Department of physical organic chemistry

Head - Prof., Dr. Sci.  
Elena Grigor'evna Bagryanskaya
phone:  (383) 330-88-50, internal phone: 3-81
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

Resercher ares

• Research areas:

  • Investigation of the structure and reactivity of natural and synthetic complex organic compounds, short-lived particles, and unstable intermediates.
  • Producing new types of carbocations in the condensed phase with carborane anions, investigating their properties and interactions with various compounds.
  • Elaboration of new approaches for studying the structure and functions of proteins and nucleic acids and their complexes by nuclear magnetic resonance (NMR) and electron paramagnetic resonance (EPR).
  • Investigation of the mechanisms and parameters of the key reactions in nitroxyl-radical controlled polymerization. Studying polymer properties and structure.
  • Investigation of alkoxyamines with the controlled reactivity as a new platform for designing drugs and diagnostic tools and manufacturing modern polymeric materials.
  • Development and application of magnetic resonance methods to study reversible chemical reactions (tautomeric transformations, the isomerization processes, etc.).
  
  
   

 

STAFF

Staff

№	Employee	Position	Room	Phone	Phone in.	email	Publications
							by years
1	Bagryanskaya Elena Grigorievna	Lab's Head (Doct. Phys.Math.)	212	330-88-50	3-81	This email address is being protected from spambots. You need JavaScript enabled to view it.
2	Stoyanov Evgeny Stepanovich	Leading Researcher (Doct. Chem)	132	330-82-51	3-54	This email address is being protected from spambots. You need JavaScript enabled to view it.
3	Salnikov Георгий Efimovich	Senior Researcher	127	330-55-04	3-25	This email address is being protected from spambots. You need JavaScript enabled to view it.
4	Maryasov Alexander Georgievich	Senior Researcher (Cand. Phys. Math.)	107 НТК	330-55-95	2-68	This email address is being protected from spambots. You need JavaScript enabled to view it.
5	Parkhomenko Dmitry Aleksandrovich	Senior Researcher (Cand. Phys. Math.)	242	330-55-04	2-05	This email address is being protected from spambots. You need JavaScript enabled to view it.
6	Genaev Alexander Mikhailovich	Senior Researcher (Cand. Chem.)	102		3-91	This email address is being protected from spambots. You need JavaScript enabled to view it.
7	Rogozhnikova Olga Yurievna	Senior Researcher (Cand. Chem.)	313	330-49-81	3-34	This email address is being protected from spambots. You need JavaScript enabled to view it.
8	Tormyshev Viktor Mikhailovich	Senior Researcher (Cand. Chem.)	325	330-49-81	3-00	This email address is being protected from spambots. You need JavaScript enabled to view it.
9	Trukhin Dmitry Vladimirovich	Senior Researcher (Cand. Chem.)	223	330-49-81	4-02	This email address is being protected from spambots. You need JavaScript enabled to view it.
10	Shernyukov Andrey Vladimirovich	Senior Researcher (Cand. Chem.)	106 НТК, 102	330-55-04	3-66, 3-91	This email address is being protected from spambots. You need JavaScript enabled to view it.
11	Lomanovich Konstantin Alexandrovich	Researcher (Cand. Phys.Math.)	107 НТК	330-55-95	2-68	This email address is being protected from spambots. You need JavaScript enabled to view it.
12	Chuikov Igor Petrovich	Researcher (Cand. Chem.)	414 НТК	330-82-51	2-15	This email address is being protected from spambots. You need JavaScript enabled to view it.
13	Kaletina Polina Mikhailovna	Junior Researcher	242	330-55-04	2-05	This email address is being protected from spambots. You need JavaScript enabled to view it.
14	Ovcherenko Sergey Sergeevich	Junior Researcher	106 НТК	330-94-32	3-66	This email address is being protected from spambots. You need JavaScript enabled to view it.
15	Cherkasov Sergey Aleksandrovich	Junior Researcher	242	330-55-04	2-05	This email address is being protected from spambots. You need JavaScript enabled to view it.
16	Troitskaya Tatyana Ivanovna	Leading technologist	325	330-49-81	3-00	This email address is being protected from spambots. You need JavaScript enabled to view it.
Students
17	Spitcina Anna Sergeevna	Junior Researcher	106 НТК	330-94-32	3-66	This email address is being protected from spambots. You need JavaScript enabled to view it.
18	Nasonov Dmitry Mikhailovich	laboratory assistant	107 НТК	330-55-95	2-68	This email address is being protected from spambots. You need JavaScript enabled to view it.
PHD Students
19	Aleksandova Nadezhda Vladimirovna	Junior Researcher	127	330-55-04	3-25	This email address is being protected from spambots. You need JavaScript enabled to view it.
20	Asanbaeva Nargiz Bayuzakovna	Junior Researcher	106 НТК	330-94--32	3-66	This email address is being protected from spambots. You need JavaScript enabled to view it.

