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Публикации кафедры ФОХ 2020 года

Обновлено

  1. N. A. Bokach, D. S. Bolotin, V. Yu. Kukushkin, Nonaromatic nitrogen heterocycles derived from metal-involving reactions of oximes, Chapter 16, in “Synthetic Approaches to Nonaromatic Nitrogen Heterocycles”, Wiley, 2020; accepted for publication.
  2. N. A. Bokach, D. S. Bolotin, V. Yu. Kukushkin, Metal-catalyzed and metal-mediated reactions of nitrones leading to nonaromatic nitrogen heterocyclic systems, Chapter 17, in “Synthetic Approaches to Nonaromatic Nitrogen Heterocycles”, Wiley, 2020; accepted for publication.
  3. V. Rozhkov, S. N. Eliseeva, S. Baykov, L. E. Zelenkov, D. Goryachii, I. V. Taydakov, Copper(I) ionic complexes based on imidazo[4,5-f][1,10]phenanthrolin diimine chelating ligands: crystal structures, photo- and electroluminescent properties, New J. Chem., 44 (2020) 110–120; DOI: 10.1039/C9NJ05109K.
  4. A. A. Eliseeva, D. M. Ivanov, A. S. Novikov, A. V. Rozhkov, I. V. Kornyakov, A. Yu. Dubovtsev, V. Yu. Kukushkin, Hexaiododiplatinate(II) as a useful supramolecular synthon for halogen bond involving crystal engineering, Dalton Trans., 49 (2020) 356–367; DOI: 10.1039/C9DT04221K.
  5. A.Yu. Dubovtsev, N.V. Shcherbakov, D.V. Dar’in, V.Yu. Kukushkin, Nature of the Nucleophilic Oxygenation Reagent is Key to Acid-Free Gold-Catalyzed Conversion of Terminal and Internal Alkynes to 1,2-Dicarbonyls, J. Org. Chem., 85 (2020) 745–757; DOI: 10.1021/acs.joc.9b02785.
  6. S. V. Baykov, S. I. Filimonov, A. V. Rozhkov, A. S. Novikov, I. V. Ananyev, D. M. Ivanov, V. Yu. Kukushkin, Reverse Sandwich Structures from Interplay between Lone pair–π-hole Atom-directed C•••dz2[M] and Halogen Bond Interactions, Cryst. Growth Des., (2020) In press; DOI: 10.1021/acs.cgd.9b01334.
  7. M. V. Il’in, L. A. Lesnikova, D. S. Bolotin, A. S. Novikov, V. V. Suslonov, V. Yu. Kukushkin, One-pot Route to N-acyl Ureas: a Formal Four-Component Hydrolytic Reaction Involving Aminonitrones and Isocyanide Dibromides, New. J. Chem., 44 (2020), 1253-1262; DOI: 10.1039/C9NJ05445F.
  8. A.V. Chupina, V.R. Shayapov, A.S. Novikov, V.V. Volchek, E. Benassi, P.A. Abramov, M.N. Sokolov,[{AgL}2Mo8O26]n– complexes: combined experimental and theoretical study, Dalton Trans., (2020) In press; DOI: 10.1039/C9DT04043A.
  9. V. Rozhkov, D. M. Ivanov, A. S. Novikov, I. V. Ananyev, N. A. Bokach, V. Yu. Kukushkin, Metal-involving halogen bond Ar–I∙∙∙[dz2PtII] in the platinum acetylacetonate complex, CrystEngComm, 22 (2020), 554-563; DOI: 10.1039/C9CE01568J.
  10. S.A. Adonin, M.A. Bondarenko, A.S. Novikov, P.E. Plyusnin, I.V. Korolkov, M.N. Sokolov, V.P. Fedin, Five new Sb(V) bromide complexes and their polybromide derivatives with pyridinium-type cations: structures, thermal stability and features of halogen•••halogen contacts in solid state, Inorg. Chim. Acta, (2020) In press. DOI: 10.1016/j.ica.2019.119278.
  11. S.A. Adonin, A.S. Novikov, K.V. Chernova, D.A. Vinnik, S.V. Taskaev, I.V. Korolkov, E.V. Ilyina, A.A. Pavlov, V.V. Novikov, M.N. Sokolov, V.P. Fedin, Heteroleptic copper(II) complexes with 2-bromo-5-methylpyridine: structures, features of non-covalent interactions and magnetic behavior, Inorg. Chim. Acta, 502 (2020) 119333; DOI: 10.1016/j.ica.2019.119333.
