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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
Of the Siberian Branch of Russian Academy of Science

Ранее: В 2013 г. - образована группа органических материалов для электроники (ГРОМ) под руководством к.х.н. Евгения Алексеевича Мостовича.
В 2016 г. - группа становится подразделением лаборатории изучения нуклеофильных и ион-радикальных реакций.
В 2018 г. - группа была расформирована как самостоятельное структурное подразделение, а ее сотрудники вошли в состав лаборатории азотистых соединений.
В 2019 г. - лаборатория органической электроники становиться отдельным подразделением НИОХ под руководством к.х.н. Максима Сергеевича Казанцева.

Kazantsev M.S.

 

Head of Lab. Dr. Maxim S. Kazantsev

 

e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

 



Organic Electronics Laboroatory



The Laboratory history begins from the establishment of the research groups of organic electronic materials in 2013 headed by Dr. Evgeny A. Mostovich.

In 2016 the groups becomes a part of the laboratory of nucleophilic and radical ion reactions.

In 2018 г. the group was included in laboratory of nitrogen compounds.

In 2019 г. organic electronics lab. becomes an independent department headed by Dr. Maxim S. Kazantsev.





The main scientific tasks

:

  • Design, synthesis and the study of novel organic optoelectronics materials;
  • The study of molecular and electronics structure of materials;
  • Development of organic light-emitting semiconductors;
  • The study of organic electronics devices;
  • Electrochemical and optical properties of materials;
  • Crystallization, polymorphism, aggregation effects and the study of low-defect organic semiconductors.

 


Staff

Employee Position Room Phone Phone in. email Publications
by yearsby tipeby If
1 Kazantsev Maxim Sergeevich Senior Researcher (Cand. Chem.). Group's Head 240, 239 330-73-87 4-44 (3-68) This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Bekker Kristina Sergeevna Senior Researcher (Cand. Chem.) 239, 240 330-73-87 3-68, 4-44 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Kuzhelev Andrey Andreevich Researcher (Cand. Chem.) 242 330-55-04 2-05 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Gorodetskii Artem Aleksandrovich Junior Researcher 106 НТК 330-94-32 3-54 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Koskin Igor Pavlovich Junior Researcher 239, 240 330-73-87 3-68, 4-44 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Kuimov Anatoly Dmitrievich Junior Researcher 239, 240 330-73-87 3-68, 4-44
7 Radyush Ekaterina Alekseevna Junior Researcher 221 330-96-64 2-43 This email address is being protected from spambots. You need JavaScript enabled to view it.
8 Sonina Alina Aleksandrovna Junior Researcher 214 НТК 330-78-64 3-64 This email address is being protected from spambots. You need JavaScript enabled to view it.
9 Ten Yurii Alekseevich Junior Researcher 310 330-68-59 4-09 This email address is being protected from spambots. You need JavaScript enabled to view it.
10 Cherkasov Sergey Aleksandrovich Junior Researcher 243 330-55-04 2-05 This email address is being protected from spambots. You need JavaScript enabled to view it.
Students
11 Kiseleva Yuliya Olegovna laboratory assistant 249 This email address is being protected from spambots. You need JavaScript enabled to view it.


 

Laboratory Partners:


  • Novosibirsk State University;
  • Moscow State University;
  • University of Groningen (Netherlands);
  • Institute of Chemical Kinetics and Combustion;
  • International Tomography Center;
  • Tomsk Polytechnic University;
  • Institute of Synthetic Polymeric Materials;
  • Institute of Semiconductor Physics.

Publications over the past years

 

Публикации сотрудников подразделения (БД НИОХ СО РАН) 1 (2014 - 2020 )

Обзоры, статьи в научных журналах


    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. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
    Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
    Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
  3. 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, Advance Article doi:10.1039/C9NJ04069B, IF=3.69
  4. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  5. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  6. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  7. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  8. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  9. Д.В. Трухин, О.Ю. Рогожникова, Т.И. Троицкая, А.А. Кужелев, Е.В. Амосов, H.J. Halpern, В.В. Коваль, В.М. Тормышев
    Новые спиновые зонды: три-и гексакатионные производные стабильных радикалов трис(тетратиаарил)метильного ряда
    Журнал органической химии. 2019. Т. 55. № 3. С. 347-353. DOI:10.1134/S0514749219030030 (New Spin Probes: Triand Hexacationic Derivatives of Persistent Tris(tetrathioaryl)methyl Radicals/ D.V. Trukhin, O.Yu.Rogozhnikova, T.I. Troitskaya, A.A, Kuzhelev, E.V. Amosov,H.J. Halpernc, V.V. Koval'b, V.M. Tormyshev// Russian Journal of Organic Chemistry, 2019, V. 55, N 3, pp 296-301 doi:10.1134/S1070428019030035), IF=0.751
  10. 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=5.976