PUBLICATIONS

 

 

Laboratory staff publications (DB NIOCh)

Reviews, Articles

2023

1. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
   Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
   Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
2. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
   Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
   Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
3. K. Sato, E. Bagryanskaya, M. Affronte, S. Hill
   A Special Issue of Applied Magnetic Resonance in Honor of Professor Takeji Takui on the Occasion of his 80th Birthday
   Applied Magnetic Resonance, (2023), Published 07 January 2023 doi:10.1007/s00723-022-01520-9, IF=0.973

2022

1. N.P. Isaev, A.R. Melnikov, K.A. Lomanovich, M.V. Dugin, M.Yu. Ivanov, D.N. Polovyanenko, S.L. Veber, M.K. Bowman, E.G. Bagryanskaya
   A broadband pulse EPR spectrometer for high-throughput measurements in the X-band
   Journal of Magnetic Resonance Open, V. 14-15, June 2023, 100092 doi:10.1016/j.jmro.2022.100092
2. A.G. Maryasov, M.K. Bowman
   Anisotropic g-Tensor and Abragam’s Dipole Alphabet: New Words
   Applied Magnetic Resonance (2022), first published 23 November 2022 doi:10.1007/s00723-022-01512-9, IF=0.974
3. ACID-CATALYZED PYRIDYLIMIDAZOLINE REARRANGEMENT/ Salnikov G.E., Kirilyuk I.A., Morozov D.A., Cherkasov S.A., Genaev A.M.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 625-639. doi:10.15372/CSD2022426
4. SYNTHESIS OF SELF-HEALING POLYMERS BY RADICAL CONTROLLED POLYMERIZATION/ Cherkasov S.A., Edeleva M.V., Marque S.R.A., Bagryanskaya E.G.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 660-667. doi:10.15372/CSD2022429
5. A.V. Shernyukov, G.E. Salnikov, V.I. Krasnov, A.M. Genaev
   Cluster halogenation of adamantane and its derivatives with bromine and iodine monochloride† Check for updates
   Org. Biomol. Chem., 2022, 20(43), 8515-8527 doi:10.1039/D2OB01455F, IF=3.89
6. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
   Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
   Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
7. L. Politanskaya, Ji.Wang, N.Troshkova, I.Chuikov, I. Bagryanskayaa
   One-pot synthesis of fluorinated 2-arylchroman-4-one derivatives from 2-(triisopropylsilyl)ethynylphenols and aromatic aldehydes
   Journal of Fluorine Chemistry V. 263, November 2022, 110045 doi:10.1016/j.jfluchem.2022.110045, IF=2.226
8. A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
   DFT insights into superelectrophilic activation of α,β-unsaturated nitriles and ketones in superacids
   Org. Biomol. Chem., 2022,20(34), 6799-6808 doi:10.1039/D2OB01141G, IF=3.89
9. E.S. Stoyanov, I.V. Stoyanova
   The Chloronium Cation [(C2H3)2Cl+] and Unsaturated C4-Carbocations with C=C and C=C Bonds in Their Solid Salts and in Solutions: An H1/C13 NMR and Infrared Spectroscopic Study
   Int. J. Mol. Sci. 2022, 23(16), 9111 doi:10.3390/ijms23169111, IF=6.208
10. E.S. Stoyanov, I.Yu. Bagryanskaya, I.V. Stoyanova
    IR-Spectroscopic and X-ray-Structural Study of Vinyl-Type Carbocations in Their Carborane Salts
    ACS Omega 2022, 7, 31, 27560-27572 doi:10.1021/acsomega.2c03025, IF=4.132
11. N.A. Grigorieva, I.Yu. Fleitlikh, A.Ya. Tikhonov, V.I. Mamatyuk, E.V. Karpova, O.A. Logutenko
    Recovery of indium from sulfate solutions with D2EHPA in the presence of organic proton-donor additives
    Hydrometallurgy, Available online 11 June 2022, 105925 doi:10.1016/j.hydromet.2022.105925, IF=4.217
12. S.A. Cherkasov, P.M. Kaletina, Yu.F. Polienko, D. Parkhomenko
    The Kinetic Solvent Effect on 1,3-Dipolar Cycloaddition to 2,2,5,5-Tetramethyl-3-imidazoline-3-oxide-1-oxyl
    ChemPlusChem, V. 87, N 7, July 27, 2022, e202200119 doi:10.1002/cplu.202200119, IF=3.21
13. S. Ketter, M. Dajka, O. Rogozhnikova, S.A. Dobrynin, V.M. Tormyshev, E.G. Bagryanskaya, B. Joseph
