Laboratory of Electrochemically Active Compounds and Materials
logo nioch.ru


N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
of Siberian Branch of Russian Academy of Sciences

 

Department of physical organic chemistry


Шундрин


Head of Lab - Dr. Sci.,
Leonid A. Shundrin 
Tel.  (383) 330-94-32,
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

 

 

Resercher ares
  • Research areas:

    • Investigation of properties of electrochemically active organic compounds, the mechanisms of electrochemical transformations, and the features of electronic and spatial structure and reactivity of the paramagnetic intermediates of electrochemical reactions and electron transfer reactions.
    • Quantum chemical studies of the electronic structure and the potential energy surfaces of charged and neutral organic radical systems. Theoretical studies of the pathways of transformation of organic ion radicals. Interpretation of the data obtained in physiochemical experiments.
    • Development of novel organic materials with electrochemical properties, including polymeric materials.
    • Pilot studies in the field of electrochemical biosensing techniques.

 

STAFF

Staff

Employee Position Room Phone Phone in. email Publications
by years
1 Shundrin Leonid Anatolievich Lab's Head (Doct. Chem) 315 НТК, 122 330-94-32 3-63, 4-36 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Oleinik Ivan Ivanovich Leading Researcher (Doct. Chem) 312, 238 330-95-24 2-86, 3-74 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Schegoleva Lyudmila Nikolaevna Leading Researcher (Doct. Chem) 416 НТК, 417 НТК 330-56-90 2-06 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Beregovaya Irina Vladimirovna Senior Researcher (Cand. Phys. Math.) 416 НТК, 417 НТК 330-56-90 2-06 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Andreev Rodion Viktorovich Senior Researcher (Cand. Chem.) 416 НТК, 417 НТК 330-56-90 2-06 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Irtegova Irina Gennadievna Senior Researcher (Cand. Chem.) 122, П-004 330-94-32 4-36, 4-03 This email address is being protected from spambots. You need JavaScript enabled to view it.
7 Oleinik Irina Vladimirovna Senior Researcher (Cand. Chem.) 312 330-95-24 2-86 This email address is being protected from spambots. You need JavaScript enabled to view it.
8 Shundrina Inna Kazimirovna Senior Researcher (Cand. Chem.) 105, П-004 330-78-64 3-46, 4-03 This email address is being protected from spambots. You need JavaScript enabled to view it.
9 Odintsov Danila Sergeevich Researcher (Cand. Chem.) 105, 122, П-004 330-78-64 3-46,4-36,4-03 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. V. Shelkovnikov, E. Vasiliev, D. Derevyanko, A. Bukhtoyarova, V. Berezhnaya, I. Shundrina
    The holographic properties of photopolymers on the base of oxygen- and sulfur-containing spirocyclic monomers
    Journal of Materials Science, 2023,, V. 58, N 2, ,Pp. 983-995 doi:10.1007/s10853-022-08105-8, IF=4.682

