeld, L. A., and Chetverikov, A.  G.
(1967) EPR study of non-heme iron complexes in cells
and tissues [in Russian], Biophysics, 12, 829-839.
121. Benderskii, V. A., Blumenfeld, L. A., Stunzas, P.  A., and
Sokolov, E. A. (1968) Double electron-electron reso-
nance of triplet excitons in ion-radical salts, Nature,
220, 365-367, https://doi.org/10.1038/220365a0.
122. Hyde, J. S., Chien, J.  C., and Freed, J. H. (1968) Elec-
tron-electron double resonance of free radicals in
solution, J.Chem. Phys., 48, 4211-4226, https://doi.org/
10.1063/1.1669760.
123. Blumenfeld, L. A., and Ignatéva, L. G. (1974) Con-
formational changes in myosin under ATP hydro-
lysis, Eur. J. Biochem., 47, 75-79, https://doi.org/
10.1111/j.1432-1033.1974.tb03669.x.
124. Tikhonov, A. N., Khomutov, G. B., Ruuge, E.  K., and
Blumenfeld, L. A. (1981) Electron transport control
in chloroplasts. Effects of photosynthetic control
monitored by the intrathylakoid pH, Biochim. Bio-
phys. Acta, 637, 321-333, https://doi.org/10.1016/0005-
2728(81)90171-7.
125. Blumenfeld, L. A. (1981) Problems of Biological Phys-
ics (Springer Series in Synergetics), Springer, New
York.
126. Grishchuk, E. L., Molodtsov, M.  I., Ataullakhanov, F. I.,
and McIntosh, J. R. (2005) Force production by disas-
sembling microtubules, Nature, 438, 384-388.
127. Razumova, L. L., Kayushin, L. P., Gun, T. S., and
Pulatova, M. K. (1962) Electron paramagnetic reso-
nance studies of different myosin structures [in Rus-
sian], Dokl. Akad. Nauk SSSR, 146, 1197-1200.
128. Brzhevskaya, O. N., Kayushin, L. P., and Nedelina,
O. N. (1966) On the existence of free radicals in en-
zymatic hydrolysis of adenosine triphosphate [in Rus-
sian], Biophysics, 11, 213.
129. Rikhireva, G. T., Umrikhina, A.  V., Kayushin, L. P., and
Krasnovsky, A. A. (1966) Free-radical states formation
at mitochondrial respiration and phosphorylation [in
Russian], Biophysics, 11, 796.
130. Ostrovsky, M. A., and Kayushin, L. P. (1963) Studies
of electron paramagnetic resonance in retina under
KESSENIKH, PTUSHENKOS472
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
light action [in Russian], Dokl. Akad. Nauk SSSR, 151,
986-988.
131. Alekseev,S., Kayushin,L., Lvov,K., and Ostrovsky,M.
(1974) Formation of paramagnetic centers in rhodop-
sin extracts and in outer segments, Studia Biophys.,
43, 193-199.
132. Ostrovsky, M.  A. (1966) Reversible change of the reti-
nal pigment epithelium EPR signal under visible light
[in Russian], Transact. Moscow Soc. Naturalists, 16,
275-279.
133. Ostrovsky, M.  A. (1969) Photoreactivity of retinal pig-
ment epithelium, in Physiology of Vision in Ordinary
and Extreme Conditions [in Russian], Nauka, Lenin-
grad, pp.110-113.
134. Kiselev, A. G., Mokulskii, M.  A., and Lazurkin, Yu. S.
(1962) The anisotropy of hyperfine splitting in the
electron spin resonance spectra of irradiated orien-
tated polymers, Polymer Sci. USSR, 3, 455-467, https://
doi.org/10.1016/0032-3950(62)90407-0.
135. Alexandrov, A. A., Gavrilov, V. Y., Kiselev, A. G.,
Lazurkin, Y. S., and Mokulsky, M. A. (1961) Concern-
ing the the origins of EPR line broadening in nucleic
acids and in nucleic acid-protein complexes [in Rus-
sian], Dokl. Akad. Nauk. SSSR, 141, 1483-1485.
136. Usaty, A. F., Panin, B.  I., Ponomareva-Stepnaya, M. A.,
and Molodov, L.  A. (1968) Localization of free radicals
in irradiated alanine-glycine peptides [in Russian],
High Energy Chem., 2, 444-448.