  12. O.V. Repina, A.S. Novikov, O.V. Khoroshilova, A.S. Kritchenkov, A.A. Vasin, A.G. Tskhovrebov, Lasagna-like supramolecular polymers derived from the PdII osazone complexes via C(sp2)–H•••Hal hydrogen bonding, Inorg. Chim. Acta, 502 (2020) 119378; DOI: 10.1016/j.ica.2019.119378.
  13. I.D. Gorokh, S.A. Adonin, A.N. Usoltsev, A.S. Novikov, D.G. Samsonenko, S.V. Zakharov, M.N. Sokolov, V.P. Fedin, Bromide complexes of bismuth with 4-bromobenzyl-substituted cations of pyridinium family, J. Mol. Struct., 1199 (2020) 126955; DOI: 10.1016/j.molstruc.2019.126955.
  14. E.A. Kostenko, S.V. Baykov, A.S. Novikov, V.P. Boyarskiy, Nucleophilic properties of the positively charged metal center in the solid state structure of palladium(II)-terpyridine complex, J. Mol. Struct., 1199 (2020) 126957; DOI: 10.1016/j.molstruc.2019.126957.
  15. A.M. Afanasenko, A.S. Novikov, T.G. Chulkova, Y.M. Grigoriev, I.E. Kolesnikov, S.I. Selivanov, G.L. Starova, A.A. Zolotarev, A.N. Vereshchagin, M.N. Elinson, Intermolecular interactions-photophysical properties relationships in phenanthrene-9,10-dicarbonitrile assemblies, J. Mol. Struct., 1199 (2020) 126789; DOI: 10.1016/j.molstruc.2019.07.036.
  16. K.G. Nikolaev, S.A. Ulasevich, O. Luneva, O.Yu. Orlova, D. Vasileva, S. Vasilev, A.S. Novikov, E.V. Skorb, Humidity-driven transparent holographic free-standing polyelectrolyte films, ACS Appl. Polym. Mater., (2020) In press. DOI: 10.1021/acsapm.9b01151.
  17. A.S. Mikherdov, S.A. Katkova, A.S. Novikov, M.M. Efremova, E.Yu. Reutskaya, M.A. Kinzhalov, (Isocyano group)•••lone pair interactions involving coordinated isocyanides: experimental, theoretical and CSD study, CrystEngComm, (2020) In press. DOI: 10.1039/C9CE01741K.
  18. D.S. Bolotin, N.S. Soldatova, M.Y. Demakova, A.S. Novikov, D.M. Ivanov, I.S. Aliyarova, A. Sapegin, M. Krasavin, Pentacoordinated silver(I) complex featuring 8-phenylquinoline ligands: interplay of coordination bonds, semicoordination, and stacking interactions, Inorg. Chim. Acta, (2020) In press. DOI: 10.1016/j.ica.2020.119453.
  19. V.Y. Mikshiev, A.F. Pozharskii, A. Filarowski, A.S. Novikov, A.S. Antonov, P.M. Tolstoy, M.A. Vovk, O.V. Khoroshilova, How strong is hydrogen bonding to amide nitrogen?, ChemPhysChem, (2020) In press. DOI: 10.1002/cphc.201901104.
  20. А. Н. Усольцев, С. А. Адонин, А. С. Новиков, М. Н. Соколов, В. П. Федин, Двухмерный координационный полимер {[Bi(Рyz)I3]}: строение и анализ упаковки методом поверхностей Хиршфельда, Коорд. хим., 46 (2020) 26–30; DOI: 10.31857/S0132344X20010089.
  21. С. А. Адонин, А. С. Новиков, В. П. Федин, Кристаллическая структура гетеролигандного комплекса [(2-Br-5-MePy)2CoCl2]·(2-Br-5-MePy): образование супрамолекулярных ассоциатов за счет галогенной связи, Коорд. хим., 46 (2020) 40–44; DOI: 10.31857/S0132344X20010016.
  22. С. А. Адонин, А. С. Новиков, В. П. Федин, Гетеролептические биядерные иодоацетатные комплексы меди(II) с 3-бромпиридином и 4-этилпиридином: кристаллические структуры и особенности контактов галоген···галоген, Коорд. хим., 46 (2020) 112–116; DOI: 10.31857/S0132344X20020012.