2022
  1. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  2. ELECTRO-ACTIVE COPOLYMER OF METHYL METHACRYLATE AND 2((4-ACRYLOYLPIPERAZIN-1-YL)METHYL)-9H-THIOXANTHEN-9-ONE FOR MEMRISTOR MEMORY TECHNOLOGIES: ELECTROCHEMICAL AND ELECTROCHROMIC / Shundrina I.K., Bukhtoyarova A.D., Os'kina I.A., Odintsov D.S., Shundrin L.A.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 668-675. doi:10.15372/CSD2022430
  3. HEAT-RESISTANT POLYIMIDES WITH ELECTRON-ACCEPTOR PENDANT GROUPS OF THE THIOXANTHENONE SERIES FOR RESISTIVE STORAGE DEVICES WITH A LOW SWITCHING VOLTAGE/ D. S. Odintsov, I. K. Shundrina, A. A. Gismatulin, I. A. Azarov, R. V. Andreev, V. A. Gritsenko & L. A. Shundrin// Journal of Structural Chemistry, 2022, V.63, N 11, pp 811-1819 doi:10.1134/S0022476622110117, IF=1.3
  4. Hu. Han, V.N. Kovtonyuk, Yu.V. Gatilov, R.V. Andreev
    Directed synthesis of isomeric polyfluorinated dinitrotetraoxacalixarenes and bicyclooxacalixarenes
    Journal of Fluorine Chemistry, 2022, V.261-262, 110022 doi:10.1016/j.jfluchem.2022.110022, IF=2.226
  5. A.D. Kuimov, Ch.S. Becker, N.A. Shumilov, I.P. Koskin, A.A. Sonina, V.Yu. Komarov, I.K. Shundrina, M.S. Kazantsev
    Synthetic approach for the control of self-doping in luminescent organic semiconductors
    Mater. Chem. Front., 2022, V. 6, N 16, Pp. 2244-2255 doi:10.1039/D2QM00345G, IF=8.683
  6. Design of postmetallocene catalytic systems of arylimine type for olefin polymerization XIX. synthesis of n-(4-allyloxy-2,3,5,6-tetrafluorophenyl)salicylaldimines and their complexes with titanium(IV) dichlorideDICHLORIDE/ Oleynik I. V., Oleynik I. I.// doi: 10.31857/S0044460X22080133, IF=0.778
  7. Mingyang Han, Ivan Oleynik, Yanping Ma, Irina Oleynik, Gregory Solan, Xiang Hao, Wen-Hua Sun
    Modulating thermostability and productivity of benzhydryl-substituted bis(imino)pyridine-iron C2H4 polymerization catalysts through ortho-CnH2n-1 (n = 5, 6, 8, 12) ring size adjustment
    European Journal of Inorganic Chemistry, 2022, V. 2022, N 21, e202200224 doi:10.1002/ejic.202200224, IF=2.551
  8. I.V. Beregovaya, L.N. Shchegoleva
    Potential energy surfaces of a stacked dimer of benzene and its radical cation: what remains and what appears
    Phys. Chem. Chem. Phys., 2022, V. 24, N 29, Pp 17547-17560 doi:10.1039/D2CP01691E, IF=3.945
  9. G.C.Krieger Filho, F.Costa, G.F.Torraga Maria, P.Bufacchi, S.Trubachev, I.Shundrina, O.Korobeinichev
    Kinetic parameters and heat of reaction for forest fuels based on genetic algorithm optimization
    Thermochimica Acta, V. 713, July 2022, 179228 doi:10.1016/j.tca.2022.179228, IF=3.378
  10. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.l. Laktionov
    Correction: Gostev et al. In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics. Polymers 2020, 12, 845
    Polymers 2022, 14(11), 2263; doi:10.3390/polym14112263, IF=4.967
  11. R.V. Andreev, I.V. Beregovaya, L.N. Shchegoleva
    Fragmentation of intermediate radical anions determines the main features of the hydrodefluorination of isomeric perfluoroxylenes. Quantum chemical substantiation
    Journal of Fluorine Chemistry, 2022, V. 257-258, 109976 doi:10.1016/j.jfluchem.2022.109976, IF=2.226
  12. 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
  13. A.Yu. Makarov, Yu.M. Volkova, S.B. Zikirin, I.G. Irtegova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.A. Nefedov, A.V. Zibarev
    New 3,1,2,4-benzothiaselenadiazines, related π-heterocycles including Herz cations, radicals and molecular complexes, and Bunte salts
    New J. Chem., 2022, ,46(7), 3687-3696 doi:10.1039/D1NJ05979C, IF=3.925
  14. 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
  15. M. Han, I.I. Oleynik, M. Liu, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    Ring size enlargement in an ortho-cycloalkyl-substituted bis(imino)pyridine-cobalt ethylene polymerization catalyst and its impact on performance and polymer properties
    Applied Organometalic Chemistry, V.36, N 2, February 2022, e6529 doi:10.1002/aoc.6529, IF=4.072
  16. G.A. Selivanova, A.D. Skolyapova, J. Wang, E.V. Karpova, I. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov
    Azo dyes containing 1,3,4-thiadiazole fragment: synthesis, properties
    New J. Chem., 2022, 46(4), 1929-1942 doi:10.1039/D1NJ05084B, IF=3.925