137. Usaty, A. F., and Panin, B. I. (1973) Secondary free-rad-
ical reactions in irradiated frozen water solutions of
amino-acids and peptides [in Russian], Biophysics, 18,
439-446.
138. Skripov, F. I. (1958) A nuclear-resonance generator in
the Earth’s magnetic field [in Russian], Dokl. Akad.
Nauk SSSR, 121, 998-1000.
139. Morozov, A. A., Melnikov, A. V., and Skripov, F. I.
(1958) Method of free nuclear induction in a weak
magnetic field as applied to certain problems in high
resolution radio-frequency spectroscopy [in Russian],
Bull. Acad. Sci. USSR, 22, 1141.
140. Ustynyuk, Y. A. (2016) Lectures on Nuclear Magnetic
Resonance Spectroscopy. Part 1 (an Introductory
Course) [in Russian], Technosphera, Moscow.
141. Borodin, P. M., and Skripov, R. N. (1958) Chemical
shifts and fine structure of
19
F NMR signals. II. flu-
orine-containing compounds [in Russian], Izvestia
VUZ. Radiofizika, 1, 69-80.
142. Shutilov, V. A. (1962) Nuclear magnetic resonance
and ultrasound. Review [in Russian], Akust. Zhurn.,
8, 383-406.
143. Shutilov, V. A., and Antokolsky, G. L. (1967) Ultrasonic
agitation of magnetic dipole transitions of F
19
nuclei
in LiF single crystals [in Russian], Physics Solid State,
9, 1231-1234.
144. Shutilov, V. A., and Antokolsky, G.  L. (1969) Acous-
tic saturation of nuclear spin levels in piezoelec-
tric crystals [in Russian], Physics Solid State, 11,
1601-1603.
145. Zhitnikov, R.  A., Kolesnikov, N. V., and Kosyakov, V. I.
(1962) Paramagnetic resonance of free silver atoms
trapped in nonpolar media at 77°K [in Russian],
J. Exp. Theor. Phys., 43, 1186-1196.
146. Baranov, P.  G., Zhitnikov, R. A., and Melnikov, N. I.
(1968) Paramagnetic resonance of silver atoms stabi-
lized in alkali halide crystals, Phys. Stat. Solidib, 30,
851-858, https://doi.org/10.1002/pssb.19680300245.
147. Zhitnikov, R.  A., Kuleshov, P. P., and Okunevitch,
A. I. (1969) Mixing in the excited state of
85
Rb and
87
Rb atoms at optical pumping in inert gases, Phys.
Lett. A, 29, 239-240, https://doi.org/10.1016/0375-
9601(69)90356-9.
148. Baranov, P.G., Bundakova, A. P., Soltamova, A. A.,
Orlinskii, S. B., Borovykh, I.  V., Zondervan, R.,
Verberk,R., and Schmidt,J. (2011) Silicon vacancy in
SiC as a promising quantum system for single- defect
and single-photon spectroscopy, Phys. Rev. B, 83,
125203, https://doi.org/10.1103/PhysRevB.83.125203.
149. Baranov, P. G., von Bardeleben, H. J., Jelezko, F., and
Wrachtrup, J. (2017) Magnetic Resonance of Semicon-
ductors and Their Nanostructures, Springer Vienna,
Vienna, https://doi.org/10.1007/978-3-7091-1157-4.
150. Ptushenko, V. V., and Zavoiskaya, N. E. (2017) EPR in
the USSR: the thorny path from birth to biological
and chemical applications, Photosynth. Res., 134, 133-
147, https://doi.org/10.1007/s11120-017-0432-5.
151. Ptushenko, V.  V., and Linev, V. N. (2022) A Review of the
Dawn of Benchtop EPR Spectrometers – Innovation
That Shaped the Future of This Technology, Molecules,
27, 5996, https://doi.org/10.3390/molecules27185996.
152. Lippmaa,E. (1962) High-resolution nuclear magnetic
resonance spectrometer using spin stabilization [in
Russian], Transact. Tallinn Polytech. Institute. Ser. A
(A Collection of Papers on Chemistry and Chemical
Technology. VIII), 195, 65-78.