  23. Z. M. Efimenko, A. S. Novikov, D. M. Ivanov, A. V. Piskunov, A. A. Vereshchagin, O. V. Levin, N. A. Bokach, V. Yu. Kukushkin, The (dioximate)NiII/I2 system: ligand oxidation and binding modes of triiodide species, Inorg. Chem., 59 (2020), in press; doi: 10.1021/acs.inorgchem.9b03132.
  24. A. A. Eremina, M. A. Kinzhalov, E. A. Katlenok, A. S. Smirnov, E. V. Andrusenko, E. A. Pidko, V. V. Suslonov, K. V. Luzyanin, Phosphorescent Iridium(III) Complexes with Acyclic Diaminocarbene Ligands as Chemosensors for Mercury Inorg. Chem., 59 (2020) 2209-2222; DOI: 10.1021/acs.inorgchem.9b02833.
  25. A.N. Usoltsev, S.A. Adonin, A.S. Novikov, P.A. Abramov, M.N. Sokolov, V.P. Fedin, Chlorotellurate(IV) supramolecular associates with “trapped” Br2: features of non-covalent halogen•••halogen interactions in crystalline phases, CrystEngComm, (2020) In press. DOI: 10.1039/C9CE01820D.
  26. S.A. Adonin, A.N. Usoltsev, A.S. Novikov, B.A. Kolesov, V.P. Fedin, M.N. Sokolov, One- and two-dimensional iodine-rich iodobismuthate(III) complexes: structure, optical properties and features of halogen bonding in solid state, Inorg. Chem., (2020) In press. DOI: 10.1021/acs.inorgchem.9b03734.
  27. V.N. Mikhaylov, V.N. Sorokoumov, A.S. Novikov, M.V. Melnik, A.G. Tskhovrebov, I.A. Balova, Intramolecular hydrogen bonding stabilizes trans-configuration in a mixed carbene/isocyanide PdII complexes, J. Organomet. Chem., (2020) In press. DOI: 10.1016/j.jorganchem.2020.121174.
  28. A. V. Buldakov, M. A. Kinzhalov, M. A. Kryukova, D. M. Ivanov, A. S. Novikov, A. S. Smirnov, G. L. Starova, N. A. Bokach and V. Y. Kukushkin, Isomorphous Series of PdII-Containing Halogen Bond Donors Exhibiting Cl/Br/I Triple Halogen Isostructural Exchange. Cryst. Growth Des. (2020) In press. DOI: 10.1021/acs.cgd.9b01631.
  29. O. Zaitceva, V. Bénéteau, D. S. Ryabukhin, I. I. Eliseev, M. A. Kinzhalov, B. Louis, A. V. Vasilyev and P. Pale, Cyclization of aryl 3-aryl propynoates into 4-arylcoumarins catalyzed by cyclometalated Platinum(II) complexes. Tetrahedron (2020), 131029. DOI: 10.1016/j.tet.2020.131029.
  30. A.N. Usoltsev, A.S. Novikov, B.A. Kolesov, K.V. Chernova, P.E. Plyusnin, V.P. Fedin, M.N. Sokolov, S.A. Adonin, Halogen•••halogen contacts in triiodide salts of pyridinium-derived cations: theoretical and spectroscopic studies, J. Mol. Struct., (2020) In press. DOI: 10.1016/j.molstruc.2020.127949.
  31. I.N. Klyukin, A.S. Novikov, A.P. Zhdanov, K.Yu. Zhizhin, N.T. Kuznetsov, Theoretical study of monocarbonyl derivatives of closo-borate anions [BnHn–1CO]– (n = 6, 10, 12): bonding and reactivity analysis, Mendeleev Commun., 30 (2020) 88–90; DOI: 10.1016/j.mencom.2020.01.029.
  32. M.M. Efremova, A.P. Molchanov, A.S. Novikov, G.L. Starova, A.A. Muryleva, A.V. Slita, V.V. Zarubaev, 1,3-Dipolar cycloaddition of N-allyl substituted polycyclic derivatives of isoindole-1,3-dione with nitrones and nitrile oxides: An experimental and theoretical investigation, Tetrahedron, (2020) In press. DOI: 10.1016/j.tet.2020.131104.