2021
  1. D.S. Odintsov, I.K. Shundrina, D.E. Gorbunov, N.P. Gritsan, J. Beckmann, L.A. Shundrin
    Spectroelectrochemical study of the reduction of 2-methyl-9H-thioxanthene-9-one and its S,S-dioxide and electronic absorption spectra of their molecular ions
    Phys. Chem. Chem. Phys., 2021, 23(47), 26940-26947 doi:10.1039/D1CP04464H, IF=3.676
  2. I.V. Beregovaya, I.S. Tretyakova, V.I. Borovkov
    An Updated View of Primary Ionization Processes in Polar Liquids
    The Journal of Physical Chemistry Letters, 2021, 12, 47, 11573-11577 doi:10.1021/acs.jpclett.1c03388, IF=6.475
  3. M. Han, I.I. Oleynik, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    &alpha,&alpha'-Bis (imino)-2,3:5,6-bis (pentamethylene)pyridines appended with benzhydryl and cycloalkyl substituents: Probing their effectiveness as tunable N,N,N-supports for cobalt ethylene polymerization catalysts
    Applied Organometallic Chemistry, V. 35, N 12, December 2021, e6429 doi:10.1002/aoc.6429, IF=4.105
  4. I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
    Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
    Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
  5. R.Zhang, M. Han, I.V. Oleynik, G.A. Solan, I. I. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    Boosting activity, thermostability, and lifetime of iron ethylene polymerization catalysts through gem-dimethyl substitution and incorporation of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, V.35, N 11, November 2021, e6376 doi:10.1002/aoc.6376, IF=4.105
  6. В.Н. Кручинин, Д.С. Одинцов, Л.А. Шундрин, И.К. Шундрина, С.В. Рыхлицкий, Е.В. Спесивцев, В.А. Гриценко
    Оптические и электрохромные свойства тонких пленок амбиполяных полиимидов с пендантными группами на основе производных тоиксантенона
    Оптика и спектроскопия, 2021, N 11, стр. 1393 doi:10.21883/OS.2021.11.51638.2473-21, IF=0.891
  7. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  8. Ok. Ton. Dyan, R. V. Andreev, P. A. Zaikin
    Substituents Effects in the Diels-Alder Reaction of 1,1-Difluoronaphthalen-2(1H)-ones with Cyclopentadiene
    Journal of Fluorine Chemistry, 2021, V. 250, 109859 doi:10.1016/j.jfluchem.2021.109859, IF=2.49
  9. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  10. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
    Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
    Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=3.125
  11. Influence of Comonomers on the Properties of Butylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2021, V. 63, N 5, Pp 465-470 doi:10.1134/S0965545X21050114, IF=1.206
  12. A.A. Sonina,Ch. S. Becker, A. D. Kuimov,I. K. Shundrina,V. Yu. Komarov,M.S. Kazantsev
    Alkyl-substituted bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophenes: weakening of intermolecular interactions and additive-assisted crystallization†
    CrystEngComm, 2021,V. 23, N 14, Pp 2654-2664 doi:10.1039/D0CE01794A, IF=3.545
  13. Effect of Allelic Variants of Aromatic Alcohol Dehydrogenase CADim on Micromorphological and Chemical Tissue Indices in the Spring Bread Wheat Triticum aestivum L./ A. A. Konovalov, E. V. Karpova, I. K. Shundrina, E. P. Razmakhnin, I. V. Eltsov, N. P. Goncharov// Applied Biochemistry and Microbiology, 2021, V. 57, N 4, Pp. 521-532 doi:10.1134/S0003683821040086, IF=0.886
  14. A.Yu. Vorob'ev, G.I. Borodkin, R.V. Andreev, V.G. Shubin
    1,3-Dipolar cycloaddition of cyanopyridines to heterocyclic N-imines: experimental and theoretical study
    Chemistry of Heterocyclic Compound, 2021, V.57, N 3, Pp 284-291 doi:10.1007/s10593-021-02905-7, IF=1.277
  15. H. Suo, I.V. Oleynik, I.I. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Post-functionalization of narrowly dispersed PE waxes generated using tuned N,N,N'-cobalt ethylene polymerization catalysts substituted with ortho-cycloalkyl groups
    Polymer, 2021, V. 213, 123294 doi:10.1016/j.polymer.2020.123294, IF=4.43
  16. Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062, IF=0.867