153. Kessenikh, A. V. (2007) Our “Lühike jalg” to Europe
in Scientific Society of USSR Physicists. 1950s-1960s
and later years. Issue2 [in Russian], RHGA, St. Peters-
burg, pp.574-578.
154. Reutov, O. A., Shatkina, T. N., Lippmaa, E.  T., and
Pekh, T.  I. (1968) A new method for
13
C NMR spec-
trometry of molecular rearrangements [in Russian],
Dokl. Akad. Nauk SSSR, 181, 1400-1402.
155. Lippmaa,E., Pehk,T., Buchachenko, A. L., and Rykov,
S. V. (1970) Chemically induced dynamic nuclear po-
larization of
13
C nuclei in the thermal decomposition
of organic peroxides, Chem. Phys. Lett., 5, 521-524,
https://doi.org/10.1016/0009-2614(70)85125-9.
156. Bonch-Bruevich, V. L., Bugai, A. A., Grachev, V. G.,
Paton, B. E., Pekar, S. I., Perlin, Y.  E., Prikhot’ko, A.  F.,
Roitsin, A. B., Snitko, O. V., and Shteinshleiger, V. B.
(1978) Mikhail Fedorovich Deigen (Obituary), Soviet
Physics Uspekhi, 21, 723-724.
FIRST DECADES IN THE SOVIET UNION S473
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
157. Deigen, M. F., and Zheru, I.  I. (1967) Electron-nuclear
double resonance of F centers in MgO [in Russian],
Physics Solid State, 9, 2611-2618.
158. Ganapolsky, E. M., and Chernets, A.  N. (1963) Ultra-
sonic agitation by means of electromagnetic surface
waves [in Russian], Dokl. Akad. Nauk SSSR, 149,
72-75.
159. Ganapolsky, E. M. (1973) Acoustic paramagnetic res-
onance of Fe
2+
and Fe
3+
in gallium arsenide [in Rus-
sian], Physics Solid State, 15, 368-375.
160. Buishvili, L. L., Khutsishvili, G. R., and Cheishvili,
O. D. (1961) Magnetic relaxation in ferromagnetic
metals, Soviet Physics JETP, 12, 507-513.
161. Buishvili, L. L., Zviadadze, M. D., and Khutsishvili,
G. R. (1968) Quantum-statistical theory of the dy-
namical polarization of nuclei in the case of non-uni-
form ESR line broadening, Soviet Phys. JETP, 28,
469-475.
162. Khutsishvili, G. R. (1958) Overhauser effect in non-
metals, Soviet Phys. JETP, 34, 1136-1137.
163. Khutsishvili, G. R. (1959) On the Overhauser effect in
nonmetals. II, Soviet Phys. JETP, 35, 720-724.
164. Sanadze, T.  I. (1958) Paramagnetic resonance in neo-
dymium nitrate, Soviet Phys. JETP, 6, 801-803.
165. Sanadze, T. I., and Khutsishvili, G.  R. (1971) Forbidden
transitions and discrete saturation in EPR lines. II,
Soviet Phys. JETP, 32, 412-416.
166. Nalbandyan, A. B., and Voevodsky, V.  V. (1949) Mech-
anism for Hydrogen Oxidation and Combustion [in
Russian], The USSR Academy of Sciences Publishing
House, Moscow-Leningrad.
167. Nalbandyan, A. B., Azatyan, V.  V., and Akopyan, L. A.
(1962) EPR detection of free atoms of hydrogen, oxy-
gen and deuterium in low-pressure hydrogen flames
and in hydrogen oxide [in Russian], Dokl. Akad. Nauk
Arm. SSR, 35, 123.
168. Sachyan, G. A., and Nalbandyan, A. B. (1964) Detec-
tion of free hydrogen and oxygen atoms in a rar-
efied flame of hydrogen sulfide with oxygen by the
method of electron paramagnetic resonance, Russ.
Chem. Bull., 13, 1250-1251, https://doi.org/10.1007/
BF00863146.
169. Garibyan, T. A., Grigoryan, G. L., Mantashyan, A. A.,
and Nalbandyan, A. B. (1967) Mechanism behind
photochemical oxidation of hydrocarbons in gaseous
phase as investigated by ESR method [in Russian],
Dokl. Akad. Nauk SSSR, 176, 866-868.
