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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 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.
7 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.
8 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.
9 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
10 Kiseleva Yuliya Olegovna laboratory assistant 249 This email address is being protected from spambots. You need JavaScript enabled to view it.
PHD Students
11 Kuimov Anatoly Dmitrievich Junior Researcher 239, 240 330-73-87 3-68, 4-44


 

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 (2015 - 2021 )

Обзоры, статьи в научных журналах


    2020
  1. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
    Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
    Dalton Trans., 2020, Advance Article, first published on 04 Nov 2019 doi:10.1039/C9DT03849C, IF=4.052
  2. 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=3.077
  3. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=3.441

  4. 2019
  5. 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
  6. 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
  7. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsina, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    A Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, First published: 18 December 2019 doi:10.1002/chem.201904587, IF=5.16
  8. 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
  9. 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
  10. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
    The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
    Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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

  19. 2018
  20. 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
  21. 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
  22. 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
  23. 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
  24. 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
  25. 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
  26. 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
  27. 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

  28. 2017
  29. 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
  30. 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
  31. 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
  32. 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
  33. 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
  34. 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
  35. 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

  36. 2016
  37. 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
  38. 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

  39. 2015
  40. 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
  41. 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. D. Mazhukin, E. Zaytseva, Y. Ten, D. Shiomi, Y. Gatilov, A. Yu, K. Sugisaki, A. Bogomyakov, K. Sato, T. Takui, E. Bagryanskaya
    New trends in the chemistry of hybrid phenoxyl-nitroxides
    the 13th Japanese-Russian Workshop on “Open Shell Compounds and Molecular Spin Devices”, November 10-13, 2019, Awaji Island, Japan., 2AM06
  2. Y.F. Polienko, S.A. Dobrynin, D.A. Morozov, A.A. Gorodetsky, M.A. Tyumentsev, P.D. Gladkikh, D.A. Parkhomenko, I.A. Kirilyuk
    Reduction-resistant nitroxide spin probes for EPR Imaging
    Book of abstracts XIth International Workshop on EPR in Biology and Medicine, Krakow, Poland, October 6-10, 2019, p. 91
  3. M. Kazantsev, A. Sonina, A. Kuimov, I. Koskin, T. Rybalova, I. Shundrina, C. Becker, E. Mostovich
    Highly-emissive semiconductors based on furan/phenylenes
    V Школа-конференция молодых ученых «Неорганические соединения и функциональные материалы» ICFM–2019, 30 сентября-4 октября, Новосибирск, , Сб. тезисов, С. 7
  4. E.G. Bagryanskaya, O.A. Krumkacheva, G. Shevelev, A. Lomzov, N. Dyrkheeva, A.A. Kuzhelev, V.M. Tormyshev, Yu. Polienko, M. Fedin, D. Pyshnyi, O. Lavrik, A. Chubarov, T. Godovikova
    DNA and RNA Complexes with Human Proteins : Structural Insights revealed by Pulsed Dipolar EPR with Orthogonal Spin Labeling
    Int. Conference "Magnetic Resonance - Current State and Future Perspectives" and satellite XXI International Youth Scientific School "Actual problems of magnetic resonance and its application", September 23-27, 2019 Kazan, Russia, , Book of Abst. P. 136
  5. Yu. Ten, N. Troshkova, E. Tretyakov
    A novel synthetic approach to alkylated 1,3-diphenyl-2-propanones –key building blocks in design of graphene nanostructures
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. PP-42, page 98
  6. I. Kurganskii, D. Votkina, P. Petunin, P. Postnikov, M. Trusova, E. Martynko, M. Kazantsev, Yu. Polienko, E. Bagryanskaya, E. Tretyakov, M. Fedin
    EPR Study of Nitroxyl-Verdazyl biradicals
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. PP-35, page 91
  7. A. Sonina, I. Koskin, P. Sherin, T. Rybalova, E. Mostovich, M. Kazantsev
    Stimuli responsive aggregation-induced emission of fluoren-ylidene capped thiophene/phenylene co-oligomer single crystal
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. PP-23, page 79
  8. A. Skolyapova, M. Kazantsev, E. Mostovich
    Synthesis of fluorinated derivatives of benzo[1,2-b:4,5-b']bisbenzofuran