  33. A. Pulyalina, I. Faykov, V. Nesterova, M. Goikhman, I. Podeshvo, N. Loretsyan, A. Novikov, I. Gofman, A. Toikka, G. Polotskaya, Novel polyester amide membranes containing biquinoline units and complex with Cu(I): synthesis, characterization, and approbation for n-heptane isolation from organic mixtures, Polymers, 12 (2020) 645; DOI: 10.3390/polym12030645.
  34. T. V. Serebryanskaya, M. A. Kinzhalov, V. Bakulev, G. Alekseev, A. Andreeva, P. V. Gushchin, A. Protas, A. Smirnov, T. L. Panikorovskii, P. Lippmann, I. Ott, C. M. Verbilo, A. Zuraev, A. S. Bunev, V. Boyarskiy and N. A. Kasyanenko, Water Soluble Palladium(II) and Platinum(II) Acyclic Diaminocarbene Complexes: Solution Behavior, DNA Binding, and Antiproliferative Activity, New J. Chem., (2020), in press, DOI 10.1039/D1030NJ00060D.
  35. A.S. Ostras’, D.M. Ivanov, A.S. Novikov, P.M. Tolstoy, Phosphine oxides as spectroscopic halogen bond descriptors: IR and NMR correlations with interatomic distances and complexation energy, Molecules, 25 (2020) 1406; DOI: 10.3390/molecules25061406.
  36. N. S. Soldatova, V. V. Suslonov, T. Yu. Kissler, D. M. Ivanov, A. S. Novikov, M. S. Yusubov, P. S. Postnikov, V. Yu. Kukushkin, Halogen bonding provides heterooctameric supramolecular aggregation of diaryliodonium thiocyanate, Crystals, 10 (2020) 230; doi:10.3390/cryst10030230.
  37. E. A. Katlenok, M. Haukka, O. V. Levin, A. Frontera, V. Yu. Kukushkin, Supramolecular assembly of metal complexes by (Aryl)I···dz2[PtII] halogen bond, Chem. Eur. J., 26 (2020) 7692–7701; doi: 10.1002/chem.202001196.
  38. L. E. Zelenkov, M. L. Kuznetsov, E. V. Andrusenko, M. S. Avdontceva, G. L. Starova, N. A. Bokach, V. Yu. Kukushkin, Nickel(II)-mediated cyanamide–pyrazole coupling highlights distinct reactivity of NCNR2 and NCR nitrile ligands, New J. Chem., 44 (2020) 6979–6991, doi: 10.1039/D0NJ00704H.
  39. S.N. Yunusova, A.S. Novikov, O.V. Khoroshilov, I.E. Kolesnikov, M.Ya. Demakova, D.S. Bolotin, Solid-state fluorescent 1,2,4-triazole zinc(II) complexes: self-organization via bifurcated (N–H)2•••Cl contacts, Inorg. Chim. Acta, (2020) In press. DOI: 10.1016/j.ica.2020.119660.
  40. М.А. Бондаренко, С.А. Адонин, А.С. Новиков, М.Н. Соколов, В.П. Федин, Супрамолекулярный полибромид-бромоанимонат(V) (2,6-BrPyH)3[SbBr6]{(Br2)Br}•2H2O: особенности контактов галоген•••галоген в кристаллической структуре, Коорд. хим., 46 (2020) 264; DOI: 10.31857/S0132344X20040015.
  41. S.A. Adonin, M.A. Bondarenko, A.S. Novikov, M.N. Sokolov, Halogen bonding in isostructural Co(II) complexes with 2-halopyridines, Crystals, 10 (2020) 289; DOI: 10.3390/cryst10040289.
  42. A. Paul, L.M.D.R.S. Martins, A. Karmakar, M.L. Kuznetsov, A.S. Novikov, M.F.C. Guedes da Silva, A.J.L. Pombeiro, Environmentally benign benzyl alcohol oxidation and C-C coupling catalysed by amide functionalized 3D Co(II) and Zn(II) metal organic frameworks, J. Catal., 385 (2020) 324; DOI: 10.1016/j.jcat.2020.03.035.
  43. O. V. Mikolaichuk, A.V. Protas, E.A. Popova, A.S. Mikherdov, I.V. Kornyakov, R.E. Trifonov, Novel tris(5‐aryl‐1H‐tetrazol‐1‐yl)methanes and 2‐dichloromethyl‐5‐aryl‐2H‐tetrazoles and noncovalent interactions in their crystal structure, J. Heterocyclic. Chem., (2020), In press; DOI: 10.1002/jhet.3969.
