Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. 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
    
2. 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
    
3. 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
    
4. 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
    
5. 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
    
6. 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
    
7. C. Becker, G. Roshchupkina, T. Rybalova, Yu. Gatilov, V. Reznikov
   Transformations of 2,2-dimethyl-2,4-dihydro-3H-pyrrol-3-on-1-oxide derivatives in the Vilsmeier-Haack reaction conditions
   Tetrahedron, 2008, V. 64, N 39, 9191-9196. doi:10.1016/j.tet.2008.07.070, IF=2.868
    
8. A. I. Taratayko, C.S. Becker,.I. A. Grigor’ev,Y. V. Gatilov, T. V. Rybalova, V. A. Reznikov
   Synthesis of 3,4-dihydro-2H-pyrrole 1-oxide based aldonitrones as potential spin trapping agents
   Arkivoc 2013, (iv), 272-290.full text doi:10.3998/ark.5550190.p008.159, IF=1.57
    
9. C. Becker, G. Roshchupkina, T. Rybalova, Yu. Gatilov, G. Romanenko, V. Reznikov
   Unexpected formation of polycyclic oxygen-containing spiro-heterocycles in the reactions of 2,4-dihydro-3H-pyrrol-3-one 1 oxides with benzaldehyde
   Mendeleev Commun., 2008, V. 18, N 6, Pp 297-299. doi:10.1016/j.mencom.2008.11.002, IF=0.73
    
10. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
    Synthesis of a bis-Phosphonic Acid Derivative of Trolox, a New Potential Antioxidant
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 785-786. doi:10.1007/s10600-013-0746-2, IF=0.598
     
11. K.S. Bekker, N.V. Chukanov, S.A. Popov, I.A. Grigor'ev
    Conjugates of Bisphosphonates with Derivatives of Ursolic, Betulonic, and Betulinic Acids
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 581-582. doi:10.1007/s10600-013-0680-3, IF=0.598
     
12. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
    Synthesis of a bisphosphonate derivative of folic acid
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 495-495. doi:10.1007/s10600-013-0646-5, IF=0.598
     
13. 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
     
14. К.С. Беккер, Г.И. Рощупкина, Т.В. Рыбалова, Ю.В. Гатилов, В.А. Резников
    Превращения сопряженных енаминов ряда имидазолидин-1-оксила в реакции Вильсмайера-Хаака
    Изв. АН, Сер. Хим., 2007, Т. 56, № 6, 1165-1170. (Transformations of conjugated enamines of the imidazolidine 1-oxide series in the Vilsmeier-Haack reaction/ Ch. S. Becker, G. I. Roshchupkina, T. V. Rybalova, Yu. V. Gatilov, V. A. Reznikov// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1210-1215 doi:10.1007/s11172-007-0183-0), IF=0.504
     
15. А.Б. Бурдуков, К.С. Беккер, Г.А. Степанов, А.Л. Богатырев, Н.В. Первухина, А.С. Богомяков, В.А. Резников
    Структура и магнитные свойства новых хелатных комплексов меди (II) и никеля(II) с нитроксильным радикалом этил-2-(1-оксил-2,2,5,5-тетраметилимидазолидин-4-илиден)-3-оксопропаноатом
    Журнал структурной химии, 2010, Т. 51, № 5, C. 951-956. (Structure and magentic properties of novel chelate complexes of copper(II) and nickel(II) with nitroxide radical ethyl-2-(1-oxyl-2,2,5,5-tetramethylimidazolidin-4-yliden)-3-oxopropanoate/ A.B. Burdukov, K.S. Bekker, G.A. Stepanov, A.L. Bogatyrev, N.V. Pervukhina, A.S. Bogomyakov, V.A. Reznikov// J STRUCT CHEM+, 2010, V. 51, N 5, pp 916-922.. doi:10.1007/s10947-010-0139-3), IF=0.453