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. PP-22, page 78
  9. E.A. Radiush, N.A. Semenov, E.A. Chulanova, A.V. Zibarev
    Charge transfer chemistry of novel strong electron acceptor –5,6-Dicyano-1,2,5-selenadiazolo[3,4-b]pyrazine
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. PP-21, page 77
  10. A.D. Kuimov, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, M.S. Kazantsev
    Doping offuran/phenylene co-oligomer single crystals as an efficient way to control their optoelectronic performance
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. PP-15, page 70
  11. N.A. Semenov, E.A. Radiush, E.A. Chulanova, L.A. Shundrin, I.Yu. Bagryanskaya, N.P. Gritsan, A.V. Zibarev
    1,2,5-chalcogenadiazoles -efficient electron acceptors for the design of paramagnetics and anion receptors
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. O-11, page 48
  12. D. Nevostruev, D. Baranov, V. Zinoviev, E. Glebov, M. Kazantsev, L. Kulik
    Organic solar cells based on novel acceptor anthrathiophene molecules: vacuum-free fabrication
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. O-7, page 45
  13. I. Koskin, E. Mostovich, E. Benass, M. Kazantsev
    Quantitative Topological Descriptor for Linear Co-oligomers Fusion
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. O-3, page 40
  14. E. Zaytseva, D. Shiomi, Yu. Ten, Yu. Gatilov, D. Stass, A. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E. Bagryanskaya, D. Mazhukin
    Magnetic properties of π-conjugated phenoxyl-nitroxide radicals as designed for advanced molecular magnetism
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. O-1, page 38
  15. E. Tretyakov, N. Troshkova, Yu. Ten, A. Keerthi, M. Baumgarten, A. Narita, K. Mullen, M. Slota, L. Bogani
    Spin-labeled graphene nanoribbons for organic electronics and spintronics
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. K-12, page 35
  16. M. Kazantsev, A. Sonina, A. Kuimov, I. Koskin, T. Rybalova, I. Shundrina, C. Becker, E. Mostovich
    Highly-Emissive Semiconductors Based on Furan/Phenylenes
    International conference ORGEL-2019, 23-29 Sept., Novosibirsk, Russia, Book of abst. K-5, page 28
  17. A.A. Sonina, A.D. Kuimov, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, M.S. Kazantsev
    Crystallization and Structures of Dibenzofulvene-based Derivatives,Crystallization and Structures of Dibenzofulvene-based Derivatives
    5th International Fall School on Organic Electronics, Moscow region, Russia, 15-20 Sept.2019, Book of Abstracts, p. 114
  18. 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
    5th International Fall School on Organic Electronics, 15-20 сентября 2019, Подмосковье, Россия, Book of Abstracts, p. 113
  19. A.D. Kuimov, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, M.S. Kazantsev
    Doping of Furan/Phenylene Co-oligomer Single Crystalsas an Efficient Wayto Control TheirOptoelectronic Performance
    5th International Fall School on Organic Electronics, Moscow region, Russia, 15-20 Sept.2019, Book of Abstracts, p. 100
  20. I.P. Koskin, E. Benassi, E.A. Mostovich, M.S. Kazantsev
    Computational Study of a Novel AIE Luminogen bis(4-((9H-fluoren-9lidene)methyl)phenyl)thiophene
    5th International Fall School on Organic Electronics, Moscow region, Russia, 15-20 Sept.2019, Book of Abstracts, p. 98
  21. I. Koskin, E. Mostovich, E. Benassi, M. Kazantsev
    Quantitative Topological Descriptor for Linear Co-oligomers Fusion
    5th International Fall School on Organic Electronics, Moscow region, Russia, 15-20 Sept.2019Book of Abstracts, p. 44
  22. A.A. Sonina, P.S. Sherin, T.V. Rybalova, E.A. Mostovich, M.S. Kazantsev
    Stimuli Responsive Aggregation-Induced Emission of Bis(4-((9H-fluoren-9ylidene)methyl)phenyl)thiophene Single Crystals
    5th International Fall School on Organic Electronics, Moscow region, Russia, 15-20 Sept.2019, Book of Abstracts, p. 53
  23. A. Sonina
    Stimuli responsive aggregation induced emission of fluore-vlidene capped thiophenephenylene co-oligomer single crystals
    RACIRI Summer School 2019: Structure, Real-time Dynamics and Processes in Complex Systems, Svetlogorsk, Russia, 04-11 August 2019, Book of Abstracts, p. 70.
  24. 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
  25. A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich, M.S. Kazantsev
    Stimuli Responsive Aggregation-Induced Emission of Bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene Single Crystals
    Tools for Chemical Bonding, July 14, 2019 - July 19, 2019 in Bremen, Germany, Book of Abstarcts, p. 20
  26. E.A. Radiush, N.A. Semenov, E.A. Chulanova, A.V. Zibarev
    Charge transfer chemistry of novel strong electron acceptor - 5,6-dicyano-1,2,5-selenadiazolo[3,4-b]pyrazine,
    International Workshop Tools for Chemical Bonding 2019, Bremen, Germany, July 14-19, Book of Abstracts, p. 15.
  27. 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 cooligomers
    Tools for Chemical Bonding, July 14, 2019 - July 19, 2019 in Bremen, Germany, Book of Abstarcts, p. 4
  28. E. Zaytseva, Yu. Ten, Yu. Gatilov, Ai. Yu, D. Mazhukin, E. Bagryanskaya
    Hybrid Phenoxyl-Nitroxide Radicals as a New Building Block in Magnetochemistry
    The 52nd Annual International Meeting of the ESR Spectroscopy Group of the Royal Society of Chemistry, April , 7- 11, 2019, Glasgow, UK, Book of Abst., P1.

Патенты

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