  44. D.M. Ivanov, S.V. Baykov, A.S. Novikov, G. Romanenko, N.A. Bokach, R.A. Evarestov, V.Yu. Kukushkin, Noncovalent sulfoxide–nitrile coupling involving four center heteroleptic dipole–dipole interactions between the sulfinyl and nitrile groups, Cryst. Growth Des. 20 (2020) 3417–3428; doi: 10.1021/acs.cgd.0c00196.
  45. D.S. Bolotin, M.V. Il’in, V.V. Suslonov, A.S. Novikov, Symmetrical noncovalent interactions Br•••Br observed in crystal structure of exotic primary peroxide, Symmetry, 12 (2020) 637; DOI: 10.3390/sym12040637.
  46. M. V. Dobrynin, V. Yu. Kukushkin, R. M. Islamova, Cellulose-based hybrid glycosilicones via grafted-to metal-catalyzed hydrosilylation: “when opposites unite”, Carbohydrate Polymers, 241 (2020) 116327; doi: 10.1016/j.carbpol.2020.116327.
  47. I. V. Ananyev, N. A. Bokach, V. Yu. Kukushkin, Structure-directing sulfur···metal noncovalent semicoordination bonding, Acta Crystallogr., Section B, B76 (2020) 436–449; doi: 10.1107/S2052520620005685.
  48. A. Yu. Dubovtsev, N. V. Shcherbakov, D. V. Dar’in, V. Yu. Kukushkin, The Dichotomy of gold-catalyzed interplay between cyanamides and ynamides: controllable switch from [2+2+2] to [4+2] cycloaddition, Adv. Synth. & Catal., 362 (2020) in press; doi: 10.1002/adsc.202000434.
  49. D. A. Shabalin, A. Yu. Dubovtsev, E. Yu. Schmidt, B. A. Trofimov, Calcium carbide as acetylene source in cascade assemblies of hydroxypyrrolines and 3H-pyrroles from ketoximes, ChemistrySelect, 5 (2020) 3434–3437; DOI: 10.1002/slct.202000392.
  50. V. V. Matveevskaya, D. I. Pavlov, T. S. Sukhikh, A. L. Gushchin, A. Yu. Ivanov, T. B. Tennikova, V. V. Sharoyko, S. V. Baykov, E. Benassi, A. S. Potapov, Arene−ruthenium(II) complexes containing 11H‑indeno[1,2‑b]quinoxalin-11-one derivatives and tryptanthrin-6-oxime: synthesis, characterization, cytotoxicity, and catalytic transfer hydrogenation of aryl ketones, ACS Omega, 2020, in press; DOI: 10.1021/acsomega.0c01204.
  51. M.A. Kryukova, A.V. Sapegin, A.S. Novikov, M. Krasavin, D.M. Ivanov, New crystal forms for biologically active compounds. Part 2: anastrozole as N-substituted 1,2,4-triazole in halogen bonding and lp-π interactions with 1,4-diiodotetrafluorobenzene, Crystals, 10 (2020) 371; DOI: 10.3390/cryst10050371.
  52. V. V. Suslonov, A. A. Eliseeva, A. S. Novikov, D. M. Ivanov, A. Yu. Dubovtsev, N. A. Bokach, V. Yu. Kukushkin, Tetrachloroplatinate(II) anion as a square-planar tecton for crystal engineering involving halogen bonding, CrystEngComm, 22 (2020) 4180-4189; doi: 10.1039/D0CE00576B.
  53. A. S. Mikherdov, A. S. Novikov, V. P. Boyarskiy, V. Yu. Kukushkin, The halogen bond with isocyano carbon reduces isocyanide odor, Nature Commun., 11 (2020) Article number 2921; doi: 10.1038/s41467-020-16748-x.
  54. A. V. Rozhkov, I. V. Ananyev, R. M. Gomila, A. Frontera, V. Yu. Kukushkin, π-Hole···dz2[PtII] interactions with electron-deficient arenes enhance phosphorescence of PtII-based luminophores, Inorg. Chem., 59 (2020) 9308–9314; doi: 10.1021/acs.inorgchem.0c01170.
  55. С.А. Адонин, А.С. Новиков, Ю.К. Смирнова, З.Р. Тушакова, В.П. Федин, Гетеролигандные комплексы Cu(II) с 2-галогенопиридинами: кристаллическая структура и особенности контактов галоген•••галоген в твердом теле, ЖСХ, 61 (2020) 753; DOI: 10.26902/JSC_id56616.