    In situ distance measurements in a membrane transporter using maleimide functionalized orthogonal spin labels and 5-pulse electron-electron double resonance spectroscopy
    Journal of Magnetic Resonance Open (companion title to the Journal of Magnetic Resonance), Volumes 10-11, June 2022, 100041 doi:10.1016/j.jmro.2022.100041
14. Synthesis and study of azide-tetrazole tautomerism in 2-azido-6-phenylpyrimidin-4(3H)-one and 2-azido-4-chloro-6-phenylpyrimidine/ N. V. Aleksandrova, E. B. Nikolaenkova, Yu. V. Gatilov, D. N. Polovyanenko, V. I. Mamatyuk, V. P. Krivopalov// Russian Chemical Bulletin, 2022, V. 71, Pp 1266-1272 doi:10.1007/s11172-022-3529-8, IF=1.704
15. SPIN CROSSOVER AND TEMPERATURE SENSITIVITY OF PARAMAGNETIC NMR CHEMICAL SHIFTS IN AN AQUEOUS SOLUTION OF THE IRON(II) NAPHTHALENESULFONATE COMPLEX WITH TRIS(PYRAZOL-1-YL)METHANE [Fe(HC(Pz)3)2](C10H7SO3)2/ E. N. Zapolotsky, S. P. Babailov, I. P. Chuykov, V. V. Kokovkin & O. G. Shakirova// Journal of Structural Chemistry, 2022, V. 63,Pp. 923-929 doi:10.1134/S0022476622060099, IF=1.004
16. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
    Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
    Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
17. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
    Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
    Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
18. ЭПР-исследование аккумуляции и токсического влияния железа и меди в процессе развития Solanum tuberosum L. in vitro/ С. С. Хуцишвили, А. И. Перфильева, О. А. Ножкина, А. Ю. Дыркач// Журнал прикладной спектроскопии, 2022, Т. 89, № 2, Сс. 238-245. doi; 10.47612/0514-7506-2022-89-2-238-245 doi:10.1007/s10812-022-01356-y, IF=0.816
19. S.V. Dudkin, A.S. Chuprin, S.A. Belova, A.V. Vologzhanina, Yan.V. Zubavichus, P.M. Kaletina, I.K. Shundrina, E.G. Bagryanskaya, Yan.Z. Voloshin
    Hybrid iron(ii) phthalocyaninatoclathrochelates with a terminal reactive vinyl group and their organo-inorganic polymeric derivatives: synthetic approaches, X-ray structures and copolymerization with styrene
    Dalton Trans., 2022, V.,51, N 14, Pp 5645-5659 doi:10.1039/D1DT04187H, IF=4.569
20. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
    Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
    Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
21. I.O. Timofeev, L.V. Politanskaya, E.V. Tretyakov, Yu.F. Polienko, V.M. Tormyshev, E.G. Bagryanskaya, O.A. Krumkacheva, M.V. Fedin
    Fullerene-based triplet spin labels: methodology aspects for pulsed dipolar EPR spectroscopy
    Phys. Chem. Chem. Phys., 2022, V.24, N 7, Pp. 4475-4484 doi:10.1039/D1CP05545C, IF=3.945
22. L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
    Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
    European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
23. T.A. Vaganova, E. Benassi, Yu.V. Gatilov, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Polyhalogenated aminobenzonitriles vs their co-crystals with 18-crown-6: amino group position as a tool to control crystal packing and solid-state fluorescence
    CrystEngComm, 2022, V. 24, N 5, Pp 987-1001 doi:10.1039/D1CE01469B, IF=3.756
24. S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
    Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
    Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
25. Study of Cationic Porphyrins and Their Metal Complexes by ESR Techniques/ N.E. Sannikova, K.A. Zhdanova, A.S. Spitsyna, N.A. Bragina, M.V. Fedin, O.A.Krumkacheva// Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 2022, V. 48, N 1, Pp 1-8 doi:10.1134/S1070328422010031, IF=1.814
26. Antiviral Activity of Nitrosonium Cations against SARS-CoV-2 on a Syrian Hamster Model/ A. V. Shipovalov, A. F. Vanin, O. V. Pyankov, E. G. Bagryanskaya, V. D. Mikoyan, N. A. Tkachev, N. A. Asanbaeva, V. Ya. Popkova// Biophysics, 2022, V. 67, N 5, pages785-795 doi:10.1134/S0006350922050165