  11. 2018
  12. Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
    The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
    RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
  13. A. A. Sonina, I.P. Koskin, Pete.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
  14. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  15. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    A quantitative topological descriptor for linear co-oligomer fusion
    Chem. Commun., 2018, V. 54, N 52, Pp 7235-7238 doi:10.1039/C8CC03156H, IF=6.29
  16. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  17. 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
  18. 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
  19. 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

  20. 2017
  21. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    Way to Highly Emissive Materials: Increase of Rigidity by Introduction of a Furan Moiety in Co-Oligomers
    J. Phys. Chem. C, 2017, 121 (42), pp 23359-23369 doi:10.1021/acs.jpcc.7b08305, IF=4.535
  22. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  23. A.A. Beloborodova, V.S. Minkov, D.A. Rychkov, T.V. Rybalova, E.V. Boldyreva
    First Evidence of Polymorphism in Furosemide Solvates
    Cryst. Growth Des., 2017, 17 (5), pp 2333-2341 doi:10.1021/acs.cgd.6b01191, IF=4.54
  24. M.S. Kazantsev, A.A. Beloborodova, E.S. Frantseva, T.V. Rybalova, V.G. Konstantinov, I.K. Shundrina, D.Yu. Paraschuk, E.A. Mostovich
    Methyl substituent effect on structure, luminescence and semiconducting properties of furan/phenylene co-oligomer single crystals
    CrystEngComm, 2017,19, 1809-1815 doi:10.1039/C6CE02565J, IF=3.108
  25. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
  26. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  27. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
    Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473

  28. 2016
  29. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
    Highly-emissive solution-grown furan/phenylene co-oligomer single crystals
    RSC Adv., 2016,6(95), 92325-92329 doi:10.1039/C6RA23160H, IF=3.289
  30. L.G. Kudryashova, M.S. Kazantsev V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144

  31. 2015
  32. C. Becker, N. Chukanov, I. Grigor’ev
    New amino-bisphosphonate building blocks in the synthesis of bisphosphonic derivatives based on lead compounds
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2015, V. 190, N 7, 1201-1212. 10.1080/10426507.2014.979989 doi:10.1080/10426507.2014.979989, IF=0.561
  33. D.S. Baranov, A.G. Popov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, L.V. Kulik
    Naphtho[4,3,2,1-lmn][2,9]phenanthrolines: Synthesis, сharacterization, optical properties and light-induced electron transfer in composites with the semiconducting polymer MEH-PPV
    Synthetic Metals, V. 201, Pp. 43-48, MAR 2015. doi:10.1016/j.synthmet.2015.01.012, IF=2.252

Тезисы докладов на конференциях


    2019
  1. A. Sonina
    Stimuli responsive aggregation induced emission of fluore-vlidene capped thiophenephenylene co-oligomer single crystals
    VII-ая Международная летняя школа для молодых учёных RACIRI-2019, 04-09 Авгут 2019, Светлогорск, РФ
  2. E. Tretyakov, N. Troshkova, Yu. Ten, A. Keerthi, M. Baumgarten, A. Narita, K. Mullen, M. Slota, L. Bogani
    Design of Magnetic Edge States in Graphene Nanoribbons
    2nd Global Conference on Magnetism and Magnetic Materials, July 25-26, 2019, Rome, Italy
  3. E. Tretyakov, N. Troshkova, Yu. Ten, A. Keerthi, M. Baumgarten, A. Narita, K. Mullen, M. Slota, L. Bogani
    Design of Magnetic Edge States in Graphene Nanoribbons
    2nd Global Conference on Magnetism and Magnetic Materials, July 25-26, 2019, Rome, Italy
  4. E. Tretyakov, N. Troshkova, Yu. Ten, A. Keerthi, M. Baumgarten, A. Narita, K. Mullen, M. Slota, L. Bogani
    Design of Magnetic Edge States in Graphene Nanoribbons
    2nd Global Conference on Magnetism and Magnetic Materials, July 25-26, 2019, Rome, Italy
  5. E. Tretyakov, N. Troshkova, Yu. Ten, A. Keerthi, M. Baumgarten, A. Narita, K. Mullen, M. Slota, L. Bogani
    Design of Magnetic Edge States in Graphene Nanoribbons
    2nd Global Conference on Magnetism and Magnetic Materials, July 25-26, 2019, Rome, Italy

Патенты

  1. М.Б. Плотников, О.И. Алиев, А.М. Анищенко, А.В. Сидехменова, О.И. Дунаева, Д.Г. Мажукин, Ю.А. Тен
    Средства, обладающие антирадикальной активностью
    Заявка 2018129122, приоритет от 08.08.2018, Патент RU 2 692 124 , Бюл. № 18, опубликовано: 21.06.2019