  56. A.S. Novikov, Why [2 + 2]-cycloaddition reactions between isocyanates and imines do not occur in Pd-activation conditions?, Inorg. Chim. Acta, (2020) In press. DOI: 10.1016/j.ica.2020.119758.
  57. E. E. Galenko, M. A. Kryukova, M. S. Novikov, A. F. Khlebnikov, J. Org. Chem., 85 (2020) 6109–6122; doi: 10.1021/acs.joc.0c00611.
  58. A. N. Gusev, E. V. Braga, M. A. Kryukova, N. V. Lubomirskii, E. A. Zamnius, V. F. Shulgin, Photoluminescence of the Coordination Zinc Compounds with 3-Methyl-4-Formyl-1-Phenylpyrazol-5-one Acylhydrazones, Russ. J. Coord. Chem., 46 (2020) 251–259; doi: 10.1134/S107032842004003X.
  59. V. A. Ivoplgina, M. S. Chernov’yants, L. D. Popov, V. V. Suslonov, N. A. Avtushenko, N. V. Luanguzov, Structural study and thermal behavior of novel interaction product of 4-amino-5-(furan-2-yl)-4H-1,2,4-triazole-3-thione with molecular iodine, Phosphorous, Sulfur, and Silicon and the Related Elements, 195 (2020), 421-428; doi: 10.1080/10426507.2019.1700414.
  60. N. Toikka, A. S. Mikherdov, D. M. Ivanov, T. J. Mooibroek, N. A. Bokach, V. Yu. Kukushkin, Cyanamides as π-hole donor components of structure-directing (сyanamide)···arene noncovalent interactions, Crystal Growth & Design, 20 (2020); doi: 10.1021/acs.cgd.0c00561.
  61. А.В. Нелюбин, Н.А. Селиванов, А.Ю. Быков, И.Н. Клюкин, А.С. Новиков, А.П. Жданов, К.Ю. Жижин, Н.Т. Кузнецов, N-борилированные гидроксиламины [B12H11NH2OH]– – новый тип замещенных производных клозо-додекаборатного аниона, ЖНХ, 65 (2020) 719-724; DOI: 10.31857/S0044457X20060136.
  62. A. V. Rozhkov, A. A. Eliseeva, S. V. Baykov, B. Galmés, A. Frontera, V. Yu. Kukushkin, Building blocks for crystal engineering involving halogen bonding: one-pot route to X-perfluoroarenes (X = Br, I) based on FeIII-assisted C–F functionalization, Crystal Growth & Design, 20 (2020); doi: 10.1021/acs.cgd.0c00606.
  63. I.N. Klyukin, A.S. Novikov, A.P. Zhdanov, K.Yu. Zhizhin, N.T. Kuznetsov, Theoretical study of closo-borate derivatives of general type [BnHn-1COR]2– (n = 6, 10, 12; R = H, CH3, NH2, OH, OCH3) – borylated analogue of organic carbonyl compounds, Polyhedron, (2020) In press. DOI: 10.1016/j.poly.2020.114682.
  64. A.S. Novikov, Non-covalent interactions in coordination and organometallic chemistry, Crystals, 10 (2020) 537; DOI: 10.3390/cryst10060537.
  65. N.S. Soldatova, P. S. Postnikov, V. V. Suslonov, T. Yu. Kissler, D. M. Ivanov, M. S. Yusubov, B. Galmés, A. Frontera, V. Yu. Kukushkin, Diaryliodonium as a double σ-hole donor: the dichotomy of thiocyanate halogen bonding provides divergent solid state arylation by diaryliodonium cations, Org. Chem. Front., 7 (2020), 2230-2242; doi: 10.1039/D0QO00678E.
  66. A.N. Usoltsev, S.A. Adonin, B.A. Kolesov, A.S. Novikov, V.P. Fedin, M.N. Sokolov, Opening the third century of polyhalide chemistry: thermally stable complex with “trapped” dichlorine, Chem. Eur. J., (2020) In press. DOI: 10.1002/chem.202002014.
  67. T. K. Nguyen, G. D. Titov, O. V. Khoroshilova, M. A. Kinzhalov, N. V. Rostovskii, Light-induced one-pot synthesis ofpyrimidine derivatives from vinyl azides. Org. Biomol. Chem. (2020) Advance Article. DOI: 10.1039/D0OB00693A.