2020
  1. A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
    Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
  2. 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
  3. H. Suo, Z. Li, I.V. Oleynik, Z. Wang, I.I. Oleynik, Y. Ma, Qi. Liu, W. Sun
    Achieving strictly linear polyethylenes by the NNN-Fe precatalysts finely tuned with different sizes of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, 2020, V. 34, N 11 , e5937 doi:10.1002/aoc.5937, IF=3.14
  4. A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
    2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
    Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613
  5. B.V. Koshcheev, R.A. Bredikhin, A.M. Maksimov, V.E. Platonov, R.V. Andreev
    Reactions of 4-substituted 1-[(difluoromethyl)sulfinyl]polyfluorobenzenes with phenolate anion (20-11262MP)
    Arkivoc. - 2020. - Part VI - pp. 344-361. doi:10.24820/ark.5550190.p011.262, IF=1.053
  6. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  7. I.V. Oleynik, I.K. Shundrina, I.I. Oleyinik
    Highly active titanium(IV ) dichloride FI catalysts bearing a diallylamino group for the synthesis of disentangled UHMWPE
    Polymers for Advanced Technologies, 2020, V. 31, N 9, Pp 1921-1934 doi:10.1002/pat.4917, IF=2.578
  8. E.A. Chulanova, E.A. Radiush, I.K. Shundrina, I.Yu. Bagryanskaya, N.A. Semenov, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers
    Crystal Growth & Design, 2020, V. 20, N 9, Pp 5868-5879 doi:10.1021/acs.cgd.0c00536, IF=4.089
  9. T. V.Mezhenkova, V. V.Komarov,V. M.Karpov, I. V.Beregovaya,Ya.V.Zonov
    Synthesis of 1-(tetrafluorophenyl)perfluoro-1-phenylethanes and their cyclization into polyfluoro-9-methylfluorenes under the action of antimony pentafluoride
    Journal of Fluorine Chemistry, 2020, V. 237, 109615 doi:10.1016/j.jfluchem.2020.109615, IF=2.322
  10. L. Gurskaya, T. Rybalova, I. Beregovaya, E. Zaytseva, M. Kazantsev, E. Tretyakov
    Aromatic nucleophilic substitution: a case study of the interaction of a lithiated nitronyl nitroxide with polyfluorinated quinoline-N-oxides
    Journal of Fluorine Chemistry, 2020, V. 237, 109613 doi:10.1016/j.jfluchem.2020.109613, IF=2.322
  11. A.P. Koskin, R.V. Andreev, O.N. Primachenko, E.I. Shuvarakova, A.F. Bedilo
    Perfluorosulfonic acid polymer composites: Effect of the support and synthesis method on the acid and catalytic properties
    Molecular Catalysis, 2020, V. 492, 111006 doi:10.1016/j.mcat.2020.111006, IF=3.687
  12. 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
  13. V.А. Sannikova, I.R. Filippov, O.Yu. Karmatskikh, M.А. Panfilov, R.V. Andreev, A.Yu. Vorob’ev
    Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 8, Pp 1042-1047 doi:10.1007/s10593-020-02772-8, IF=1.519
  14. V.I. Borovkov, P.A. Potashov, I.V. Beregovaya, L.N. Shchegoleva, Yu.N. Molin
    Primary Radical Cations in Irradiated Poly(isobutylene)
    The Journal of Physical Chemistry B, 2020, V. 124, N 32 , Pp 7059-7066 doi:10.1021/acs.jpcb.0c03280, IF=2.857
  15. Synthesis of Urethane-Type Polymers with Polydimethylsiloxane Blocks for the Manufacture of Fibrous Matrices by Electrospinning/ I. K. Shundrina, I. V. Oleinik, V. I. Pastukhov, L. A. Shundrin, V. S. Chernonosova & P. P. Laktionov// Polymer Science, Series B, 2020, V. 62, N 4, Pp 385-393 doi:10.1134/S1560090420040090, IF=0.976
  16. Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328, IF=0.719
  17. R.V. Andreev, I.V. Beregovaya, L.N. Shchegoleva
    Unexpected hydrodefluorination of 3-Cl-tetrafluoropyridine. Interpretation through analysis of the potential energy surface for its radical anion
    Journal of Fluorine Chemistry, 2020, V. 234, 109513 doi:10.1016/j.jfluchem.2020.109513, IF=2.332
  18. L. A.Shundrin,I.A.Os'kina,I. G.Irtegova,A. F.Poveshchenko
    9H-Thioxanthen-9-one S,S-dioxide based redox active labels for electrochemical detection of DNA duplexes immobilized on Au electrodes
    Mendeleev Communications, 2020, V. 30, N 3, Pp 296-298 doi:10.1016/j.mencom.2020.05.011, IF=1.694
  19. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  20. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  21. D.S. Odintsov, I.K. Shundrina, I.A. Os'kina, I.V. Oleynik, J. Beckmann, L.A. Shundrin
    Ambipolar polyimides with pendant groups based on 9H-thioxanthene-9-one derivatives: synthesis, thermostability, electrochemical and electrochromic properties
    Polymer Chemistry, 2020, V. 11, N 12, Pp 2243-2251 doi:10.1039/C9PY01930H, IF=5.342
  22. J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
    Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
    Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174