170. Garibyan, T.A., Mantashyan, A. A., and Nalbandyan,
A. B. (1969) EPR studies of slow gas-phase reactions
[in Russian], Dokl. Akad. Nauk SSSR, 186, 1114-1115.
171. Nalbandyan, A. B., and Mantashyan, A. A. (1975) El-
ementary Processes in Slow Gas-Phase Reactions [in
Russian], Izd. Akad. Nauk Arm. SSR, Erevan.
172. Gershenzon, Y.  M., Rozenshtein, V.  B., and Nalbandyan,
A. B. (1987) Magnetic Resonance in Gases [in Rus-
sian], Izd. AN Arm. SSR, Erevan, Erevan.
173. Shaposhnikov, I.  G. (1947) Concerning the thermody-
namic theory of paramagnetic absorption in weak
magnetic fields [in Russian], J. Exp. Theor. Phys., 17,
824-829.
174. Shaposhnikov, I.  G. (1948) Concerning the thermody-
namic theory of spin-spin relaxation in paramagnets
[in Russian], J. Exp. Theor. Phys., 18, 533-538.
175. Shaposhnikov, I.  G. (1949) Concerning the thermody-
namic theory of paramagnetic absorption in perpen-
dicular magnetic fields [in Russian], J. Exp. Theor.
Phys., 19, 225-230.
176. Shaposhnikov, I. G. (1956) Concerning the phenome-
non of spin relaxation times in paramagnets [in Rus-
sian], Bull. Acad. Sci. USSR Phys. Ser., 20, 1255-1257.
177. Shaposhnikov, I.  G., and Kuznetsov, A. S. (1956) Con-
cerning the generalized theory of relaxation phenom-
ena [in Russian], Bull. Acad. Sci. USSR Phys. Ser., 20,
1258-1261.
178. Tsirulnikova, L. M., and Shaposhnikov, I. G. (1964)
Concerning the phenomenological theory of complex
paramagnetic susceptibility of single crystals [in Rus-
sian], Physics Solid State, 6, 2322-2326.
179. Kadyrov, D. I., and Shaposhnikov, I. G. (1970) Magnet-
ic moment dynamics of a paramagnet [in Russian],
Phys. Metals Metallogr., 29, 58-80.
180. Grechishkin, V. S. (1958) Non-stationary phenomena
in nuclear magnetic resonance, Soviet Phys. JETP,
34(7), 625-628.
181. Kurushin, A. I. (1960) Paramagnetic absorption and
rotation of plane of polarization for certain salts in
the microwave band, Soviet Phys. JETP, 37, 209-210.
182. Semakov, B. S. (1959) On the occurrence of resonance
phenomena in paramagnetics in parallel fields [in
Russian], Dokl. Akad. Nauk SSSR, 128, 706-708.
183. Grechishkin, V.  S., and Ainbinder, N. E. (1961) Nuclear
quadrupole resonance spectrum in single crystals of
urea and sodium thiosulphate [in Russian], Physics
Solid State, 3, 1821-1826.
184. Grechishkin, V. S., and Soifer, G. B. (1962) Tempera-
ture dependence of nuclear quadrupole resonance
frequencies in certain crystals [in Russian], J.Struct.
Chem., 3, 321-322, https://doi.org/10.1007/BF01151490.
185. Guschin, S. D., Shishkin, V. A., and Derendyaev, B. G.
(1967) Apparatus for observing quadrupole spin
echos in the frequency range of 150 MHz-300 MHz
[in Russian], Instrum. Exp. Tech., 5, 195-197.
186. Zelenin, V.  P., and Subbotin, G. I. (1967) EPR spectrom-
eter RE-1301with an accumulating spectral combiner
[in Russian], Instrum. Exp. Tech., 3, 106-107.
187. Zelenin, V. P., and Kushkov, V. A (1969.) Device for re-
cording spin echo signals in Radio-Frequency Spec-
troscopy [in Russian], 6, PGU, Perm, pp.209-217.
188. Morkovina, N. P., and Teterina, I.  B. (2016) Transac-
tions of the Perm State University (1916-2015). De-
partment of Physics [in Russian], Perm, URL: https://
elis.psu.ru/node/384316.