2021

1. S.S. Khutsishvili, T.V. Ganenko, B.G. Sukhov
   Formation and paramagnetic properties of manganese-containing bionanocomposites based on natural polysaccharide matrices
   Journal of Carbohydrate Chemistry,2021, V. 40, N 5, Pp 211-225 doi:10.1080/07328303.2021.1990314, IF=1.667
2. Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4, IF=1.222
3. Trityl radicals: synthesis, properties, and applications/ V. M. Tormyshev & E. G. Bagryanskaya// Russian Chemical Bulletin, 2021, V. 70, N 12, Pp 2278-2297 doi:10.1007/s11172-021-3345-6, IF=1.222
4. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
   Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
   Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
5. E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
   Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
   ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
6. A.A. Kuzhelev, D. Dai, V. Denysenkov, I.A. Kirilyuk, E.G. Bagryanskaya, T. F. Prisner
   Influence of Rotational Motion of Nitroxides on Overhauser Dynamic Nuclear Polarization: A Systematic Study at High Magnetic Fields
   The Journal of Physical Chemistry C, 2021, 125, 46, 25651–25659 doi:10.1021/acs.jpcc.1c06979, IF=4.125
7. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, T.V. Ganenko, K.V. Krutovsky
   Novel Nanobiocomposites Based on Natural Polysaccharides as Universal Trophic Low-Dose Micronutrients
   International Journal of Molecular Sciences, 2021, 22(21), 12006 doi:10.3390/ijms222112006, IF=5.923
8. Yu.V. Khoroshunova,D. A. Morozov,A. I. Taratayko,S. A. Dobrynin,I. V. Eltsov,T. V. Rybalova,Yu. S. Sotnikova,D. N. Polovyanenko,N. B. Asanbaeva,I. A. Kirilyuk
   The Reactions of 6-(Hydroxymethyl)-2,2-dimethyl-1-azaspiro[4.4]nonanes with Methanesulfonyl Chloride or PPh3-CBr4
   Molecules 2021, 26(19), 6000 doi:10.3390/molecules26196000, IF=4.411
9. S.S. Khutsishvili, G.P. Aleksandrova, T.I. Vaku'skaya, B.G. Sukhov
   Structural and Magnetic Properties of Biocompatible Coated Magnetite Nanoparticles for Treating Antianemi (Revised May 2021)
   IEEE Transactions on Magnetics, 2021, V. 57, N 10, 5200309 doi:10.1109/TMAG.2021.3101904, IF=1.7
10. S.A. Dobrynin, M.S. Usatov, I.F. Zhurko, D.A. Morozov, Yu.F. Polienko, Yu.I. Glazachev, D.A. Parkhomenko, M.A. Tyumentsev, Yu.V. Gatilov, E.I. Chernyak, E.G. Bagryanskaya, I.A. Kirilyuk
    A Simple Method of Synthesis of 3-Carboxy-2,2,5,5-Tetraethylpyrrolidine-1-oxyl and Preparation of Reduction-Resistant Spin Labels and Probes of Pyrrolidine Series
    Molecules 2021, 26(19), 5761 doi:10.3390/molecules26195761, IF=4.41
11. E.S. Stoyanov, I.Yu. Bagryanskaya, I.V. Stoyanova
    Isomers of the Allyl Carbocation C3H5+ in Solid Salts: Infrared Spectra and Structures
    ACS Omega, ACS Omega 2021, 6, 37, 23691–23699 doi:10.1021/acsomega.1c01316, IF=3.512
12. S.S. Ovcherenko, O.A. Chinak, A.V. Chechushkov, S.A. Dobrynin, I.A. Kirilyuk, O.A. Krumkacheva, V.A. Richter, E.G. Bagryanskaya
    Uptake of Cell-Penetrating Peptide RL2 by Human Lung Cancer Cells: Monitoring by Electron Paramagnetic Resonance and Confocal Laser Scanning Microscopy
    Molecules 2021, 26(18), 5442 doi:10.3390/molecules26185442, IF=4.41
13. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
14. A.O. Finke, M.Y. Ravaeva, V.I. Krasnov, I.V. Cheretaev, E.N. Chuyan, D.S. Baev, E.E. Shults
    Cross-Coupling-Cyclocondensation Reaction Sequence to Access a Library of Ring-C Bridged Pyrimidino-tetrahydrothebaines and Pyrimidinotetrahydrooripavines
    ChemistrySelect, 2021, V. 6,N 29, Pp 7391-7397 doi:10.1002/slct.202101790, IF=2.108
15. S.A. Cherkasov, A.D. Semikina, P.M. Kaletina, Yu.F. Polienko, D.A. Morozov, A.M. Maksimov, I.A. Kirilyuk, E.G. Bagryanskaya, D. Parkhomenko
    The Kinetics of 1,3-Dipolar Cycloaddition of Vinyl Monomers to 2,2,5,5-Tetramethyl-3-imidazoline-3-oxides
    ChemPhysChem, 2021, V.86, N 8, Pp 1080-1086 doi:10.1002/cplu.202100266, IF=2.862
16. M.K. Bowman, A.G. Maryasov
    The Direct Dimension in Pulse EPR
    Applied Magnetic Resonance, 2021, V.52, Pp 1041-1062 doi:10.1007/s00723-021-01362-x, IF=0.831
17. Reaction of Perfluorobenzocyclobutene with Isomeric Tetrafluorobenzenes in an SbF5 Medium/ T. V. Mezhenkova, V. V. Komarov, V. M. Karpov, V. R. Sinyakov, Ya. V. Zonov, V. I. Krasnov// Russian Journal of Organic Chemistry,2021, V. 57, N 8, Pp 1256-1267 doi:10.1134/S1070428021080042, IF=0.723
18. Development of the Technologies for the Synthesis of Polyfluoroaromatic Compounds, Crown Ethers, Plant Phytoimmunocorrectors and Their Introduction into the Experimental-Industrial Production/ V.V. Bardin, A. Sysoev, D.Koleno, M.M. Mitasov , E.G. Bagryanskaya// Chemistry for Sustainable Development, 2021. V.29. N3. P.240-245 doi:10.15372/CSD2021302
19. E.S. Stoyanov, I.Yu. Bagryanskaya, I.V. Stoyanova
    Unsaturated Vinyl-Type Carbocation [(CH3)2C=CH]+ in Its Carborane Salts
    ACS Omega, 2021, 6, 24, 15834–15843 doi:10.1021/acsomega.1c01297, IF=3.512
20. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry. 2021. V.32. N3. P.1261-1267 doi:10.1007/s11224-021-01732-y, IF=1.887
21. A Simple and Convenient Synthesis of a Multifunctional Spin Probe, Phosphonate Derivative of a Persistent Radical of the Triarylmethyl Series/ O. Yu. Rogozhnikova, D. V. Trukhin, N. B. Asanbaeva, V. M. Tormyshev// Russian Journal of Organic Chemistry, 2021, V. 57, Pp 905-913 doi:10.1134/S107042802106004X, IF=0.723
22. L. N. Grigor’eva,A. Ya. Tikhonov,K. A. Lomanovich,D. G. Mazhukin
    Stable Bicyclic Functionalized Nitroxides: The Synthesis of Derivatives of Aza-nortropinone–5-Methyl-3-oxo-6,8-diazabicyclo[3.2.1]-6-octene 8-oxyls
    Molecules 2021, 26(10), 3050 doi:10.3390/molecules26103050, IF=4.411
23. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
24. A.V. Shernyukov, G.E. Salnikov, D.A. Rudakov, A.M. Genaev
    The Key Role of Anionic Bromine Clusters Facilitating Br Atom Insertion into the B–H σ-Bond
    Inorganic Chemistry, 2021, 60, 5, 3106-3116 doi:10.1021/acs.inorgchem.0c03392, IF=5.165
25. Yu.F. Polienko, N.M. Kuprikova, D.A. Parkhomenko, Yu.V. Gatilov, E.I. Chernyak, I.A. Kirilyuk
    Synthesis of 2,5-Bis(spirocyclohexane)-Substituted Nitroxides: New Spin Labeling Agents
    Tetrahedron, 2021, V. 81, 131915 doi:10.1016/j.tet.2020.131915, IF=2.457
26. B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
    In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
    Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857
27. A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
    Org. Biomol. Chem., 2021, V. 19, N 4, Pp 866-872 doi:10.1039/D0OB01893G, IF=3.876
28. A. Chubarov, A. Spitsyna, O. Krumkacheva, D. Mitin, D. Suvorov, V. Tormyshev, M. Fedin, M.K. Bowman, E. Bagryanskaya
    Reversible Dimerization of Human Serum Albumin
    Molecules 2021, 26(1), 108 doi:10.3390/molecules26010108, IF=4.411

