Публикации (по IF ) сотрудников подразделения (БД НИОХ СО РАН)

1. M.M. Shmakov, S.A. Prikhod'ko, R.Yu. Peshkov, V.V. Bardin, N. Yu. Adonin
   Aryldifluoroboranes: Lewis acidity and catalytic activity in the alkylation of phenols
   Molecular Catalysis, V. 521, March 2022, 112202 doi:10.1016/j.mcat.2022.112202, IF=5.089
    
2. S. Wang, Ya.V. Zonov, V.M. Karpov, O.A. Luzina, T.V. Mezhenkova
   Carbonylation of Polyfluorinated 1-Arylalkan-1-ols and Diols in Superacids
   Molecules 2022, 27(24), 8757 doi:10.3390/molecules27248757, IF=4.927
    
3. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
   Перспективные точки роста и вызовы фторорганической химии
   Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
    
4. H.-J. Frohn, V.V. Bardin
   Reaction of Organylxenonium(II) Salts, [RXe][Y], with Organyl Iodides, R'I, in Anhydrous HF: Scope and Limitation of a New Synthetic Approach to Iodonium Salts, [RR'I][Y]
   Inorg. Chem., 2012, V. 51, N 4, 2616-2620. doi:10.1021/ic202576v, IF=4.6
    
5. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
   The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
   Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
    
6. V.N. Kovtonyuk, Yu.V. Gatilov, P.V. Nikul’shin, R.A. Bredikhin
   Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene
   Molecules 2021, 26(3), 526 doi:10.3390/molecules26030526, IF=4.411
    
7. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
   Metal-organic frameworks based on octafluorobiphenyl-4,4'-dicarboxylate: synthesis, crystal structure, and surface functionality
   Dalton Trans., 2018, V. 47, N 10, Pp. 3283-3297 doi:10.1039/C7DT04566B, IF=4.099
    
8. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
   Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
   J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
    
9. N.Yu. Adonin, H.-J. Frohn, V.V. Bardin
   (Fluoroorgano)fluoroboranes and –borates. 16. Preparation of Bis(perfluoroalkyl)dimethoxyborate and Bis(perfluoroalkyl)difluoroborate salts, M[(C_nF2n+1)₂BX₂] (M = K, Nme₄; X ≡OMe, F)
   Organometallics, 2007, V. 26, N 9, 2420-2425. doi:10.1021/om070090h, IF=3.63
    
10. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Structural diversity of zinc(II) coordination polymers with octafluorobiphenyl-4,4'-dicarboxylate based on mononuclear, paddle wheel and cuboidal units
    CrystEngComm, 2019, V. 21, N 15, Pp 2524-2533 doi:10.1039/C9CE00073A, IF=3.382
     
11. S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
    1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
    RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
     
12. N.Yu. Adonin, D.E. Babushkin, V.N. Parmon, V.V. Bardin, G.A. Kostin, V.I. Mashukov, H.J. Frohn
    The effect of N-heterocyclic carbene ligands in the palladium - catalyzed cross-coupling reaction of K[C6F5BF3] with aryl iodides and aryl bromides
    Tetrahedron, 2008, V. 64, N 25, 5920-5924. doi:10.1016/j.tet.2008.04.043, IF=2.868
     
13. S.A. Cherkasov, A.D. Semikina, P.M. Kaletina, Yu.F. Polienko, D.A. Morozov, A.M. Maksimov, I.A. Kirilyuk, E.G. Bagryanskaya, D. Parkhomenko
    The Kinetics of 1,3-Dipolar Cycloaddition of Vinyl Monomers to 2,2,5,5-Tetramethyl-3-imidazoline-3-oxides
    ChemPhysChem, 2021, V.86, N 8, Pp 1080-1086 doi:10.1002/cplu.202100266, IF=2.862
     
14. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, V. N. Parmon
    The influence of the nature of phosphine ligand on palladium catalysts for cross-coupling of weakly nucleophilic potassium pentafluorophenyltrifluoroborate with ArHal and PhCH2Hal (Hal=Br, Cl)
    Tetrahedron, 2014, V.70, N, 23, P. 3720-3725. doi:10.1016/j.tet.2014.04.019, IF=2.816
     
15. L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
    Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
    Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762
     
16. V. V. Bardin, A. Yu. Shabalin, N. Yu. Adonin
    Weakly nucleophilic potassium aryltrifluoroborates in palladium-catalyzed Suzuki-Miyaura reactions: relative reactivity of K[4-RC6F4BF3] and the role of silver-assistance in acceleration of transmetallation
    Beilstein J. Org. Chem. 2015, 11, 608-616. doi:10.3762/bjoc.11.68, IF=2.762
     
17. Н.Ю. Адонин, В.В. Бардин
    Полифторированные органические соединения бора
    Успехи химии, 2010, 79, № 9, 832-860 (Polyfluorinated organic compounds of boron/ N. Yu. Adonin, V. V. Bardin// Russ. Chem. Rev., 2010, V. 79, pp 757. doi:10.1070/RC2010v079n09ABEH004136), IF=2.72
     
18. M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
    Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
    Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65
     
19. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
     
20. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551