KESSENIKH, PTUSHENKOS474
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
189. Vonsovsky, S.  V., and Shur, Y. S. (1948) Ferromagnetism
[in Russian], Gostechizdat, Moscow, Leningrad.
190. Skrotsky, G.  V., and Kurbatov, L. V. (1958) Theory of
the anisotropy of the width of ferromagnetic reso-
nance absorption line [in Russian], J. Exp. Theor.
Phys., 35, 216-220.
191. Chirkov, A.  K., and Matevosyan, R. O. (1958) Paramag-
netic resonance of new organic radicals, Soviet Phys.
JETP, 33, 811-812.
192. Skrotsky, G. V., and Kokin, A. A. (1959) Theory of nu-
clear paramagnetic resonance in liquids [in Russian],
J. Exp. Theor. Phys., 36, 481-487.
193. Kokin, A. A., and Izmestev, A. A. (1965) The effects
of adsorbed substances on magnetic resonance line
shape [in Russian], Theor. Exp. Chem., 1, 242-248.
194. Molin, Y. N., Chkheidze, I. I., Buben, N. Y., and
Voevodsky, V. V. (1961) ESR investigations of the
transfer of energy to aromatic groups in radiolysis of
certain organic compounds [in Russian], Kinet. Catal.,
2, 192-196.
195. Ermolaev, V. K., Molin, Y. N., and Buben, N. Y. (1962)
Recombination of radicals in organic solids. I. Stud-
ies with the use of the freeze-pump-thaw method [in
Russian], Kinet. Catal., 3, 58-64.
196. Tsvetkov, Yu. D., Rowlands, J. R., and Whiffen, D. H.
(1964) Electron spin resonance studies of radi-
ation damage in some aliphatic acids and salts,
J.Chem. Soc., 0, 810-820, https://doi.org/10.1039/
JR9640000810.
197. Samoilova, R. I., Andrievskii, V.  N., and Tsvetkov, Y. D.
(1969) Intermolecular energy transfer in low-tem-
perature radiolysis of dialkyl sulphides [in Russian],
High Energy Chem., 3, 285-286.
198. Panfilov, V. N., and Voevodsky, V. V. (1965) The study
of reactions caused by the interaction between hy-
drogen atoms and molecules of certain compounds
in low-pressure flames, Kinet. Catal., 4, 577-584.
199. Bubnov, N. N., Bazhin, N. M., and Voevodsky, V. V.
(1964) The photosensitized decomposition of saturat-
ed hydrocarbons and alcohols in the solid phase [in
Russian], Kinet. Catal., 5, 357.
200. Bazhin, N. M., Chibrikin, V.M., and Voevodsky, V. V.
(1964) Electron paramagnetic resonance (EPR) in-
vestigation of some conjugated double bond poly-
mers, Polymer Sci. USSR, 6, 1640-1645, https://
doi.org/10.1016/0032-3950(64)90079-6.
201. Shapovalova, L. A., Bryukhovetskaya, L. V., and
Voevodsky, V. V. (1967) Concerning the interrelation-
ship between catalytic and magnetic properties of
Cr
2
O
3
gel [in Russian], Kinet. Catal., 8, 1314-1318.
202. Lebedeva, L. I., Ermolaev, V. K., and Kerkis, Y. Y. (1966)
The effect of storing irradiated peas at a temperature
of 196°C [in Russian], Dokl. Akad. Nauk SSSR, 169,
1449-1451.
203. Voevodsky, V. V. (1967) EPR relaxation methods for
studying free radicals [in Russian], The 8th Interna-
tional Symposium on Free Radicals, Conf. Abstract,
Novosibirsk, pp.131-136.
204. Raitsimring, A. M., Tsvetkov, Y. D., Zhidomirov, G. M.,
Khmelinsky, V.  E., and Semenov, A. G. (1967) Spin
echo of free radicals in solid matrices [in Russian],
Dokl. Akad. Nauk SSSR, 172, 895-898.
205. Tsvetkov, Y. D., Raitsimring, A. M., Zhidomirov, G. M.,
Salikhov, K.  M., and Voevodsky, V. V. (1968) Study of
the distribution of radicals in irradiated organic ma-
trices by the method of electron spin echo [in Rus-
sian], High Energy Chem., 2, 529-535.