2020

1. P. Agback, A. Shernyukov, F. Dominguez, T. Agback, E.I. Frolova
   Novel NMR Assignment Strategy Reveals Structural Heterogeneity in Solution of the nsP3 HVD Domain of Venezuelan Equine Encephalitis Virus
   Molecules 2020, 25(24), 5824 doi:10.3390/molecules25245824, IF=3.266
2. L.V. Politanskaya, P.A. Fedyushin, T.V. Rybalova, A.S. Bogomyakov, N.B. Asanbaeva, E.V. Tretyakov
   Fluorinated Organic Paramagnetic Building Blocks for Cross-Coupling Reactions
   Molecules 2020, 25(22), 5427 doi:10.3390/molecules25225427, IF=3.266
3. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
   Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
   Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
4. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
   Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
   RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
5. S. Cherkasov, D. Parkhomenko, A. Genaev, G. Salnikov, M. Edeleva, D. Morozov, T. Rybalova, I. Kirilyuk, S.R-A. Marque, E. Bagryanskaya
   NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines
   Molecules 2020, 25(21), 5080 doi:10.3390/molecules25215080, IF=3.266
6. A. G. Maryasov, M. K. Bowman
   Anisotropic S=1/2 Kramers Doublets: g-Matrix, the Tensor G, and Dynamics of the Spin and Magnetic Moment
   Applied Magnetic Resonance (2020), V. 51, N 9-10, Pp 1201-1210 doi:10.1007/s00723-020-01257-3, IF=0.824
7. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
   Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
   Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
8. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
   Application of EPR to porphyrin-protein agents for photodynamic therapy
   Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
9. E.S. Stoyanov, I.V. Stoyanova
   The Mechanism of High Reactivity of Benzyl Carbocation, C6H5CH2+, during Interaction with Benzene
   ChemistrySelect, 2020, V. 5, N 29, Pp 9277-9280, This article also appears in:Organic & Supramolecular Chemistry doi:10.1002/slct.202001852, IF=1.811
10. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
11. Hybrid Photopolymer Material Based on (8-Acryloyl-1,4-dithia-8-azaspiro[4.5]decan-2-yl)methyl Acrylate and Thiol-Siloxane Component for Recording Microstructures: Synthesis and Optical and Thermomechanical Properties/ D. I. Derevyanko, V. S. Basistyi, V. V. Shelkovnikov, I. K. Shundrina, A. D. Bukhtoyarova, G. E. Sal’nikov, V. N. Berezhnaya & A. A. Chernonosov// Polymer Science, Series B, 2020, V.62, N 5, Pp 509-521 doi:10.1134/S1560090420050048, IF=0.976
12. A.G. Maryasov, M.K. Bowman
    Comment on "Modeling of motional EPR spectra using hindered Brownian rotational diffusion and the stochastic Liouville equation" [J. Chem. Phys. 152, 094103 (2020)]
    Journal of Chemical Physics, 2020, V. 153, N 2, Art.num. 027101 DOI: doi:10.1063/5.0010661, IF=2.99
13. G. Audran, E.G. Bagryanskaya, S.R. A. Marque, P. Postnikov
    New Variants of Nitroxide Mediated Polymerization
    Polymers 2020, 12(7), 1481 doi:10.3390/polym12071481, IF=3.426
14. A. M. Genaev, G. E. Salnikov, K.Yu. Koltunov
    Influence of Positive Charge on the NMR Parameters of Mono- and Diprotonated Forms of 4-Dimethylaminopyridine
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 892-897 doi:10.1007/s10593-020-02749-7, IF=1.519
15. P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
    Synthesis of Nitroxide Diradical Using a New Approach
    Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701, IF=3.267
16. N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
    Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
    Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267
17. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
18. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
19. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
20. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
21. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
    Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
    The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
22. I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
    2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
    Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267
23. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
24. Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1, IF=1.061
25. A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
    Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
    Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43

