Поздразделение:
Группа органических материалов для электроники (ГРОМ)
Руководитель:
нс(кхн), руководитель группы Мостович Евгений Алексеевич
Публикации (по IF ) сотрудников подразделения (БД НИОХ СО РАН)
- 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
- Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
Interacting networks of purely organic spin-1/2 dimers
J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
- 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
- Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
- 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
- E.A. Mostovich, Y. Borozdina, V. Enkelmann, K. Removic-Langer, B. Wolf, M. Lang, M. Baumgarten
_Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets
Cryst. Growth Des., 2012, V. 12. № 1, 54-59. doi:10.1021/cg201224g, IF=4.388
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
- 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
- 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
- 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
- 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
- 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