206. Tsvetkov, Yu. D., and Raitsimring, A. M. (1970) Elec-
tron spin echo technique for spatial radical distri-
bution investigation in irradiated solid substances:
influence of LET and spur effects, Radiation Effects,
3, 61-64, https://doi.org/10.1080/00337577008235617.
207. Milov, A. D., Salikhov, K. M., and Tsvetkov, Y. D. (1971)
Electron spin echo studies of magnetic relaxation in
liquids: Solutions of 2, 4, 6 tri-t-butylphenoxyl, Chem.
Phys. Lett., 8, 523-526, https://doi.org/10.1016/0009-
2614(71)80082-9.
208. Salikhov, K. M. (1967) Concening the theory of bound
states of spin waves on a one-dimensional lattice [in
Russian], Phys. Metals Metallogr., 24, 12-27.
209. Zhidomirov, G. M., and Salikhov, K. M. (1971) Modu-
lation effects in free-radical spin-echo signals, The-
or. Exp. Chem., 4, 332-334, https://doi.org/10.1007/
BF00524127.
210. Skubnevskaya, G. I., Salikhov, K.  M., Smirnova, L. M.,
and Molin, Y. N. (1970) Effect of electron spin relax-
ation on exchange broadening of EPR lines in dilute
solutions [in Russian], Kinet. Catal., 11, 888-892.
211. Salikhov, K. M., Doctorov, A. B., Molin, Yu.  N., and
Zamaraev, K. I. (1971) Exchange broadening of ESR
lines for solutions of free radicals and transition met-
al complexes, J.Magnet. Reson., 5, 189-205, https://
doi.org/10.1016/0022-2364(71)90005-9.
212. Sagdeev, R. Z., Molin, Yu.  N., Salikhov, K.  M., Leshina,
T.  V., Kamha, M.  A., and Shein, S. M. (1973) Effects
of magnetic field on chemical reactions, Organic
Magnet. Reson., 5, 603-605, https://doi.org/10.1002/
mrc.1270051212.
213. Zamaraev, K.  I., Molin, Y.  N., and Skubnevskaya, G. I.
(1966) Investigation of the conformation of nick-
el-ethylene-diamine complexes in an aqueous solu-
tion by NMR, J. Struct. Chem., 7, 740-742, https://
doi.org/10.1007/BF00743763.
214. Dzizenko, A. K., Zaev, E. E., Elyakov, G. B., Molin, Y.  N.,
and Voevodsky, V. V. (1964) NMR spectra of glucosides
from ginseng roots (Panax ginseng C.A.Mey) and of
its genins [in Russian], Dokl. Akad. Nauk SSSR, 156,
92-94.
215. Molin, Y. N., and Bekker, Z.  M. (1967) Study of the
interaction of s-RNA with Mn
2+
ions on thermal de-
naturing by the method of proton relaxation [in Rus-
sian], Biophysics, 12, 337-338.
FIRST DECADES IN THE SOVIET UNION S475
BIOCHEMISTRY (Moscow) Vol. 90 Suppl. 2 2025
216. Zaev, E.  E., Molin, Y.  N., Zhidomirov, G. M., and Vo-
evodsky, V.  V. (1967) Correlation between patterns of
spin density delocalization observed in EPR studies of
radicals and in NMR studies of molecules and para-
magnetic ion complexes [in Russian], Dokl. Akad.
Nauk SSSR, 173, 1370-1373.
217. Volodarsky, L. B., Kutikova, G. A., Sagdeev, R. Z., and
Molin, Yu. N. (1968) A route to stable nitroxide radi-
cals of imidazoline N-oxide, Tetrahedron Lett., 9, 1065-
1068, https://doi.org/10.1016/S0040-4039(01)98892-6.
218. Sagdeev, R. Z., Molin, Y.  N., and Rozantsev, E. G. (1972)
NMR spectra of iminoxyl radicals [in Russian], The-
or. Exp. Chem., 5, 152-155, https://doi.org/10.1007/
BF00528038.
219. Zakharov, Y. (2001) He heard the atom speaking [in
Russian], Krasnoyarsk Rabochy, URL: https://viper-
son.ru/uploads/attachment/file/15536/k1169017.txt.
220. Mikhailov, G. M., Lundin, A. G., Gabuda, S. P., and
Alexandrov, K.  S. (1961) Proton magnetic resonance
in selenourea [in Russian], Dokl. Akad. Nauk SSSR,
141, 1406-1408.
