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Новосибирский институт органической химии им. Н.Н. Ворожцова
Сибирского отделения Российской академии наук

Поздразделение:  Лаборатория галоидных соединений (ЛГС)
Руководитель:  зав. лабораторий(дхн) Меженкова Татьяна Владимировна


 

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

  1. 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
     
  2. 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
     
  3. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, Vl.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
     
  4. 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
     
  5. 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[(CnF2n+1)2BX2] (M = K, Nme4; X ≡OMe, F)
    Organometallics, 2007, V. 26, N 9, 2420-2425. doi:10.1021/om070090h, IF=3.63
     
  6. 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
     
  7. 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
     
  8. 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
     
  9. 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
     
  10. 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
     
  11. 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
     
  12. 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
     
  13. 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
     
  14. 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
     
  15. H.-J. Frohn, V. V. Bardin
    Organoethynylxenon(II) tetrafluoroborates, [RC≡OCXe][BF4] - first examples of isolated alkynylxenonium salts: preparation and multi-NMR characterisation
    Eur. J. Inorg. Chem., 2006, N 19, 3948-3953. doi:10.1002/ejic.200600366, IF=2.509
     
  16. A.Y. Shabalin, N.Y. Adonin, V.V. Bardin
    Substitution of fluorine in M[C6F5BF3] with organolithium compounds: Distinctions between O- and N-nucleophiles
    Beilstein Journal of Organic Chemistry, 2017, 13, с. 703-713 doi:10.3762/bjoc.13.69, IF=2.336
     
  17. V.V. Bardin
    Synthesis of bis(pentafluorophenyl)phenylhalogenogermanes and bis(pentafluorophenyl)dihalogenogermanes, (C6F5)2GeXY (X = Ph, Y = Br, Cl; X = Y = F, Cl, Br)
    Journal of Organometallic Chemistry, 2016, V. 822, Pp 46-52 doi:10.1016/j.jorganchem.2016.08.014, IF=2.335
     
  18. T. V.Mezhenkova, V. V.Komarov,V. M.Karpov, I. V.Beregovaya,Ya.V.Zonov
    Synthesis of 1-(tetrafluorophenyl)perfluoro-1-phenylethanes and their cyclization into polyfluoro-9-methylfluorenes under the action of antimony pentafluoride
    Journal of Fluorine Chemistry, Available online 26 July 2020, 109615 doi:10.1016/j.jfluchem.2020.109615, IF=2.322
     
  19. V.V. Bardin, H.-J. Frohn
    Perfluoroorganylxenonium(II) salts from reactions of XeF2 or [FXe][SbF6] with selected perfluorinated alk-1-yn-1-yl- and alk-1-en-1-yltrifluoroborates in aHF
    J. Fluorine Chem., 2012, V. 138, 28-33. doi:10.1016/j.jfluchem.2012.03.014, IF=2.32
     
  20. V.M. Karpov, V.E. Platonov, T.V. Rybalova, Yu.V. Gatilov, M.M. Shakirov
    Fluorinated dihydroindeno[2,1-c][1,2,6]thiadiazines: the first synthesis, structural characterization and reactivity
    J. Fluorine Chem., 2012, V. 135, 254-260. doi:10.1016/j.jfluchem.2011.12.005, IF=2.32
     


 

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