2019

1. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
   DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
   Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
2. S.V. Nikitin, J. Sanchez-Marquez, I.I. Oleynik, I. Oleynik, E.G. Bagryanskaya
   A screening DFT study of the para-substituent effect on local hyper-softness in bis(phenoxy-imine) titanium complexes to get insights about their catalytic activity in ethylene polymerization
   Molecular Catalysis, 2019, V. 469, Pp 57-67 doi:10.1016/j.mcat.2019.02.024, IF=2.938
3. A.A. Malygin, O.A. Krumkacheva, D.M. Graifer, I.O. Timofeev, A.S. Ochkasova, M.I. Meschaninova, A.G. Venyaminova, M.V. Fedin, M. Bowman, G.G. Karpova, E.G. Bagryanskaya
   Exploring the interactions of short RNAs with the human 40S ribosomal subunit near the mRNA entry site by EPR spectroscopy
   Nucleic Acids Research, 2019, V. 47, N 22, Pp 11850-11860 doi:10.1093/nar/gkz1039, IF=11.147
4. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
   Aromatic S_N^F-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
   Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
5. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
   Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
   Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
6. M.A. Bazhenov, A.V. Shernyukov, M.S. Kupryushkin, D.V. Pyshnyi
   Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
   Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 699-708 doi:10.1134/S1068162019060074, IF=0.794
7. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
   A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
   ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
8. Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075, IF=0.751
9. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
   Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
   Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
10. T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
    CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
11. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
12. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
13. Yu.V. Khoroshunova, D.A. Morozov, A.I. Taratayko, P.D. Gladkikh, Yu.I. Glazachev, I.A. Kirilyuk
    Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2036-2042 doi:10.3762/bjoc.15.200, IF=2.595
14. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
    How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
    RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
15. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
    Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
    Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
16. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
    Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
17. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
    EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
    Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
18. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
    Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
19. V.N. Kovtonyuk, Yu.V. Gatilov, G.E. Salnikov, E.V. Amosov
    Polyfluorinated tetraoxacalixarenes and bicyclooxacalixarenes. Interaction of pentafluorobenzonitrile with resorcinol, orcinol and tetrafluororesorcinol
    Journal of Fluorine Chemistry, 2019, V. 222-223, Pp 59-67 doi:10.1016/j.jfluchem.2019.04.011, IF=2.055
20. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
    Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
    J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
21. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
22. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
    Org. Biomol. Chem., 2019, V. 17, N 16, Pp 3971-3977 doi:10.1039/C9OB00640K, IF=3.49
23. Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y, IF=1.014
24. V.V. Shelkovnikov, I.Yu. Kargapolova, S.V. Korotaev, N.A. Orlova, T.V. Rybalova, I.P. Chuikov
    Three-color luminescent transformation of the julolidine pyrylo/pyridocyanine dyes in the adsorbed state
    Journal of Photochemistry and Photobiology A: Chemistry, 2019, V. 375 , Pp 181-190 doi:10.1016/j.jphotochem.2019.02.022, IF=3.261
25. V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
    Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
    Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
26. Exploration of SNF-Approach toward Functionalized Nitronyl Nitroxides/ P. Fedyushin, L. Gurskaya, E. Panteleeva, B. Koshcheev, A. Maksimov, T.V. Rybalova, E. Zaytseva, E. Tretyakov// doi:10.17677/fn20714807.2019.02.04
27. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, V.G. Shubin, H.S. Rzepa
    Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study
    Org. Biomol. Chem., 2019, V. 17, N 15, pp 3781-3789 doi:10.1039/C9OB00607A, IF=3.49
28. Zh. Zhu, G.E. Salnikov, K.Yu. Koltunov
    Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides
    Tetrahedron Letters, 2019, V. 60, N 12, Pp 857-859 doi:10.1016/j.tetlet.2019.02.026, IF=2.259
29. M. Edeleva, G. Audran, S. Marque, E. Bagryanskaya
    Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations
    Materials, 2019, V. 12, N 5, Pp. 688-707 doi:10.3390/ma12050688, IF=2.972
30. M. Edeleva, D. Morozov, D. Parkhomenko, Yu. Polienko, A. Iurchenkova, I. Kirilyuk, E. Bagryanskaya
    Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization
    Chem. Commun., 2019,V. 55, N 2, Pp 190-193 doi:10.1039/C8CC08541B, IF=6.164
31. Generation of Perfluoroand 1-Chloroperfluoroindanyl and -Benzocyclobutenyl Cations with Perfluoroalkyl Groups in the Aliphatic Ring/ T.V. Mezhenkova, V.M. Karpov, Ya.V. Zonov , I.P. Chuikov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 193–201 doi:10.1134/S1070428019020118, IF=0.751
32. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
33. D.I. Sharapa, A. Genaev, L. Cavallo, Yu. Minenkov
    A Robust and Cost-Efficient Scheme for Accurate Conformational Energies of Organic Molecules
    ChemPhysChem, 2019, V. 20, N 1, Pp 92-102 doi:10.1002/cphc.201801063, IF=3.077