2019
  1. 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
  2. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
    Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
    The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
  3. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
    Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
  4. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
  5. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
    RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
  6. V.I. Borovkov, L.N. Shchegoleva
    Magnetic Resonance Characteristics of Negative Polarons in Neat Poly(3-hexyl-thiophene)
    Journal of Physical Chemistry C, 2019, 123, 46, 28058-28065 doi:10.1021/acs.jpcc.9b08331, IF=4.309
  7. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  8. Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
    Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
    Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
  9. Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123, IF=0.541
  10. Pseudorotation of the Benzene Radical Cation Associated with HCN or CH3CN Molecules/ I. V. Beregovaya, R. V. Andreev, L. N. Shchegoleva// Journal of Structural Chemistry, 2019, V. 60, N 10, pp 1578-1583 doi:10.1134/S0022476619100020, IF=0.541
  11. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  12. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
    Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
  13. 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
  14. Effect of Aliphatic Diols and Dicarboxylic Acids on the Properties of Ethylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2019, V. 61, N 5, pp 544-554 doi:10.1134/S0965545X19050146, IF=0.984
  15. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  16. Perfluorobenzocyclobutene radical anion: A structurally flexible particle/ I.V. Beregovaya, L.N. Shchegoleva, V.I. Borovkov, V.M. Karpov// Journal of Structural Chemistry, 2019, V. 60, N 3, pp 373-376 doi:10.1134/S0022476619030041, IF=0.541
  17. Fabrication of High-Aspect-Ratio Microstructures on Tetraacrylate/Acrylamide Monomers Using Synchrotron Radiation/ D. I. Derevyanko, N. A. Orlova, V. V. Shelkovnikov, I. K. Shundrina, B. G. Goldenberg, V. P. Korolkov// High Energy Chemistry, 2019, V. 53, N 2, pp 136-142 doi:10.1134/S0018143919020048, IF=0.634
  18. 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
  19. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  20. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641

