Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- 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
- 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
- R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
- 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
- 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
- I. Philippov, Yu. Gatilov, A. Sonina, A. Vorob’ev
Oxidative [3+2]Cycloaddition of Alkynylphosphonates with Heterocyclic N-Imines: Synthesis of Pyrazolo[1,5-a]Pyridine-3-phosphonates
Molecules 2022, 27(22), 7913 doi:10.3390/molecules27227913, IF=4.927
- 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
- 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
- K.S. Ivanov, T. Riesebeck, A. Skolyapova, I. Liakisheva, M.S. Kazantsev, A.A. Sonina, R. Yu Peshkov, E.A. Mostovich
P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones
The Journal of Organic Chemistry, 2022, 87, 5, 2456-2469 doi:10.1021/acs.joc.1c02379, IF=4.198
- A. D. Kuimov, Ch. S. Becker, A. A. Sonina, M. S. Kazantsev
Host-guest molecular doping guide for emissive organic semiconductor crystals
New J. Chem., 2022, 46(44), 21257-21267 doi:10.1039/D2NJ03916H, IF=3.925
- 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
- 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
- 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