Сотрудник:
Мостович Евгений Алексеевич
Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- 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
- 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
- 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.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,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
- 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
- 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
- E.A. Mostovich, D.G. Mazhukin, T.V. Rybalova
Reaction of vicinal aliphatic bis(hydroxylamines) with trifunctionalized methane derivatives
ARKIVOC, 2011, (xi), 29-42. doi:10.3998/ark.5550190.0012.b03, IF=1.95
- E.A. Mostovich, D.G. Mazhukin, Yu.V. Gatilov, T.V. Rybalova
Coupling of 1,2-bis(alkoxyamino)cyc-lohexane with 1,3-dicarbonyl com-pounds: first synthesis of 1,4-dialk-oxy-2,3-dihydro-1,4-diazepinium salts
Mendeleev Commun., 2007, V. 17, N 1, 48-50. doi:10.1016/j.mencom.2007.01.019, IF=0.712