2018
  1. V.I. Borovkov, V.A. Bagryansky, G.A. Letyagin, I.V. Beregovaya, L.N. Shchegoleva, Y.N. Molin
    Manifestation of g-tensor anisotropy in the quantum beats of spin-correlated radical ion pairs
    Chemical Physics Letters, 2018, V. 712, Pages 208-213 doi:10.1016/j.cplett.2018.10.004, IF=1.685
  2. G.A. Selivanova, A.D. Skolyapova, R.I. Dralyuk, E.V. Karpova, I.K. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov, T.V. Basova, E.V. Tretyakov
    Solid-phase transitions of polymorphs of 4-(4-N,N-dialkylaminophenyl)azobiphenyl-2,3'4'-tricarbonitriles and their analogues
    Thermochimica Acta, 2018, V. 669, Pp 88-98 doi:10.1016/j.tca.2018.08.022, IF=2.188
  3. A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
    Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
    Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
  4. L.A. Shundrin, P.A. Avrorov, I.G. Irtegova, D.S. Odintsov, A.F. Poveshchenko
    Electrochemical reduction of 2,4-dimethyl(diethyl)-9-oxo-10-(4-heptoxyphenyl)-9H-thioxanthenium hexafluorophosphates and 2,4-dimethyl(diethyl)-9H-thioxanthene-9-ones
    Journal of Physical Organic Chemistry, 2018, V. 31, N 9, e3853 doi:10.1002/poc.3853, IF=1.591
  5. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  6. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  7. I.K. Shundrina, D.S. Odintsov, I.A. Os'kina, I.G. Irtegova, L.A. Shundrin
    Synthesis, electrochemical reduction and radical anions of 2-{[bis(4-amino(nitro)phenyl)]aminomethyl}-9H-thioxanthene-9-one derivatives
    European Journal of Organic Chemistry, 2018, V. 2018, N 26, Pp 3471-3480 doi:10.1002/ejoc.201800525, IF=2.882
  8. L.A. Shundrin, I.G. Irtegova, N.V. Vasilieva, V.A. Loskutov
    Electrochemical reduction, radical anions and solvation energies of 1,2,3,4-tetrafluoro-9,10-anthraquinone and its N-piperidyl derivatives in DMF and DMF-water mixtures
    Mendeleev Communications, 2018, V. 28, N 3, Pp 257-260 doi:10.1016/j.mencom.2018.05.009, IF=2.098
  9. M.S. Kazantsev, A.A. Beloborodova, A.D. Kuimov, I.P. Koskin, E.S. Frantseva, T.V. Rybalova, I.K. Shundrina, C.S. Becker, E.A. Mostovich
    Synthesis, luminescence and charge transport properties of furan/phenylene co-oligomers: The study of conjugation length effect
    Organic Electronics, , 2018, V. 56, May 2018, Pages 208-215 doi:10.1016/j.orgel.2018.01.010, IF=3.68
  10. Design of Postmetallocene Catalytic Systems of Arylimine Type for Olefin Polymerization: XVIII. Synthesis of N-Arylsalicylaldimine Ligands Containing meta-or para-Diallylamino Group and Their Titanium(IV) Complexes/ I.V. Oleynik, I.I. Oleynik// Russian Journal of Organic Chemistry, 2018, V. 54, N 4, pp 537-544 doi:10.1134/S1070428018040048, IF=0.655
  11. P.A. Fedyushin, R.Yu. Peshkov, E.V. Panteleeva, E.V. Tretyakov, I.V. Beregovaya, Yu.V. Gatilov, V.D. Shteingarts
    Purposeful regioselectivity control of the Birch reductive alkylation of biphenyl-4-carbonitrile
    Tetrahedron, 2018, V. 74, N 8, Pages 842-851 doi:10.1016/j.tet.2017.12.046, IF=2.377
  12. Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160, IF=0.658



Joomla Plugins