221. Belitsky, I.  A., Gabuda, S. P., and Lundin, A. G. (1967)
Proton magnetic resonance and position of hydrogen
atoms in natural edingtonite [in Russian], Dokl. Akad.
Nauk USSR, 172, 1318-1320.
222. Lundin, A. G., Mikhailov, G. M., and Gabuda, S.  P.
(1961) The behaviour of the crystallization water in
the Rochelle salt dielectric K
4
Fe(CN)
6
∙3H
2
O [in Rus-
sian], Dokl. Akad. Nauk SSSR, 136, 864-867.
223. Lundin, A. G., Gabuda, S.  P., and Zeer, E.  P. (1969) Mi-
croscopic mechanism of spontaneous polarization in
ferroelectrics of the potassium ferrocyanide family
[in Russian], JETP Lett., 9, 432-435.
224. Moskvich, Y. N., Sukhovsky, A. A., Sorokin, A. V., and
Lundin, A. G. (1980) High-resolution
77
Se NMR studies
of ferroelectric phase transition in triglycine selenate
[in Russian], Physics Solid State, 22, 232-235.
225. Zobov, V. E., Moskvich, Y. N., Sukhovsky, A.  A., and
Dotsenko, G. I. (1976) Molecular motion effects on
the decay of multiple spin echos in solids in Radio-
Frequency Spectroscopy in Solids [in Russian], the
Kirensky Institute of Physics, Siberian Branch of the
Academy of Science of the USSR, 2, Krasnoyarsk,
p.16.
226. Lundin, A.  G., Sergeev, N. A., and Falaleev, O. V. (1978)
Magnetic moment method in the NMR of solids, in
Problems of Magnetic Resonance (Prokhorov, A.  M.,
ed.) [in Russian], Nauka, Moscow, p.226.
227. Falaleev, O. V., Sergeev, N. A., and Lundin, A.  G. (1974)
Crystalline symmetry and orientation dependence of
the NMR second moment [in Russian], Crystallogr.
Rep., 19, 560-565.
228. Zeer, E.  P. (2015) Arnold Gennadievich Lundin, in
L. V. Kirensky’s students and collaborators [in Rus-
sian], web site of the Kirensky Institute of Physics,
Siberian Branch of the Russian Academy of Science,
URL: http://kirensky.ru/ru/history/team/lag.
229. Ptushenko, V.  V. (2019) Chain initiation [in Rus-
sian], Her. Russ. Acad. Sci., 89, 179-186, https://
doi.org/10.31857/S0869-5873892179-186.
230. Blumenfeld, L. A., Voevodsky, V.  V., and Semenov,
A. G. (1962) Application of Electron Paramagnetic
Resonance in Chemistry [in Russian], Akad. Nauk
SSSR, Novosibirsk.
231. Archives of the Institute for Analytical Instrumenta-
tion, Russian Academy of Sciences (1984) Special De-
sign Bureau of Analytical Instrumentation of the Re-
search & Engineering Association of the USSR Acad-
emy of Sciences, 1950-1983 [in Russian], Leningrad.
232. Likhtenshtein, G. I. (2000) Two Banks of the River,
Part 1, manuscript, p.247.
233. Fedin, E. I. (2007) The golden stamp of failure (rem-
iniscences on the Soviet NMR instrumentation de-
velopment), in Scientific Society of USSR Physicists.
1950s-1960s and later years. Issue 2 [in Russian],
RHGA, St. Petersburg, p. 366.
234. Kessenikh, A. V. (2014) Glimpses of history of NMR
radio-frequency spectroscopy in the Soviet Union
(reminiscences, documents, materials) [in Russian],
Stud. History Sci. Technol., 1, 119-141.
235. Nesmeyanov, A., Fedin, E. (1963) Eagerly awaiting
[in Russian], Literary Newspaper, 4717, (Oct 29, Tue
No. 130).
236. Ptushenko, V.  V., and Amiton, I. P. (2018) To turn the
tide in the Soviet scientific instrumentation: In me-
moriam Erlen I. Fedin (1926-2009), Struct. Chem., 29,
1225-1234, https://doi.org/10.1007/s11224-018-1121-5.
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