2018

1. M.V. Edeleva, S.R-A. Marque, O.Yu. Rogozhnikova, V.M. Tormyshev, T.I. Troitskaya, E.G. Bagryanskaya
   Radical polymerization of radical‐labeled monomers: The triarylmethyl‐based radical monomer as an example
   Journal of Polymer Science Part A: Polymer Chemistry, 2018, V. 56, N 23, Pp 2656-2664 doi:10.1002/pola.29249, IF=2.588
2. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
   Superelectrophilic activation of 1-nitronaphthalene in the presence of aluminum chloride. Reactions with benzene and cyclohexane
   Org. Biomol. Chem., 2018, V.16, N 47, Pp 9129-9132 doi:10.1039/C8OB02653J, IF=3.423
3. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
   Oxygen-induced leakage of spin polarization in Overhauser-enhanced magnetic resonance imaging: application for oximetry in tumors
   Journal of Magnetic Resonance, 2018, V. 297, Pp 42-50 doi:10.1016/j.jmr.2018.10.005, IF=2.586
4. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
   Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
   Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
5. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
   Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
   Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
6. A.A. Kuzhelev, O.A. Krumkacheva, I.O. Timofeev, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya
   Electron-Spin Relaxation of Triarylmethyl Radicals in Glassy Trehalose
   Applied Magnetic Resonance, 2018, V. 49, N 11, pp 1171-1180 doi:10.1007/s00723-018-1023-0, IF=0.835
7. G.A. Lyubas
   Metallized nanoporous anodic alumina films and their applications
   Journal of Materials Science, 2018, V. 53, N 21, pp 15204-15212 doi:10.1007/s10853-018-2686-5, IF=2.993
8. Nitrimines: VII. Reaction of S,S′-Dimethyl-N-nitroimidodithiocarbonate with Alkali. Synthesis of S-Methyl-N-nitrothiocarbamate and Its Salts/ A. M. Astakhov, D. V. Antishin, А. А. Nefedov, G. E. Salnikov, E. S. Buka// Russian Journal of Organic Chemistry, 2018, V. 54, N 11, pp 1638-1642 doi:10.1134/S1070428018110039, IF=0.654
9. A. Kuzhelev, D. Akhmetzyanov, V. Denysenkov, G. Shevelev, O. Krumkacheva, E. Bagryanskaya, T. Prisner
   High-frequency pulsed electron-electron double resonance spectroscopy on DNA duplexes using trityl tags and shaped microwave pulses
   Phys. Chem. Chem. Phys., 2018, V. 20, N 41, Pp 26140-26144 doi:10.1039/C8CP03951H, IF=3.905
10. S.A. Dobrynin, Yu.I. Glazachev, Yu.V. Gatilov, E.I. Chernyak, G.E. Salnikov, I.A. Kirilyuk
    Synthesis of 3,4-Bis-(hydroxymethyl)-2,2,5,5-tetraethylpyrrolidin-1-oxyl via 1,3-Dipolar Cycloaddition of Azomethine Ylide to Activated Alkene
    J. Org. Chem., 2018, V. 83, N 10, Pp 5392-5397 doi:10.1021/acs.joc.8b00085, IF=4.805
11. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
12. N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
    Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
13. A.A. Kuzhelev, O.A. Krumkacheva, M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, V.M. Tormyshev, M. K Bowman, M.V. Fedin, E.G. Bagryanskaya
    Pulse EPR of Triarylmethyl Probes: New Approach for Investigation of Molecular Motions in Soft Matter
    J. Phys. Chem. B, 2018, 122 (36), pp 8624–8630 doi:10.1021/acs.jpcb.8b07714, IF=3.145
14. V.E. Romanov, I.Yu. Bagryanskaya, D.E. Gorbunov, N.P. Gritsan, E.V. Zaytseva, D. Luneau, E.V. Tretyakov
    A Crystallographic Study of a Novel Tetrazolyl-Substituted Nitronyl Nitroxide Radical
    Crystals 2018, 8(9), 334 doi:10.3390/cryst8090334, IF=2.144
15. E.V. Zaytseva, Yu.V. Gatilov, D.G. Mazhukin
    The synthesis of new functionalized 1,3,5-triazine-based stable bi- and trinitroxides of the 2,5-dihydroimidazole series
    Arkivoc, 2018, part v, 359-374 doi:10.24820/ark.5550190.p010.614, IF=1.048
16. Модификация аминогруппы полифторированных арилендиаминов в реакциях с альдегидами и хинонами/ Т.А. Ваганова, И.П. Чуйков, Е.В. Малыхин// Fluorine notes, 2018, V.119, N 4, Cc 5-6 doi:10.17677/fn20714807.2018.04.03
17. S.I. Zhivetyeva, I.A. Zayakin, I.Yu. Bagryanskaya, E.V. Zaytseva, E.G. Bargyanskaya, E.V. Tretyakov
    Interaction of a lithiated nitronyl nitroxide with polyfluorinated 1,4-naphthoquinones
    Tetrahedron, 2018, V. 74, N 28, Pp 3924-3930 doi:10.1016/j.tet.2018.05.075, IF=2.377
18. O.T. Dyan, P.A. Zaikin, D.S. Fadeev, Y.V. Gatilov, G.I. Borodkin
    1,1-Difluoronaphthalen-2(1H)-ones as building blocks for fluorinated tetraphenes
    Journal of Fluorine Chemistry,2018, V. 210, Pp 88-93 doi:10.1016/j.jfluchem.2018.03.008, IF=1.879
19. G. Audran, E. Bagryanskaya, M. Edeleva, S. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    Coordination-Initiated Nitroxide-Mediated Polymerization (CI-NMP)
    Australian Journal of Chemistry, 2018, V. 71, N 5, Pp 334-340 doi:10.1071/CH17570, IF=1.059
20. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
21. A. Vorontsov, E. Tretyakov
    Determination of Graphene Edges Energy using Hexagonal Graphene Quantum Dots and PM7 Method
    Phys. Chem. Chem. Phys., 2018, V. 20, N 21, Pp. 14740-14752 doi:10.1039/C7CP08411K, IF=3.906
22. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
23. F. Gaston, N. Dupuy, S.R-A. Marque, D. Gigmes, S. Dorey
    Monitoring of the discoloration on γ-irradiated PE and EVA films to evaluate antioxidant stability
    JJOURNAL OF APPLIED POLYMER SCIENCE, 2018, V. 135, N 18, Pp 46114-46122 doi:10.1002/app.46114, IF=1.9
24. F. Gaston, N. Dupuy, S.R-A. Marque, S. Dorey
    Evaluation of multilayer film stability by Raman spectroscopy after gamma-irradiation sterilization process
    Vibrational Spectroscopy, 2018, V.96, Pp 52-59 doi:10.1016/j.vibspec.2018.03.002, IF=1.363
25. G. Audran, E.G. Bagryanskaya, I.Yu. Bagryanskaya, M. Edeleva, P. Kaletina, S.R-A. Marque, D. Parkhomenko, E.V. Tretyakov, S.I. Zhivetyeva
    The effect of the oxophilic Tb(III) cation on Csingle bond-ON bond homolysis in alkoxyamines
    Inorganic Chemistry Communications, 2018, V. 91, Pp 5-7 doi:10.1016/j.inoche.2018.02.019, IF=1.81
26. A.A. Kuzhelev, O.A. Krumkacheva, G.Yu. Shevelev, M. Yulikov, M.V. Fedin, E.G. Bagryanskaya
    Room-temperature distance measurements using RIDME and the orthogonal spin labels trityl/nitroxide
    Phys. Chem. Chem. Phys., 2018, V. 20, N 15, Pp 10224-10230 doi:10.1039/C8CP01093E, IF=3.906
27. Synthesis and study of the azide-tetrazole tautomerism in 2-azido-4-(trifluoromethyl)-6-R-pyrimidines (R = H, 4-CLC6H4)/ Е. B. Nikolaenkova, N. V. Aleksandrova, V. I. Mamatyuk, V. P. Krivopalov// Russian Chemical Bulletin, 2018, V. 67, N 5, pp 893-901 doi:10.1007/s11172-018-2154-z, IF=0.781
28. Configurational Stability of 1,1'-Bi-2-naphthol in Superacid System HSO3F-SBF5-SO2ClF/ G. E. Salnikov, A. M. Genaev, A. V. Shernyukov, Z. Zhu, N. V. Tkachenko, K. Yu. Koltunov// Russian Journal of Organic Chemistry, 2018, V. 54, N 5, pp 792-794 doi:10.1134/S1070428018050214, IF=0.655
29. E.S. Stoyanov, I.V. Stoyanova
    Features of protonation of the simplest weakly basic molecules, SO2, CO, N2O, CO2, and others, by solid carborane superacids
    Angewandte Chemie International Edition, 2018, V. 57, N 17, Pp 4516-4520 doi:10.1002/anie.201704645, IF=12.102
30. L. Gurskaya, I. Bagryanskaya, E. Amosov, M. Kazantsev, L. Politanskaya, E. Zaytseva, E. Bagryanskaya, A. Chernonosov, E. Tretyakov
    1,3-Diaza[3]ferrocenophanes functionalized with a nitronyl nitroxide group
    Tetrahedron, 2018, V. 74, N 15, Pp 1942-1950 doi:10.1016/j.tet.2018.02.062, IF=2.377
31. Imidazoline and Imidazolidine Nitroxides as Controlling Agents in Nitroxide Mediated Polymerization/ M.V. Edeleva, S.R-A. Marque, E.G. Bagryanskaya// RUSS CHEM REV, 2018, 87(4), Pp. 328-349 doi:10.1070/RCR4765, IF=3.991
32. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
33. I.O. Timofeev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Refining Spin–Spin Distance Distributions in Complex Biological Systems Using Multi-Gaussian Monte Carlo Analysis
    Applied Magnetic Resonance, 2018, V. 49, N 3, pp 265-276 doi:10.1007/s00723-017-0965-y, IF=0.835
34. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
35. A.V. Vorontsov, S.V. Tsybulya
    Influence of Nanoparticles Size on XRD Patterns for Small Monodisperse Nanoparticles of Cu0 and TiO2 Anatase
    Ind. Eng. Chem. Res., 2018, 57 (7), pp 2526-2536 doi:10.1021/acs.iecr.7b04480, IF=3.141
36. T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, I.P. Chuikov, E.V. Malykhin
    Controlled self-assembly of π-stacked/H-bonded 1D crystal structures from polyfluorinated arylamines and 18-crown-6 (2:1).Associate vs. co-former fluorescence properties
    CrystEngComm, 2018, V. 20, N 6, Pp 807-817 doi:10.1039/C7CE01851G, IF=3.304
37. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Enhanced enantiostability of BINOL dimethyl ether under moderate acidic conditions
    Mendeleev Communications, 2018, V. 28, N 1, Pp 27-28 doi:10.1016/j.mencom.2018.01.007, IF=2.098
38. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
39. E.S. Stoyanov, I.V. Stoyanova
    Chloronium Cations in Dichloromethane Solutions as Catalysts for the Conversion of CH2Cl2 to CHCl3/CCl4 and CH3Cl/CH4
    CHEMISTRYSELECT, 2018, V.3, N 1, Pp 122-126 doi:10.1002/slct.201702738, IF=1.505
40. A.V. Vorontsov, E.N. Kabachkov, I.L. Balikhin, E.N. Kurkin, V.N. Troitskii, P.G. Smirniotis
    Correlation of Surface Area with Photocatalytic Activity of TiO2
    Journal of Advanced Oxidation Technologies, 2018, V. 21, N 1, , Art Number 20170063 doi:10.26802/jaots.2017.0063, IF=0.901
41. S. Dorey, F. Gaston, S.R-A. Marque, B. Bortolotti, N. Dupuy
    XPS analysis of PE and EVA samples irradiated at different γ-doses
    Applied Surface Science, 2018, V. 427, Pp 966-972 doi:10.1016/j.apsusc.2017.09.001, IF=4.439
42. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
43. S. Dorey, F. Gaston, N. Dupuy, M. Barbaroux, S.R-A. Marque
    Reconciliation of pH, conductivity, total organic carbon with carboxylic acids detected by ion chromatography in solution after contact with multilayer films after γ-irradiation
    European Journal of Pharmaceutical Sciences, 2018, V. 117, Pages 216-226 doi:10.1016/j.ejps.2018.02.023, IF=3.466