  68. A.N. Usoltsev, N.A. Korobeynikov, A.S. Novikov, V.R. Shayapov, I.V. Korolkov, D.G. Samsonenko, V.P. Fedin, M.N. Sokolov, S.A. Adonin, One-dimensional supramolecular hybrid iodobismuthate(1-EtPy)3{[Bi2I9](I2)0.75}: structural features and theoretical studies of I•••I non-covalent interactions, J. Clust. Sci., (2020) In press. DOI: 10.1007/s10876-020-01843-2.
  69. A.M. Afanasenko, T.G. Chulkova, I.A. Boyarskaya, R.M. Islamova, A.A. Legin, B.K. Keppler, S.I. Selivanov, A.N. Vereshchagin, M.N. Elinson, M. Haukka, C,N-Chelated diaminocarbene platinum(II) complexes derived from 3,4-diaryl-1H-pyrrol-2,5-diimines and cis-dichlorobis(isonitrile)platinum(II): synthesis, cytotoxicity, and catalytic activity in hydrosilylation reactions, J. Organomet. Chem., (2020) in press; DOI: 10.1016/j.jorganchem.2020.121435.
  70. E. Miliutina, O. Guselnikova, N. S. Soldatova, P. Bainova, R. Elashnikov, P. Fitl, T. Kurten, M. S. Yusubov, V. Švorčík, R. R. Valiev, M. M. Chehimi, O. Lyutakov, P. S. Postnikov, Can plasmon change reaction path? Decomposition of unsymmetrical iodonium salts as an organic probe, J. Phys. Chem. Lett., 11 (2020) 5770–5776. DOI: 10.1021/acs.jpclett.0c01350.
  71. A.N. Usoltsev, N.A. Korobeynikov, A.S. Novikov, P.E. Plyusnin, V.P. Fedin, M.N. Sokolov, S.A. Adonin, Hybrid chlorobismuthate(III) “trapping” Br2 unit: crystal structure and theoretical investigation of non-covalent Cl···Br interactions in (1-MePy)3{[Bi2Cl9](Br2)}, Inorg. Chim. Acta, (2020) In press. DOI: 10.1016/j.ica.2020.119932.
  72. V.V. Sharutin, O.K. Sharutina, A.S. Novikov, S.A. Adonin, Substituent-dependent reactivity of triarylantimony(III) toward I2: isolation of [Ar3SbI]+ salt, New J. Chem., (2020) In press. DOI: 10.1039/D0NJ02774J.
  73. S.V. Baykov, V.P. Boyarskiy, Metal-free functionalization of azine N-oxides with electrophilic reagents, Chem Heterocycl Compd., 56 (2020) 814–823; DOI: 10.1039/d0sc02970j.
  74. S. Baykov, A. Semenov, M. Tarasenko, V.P. Boyarskiy, Application of amidoximes for the heterocycles synthesis, Tetrahedron Lett., (2020) In press.; DOI: 10.1016/j.tetlet.2020.152403.
  75. L. E. Zelenkov, D. M. Ivanov, E. K. Sadykov, N. A. Bokach, B. Galmés, A. Frontera, V. Yu. Kukushkin, Semicoordination bond breaking and halogen bond making change the supramolecular architecture of metal-containing aggregates, Crystal Growth & Design, 20 (2020); doi: 10.1021/acs.cgd.0c00999.
  76. S. N. Yunusova, D. S. Bolotin, M. A. Vovk, P. M. Tolstoy, V. Yu. Kukushkin, Tetrabromomethane as an organic catalyst: a kinetic study of CBr4-catalyzed Schiff condensation, Eur. J. Org. Chem., 2020, accepted. doi: 10.1002/ejoc.202001180.
  77. A. G. Tskhovrebov, A. S. Novikov, A. S. Kritchenkov, V. N. Khrustalev, M. Haukka, Attractive halogen···halogen interactions in crystal structure of trans-dibromogold(III) complex, Z. Kristallogr. Cryst. Mater., 235 (2020) 477–480; DOI: 10.1515/zkri-2020-0045.
  78. A. N. Usoltsev, A. S. Novikov, M. N. Sokolov, S. A. Adonin, Neutral heteroleptic complexes of bis(2-halopyridine)dihalocopper(II) family: how the nature of halogen atom affects supramolecular motifs and energies of halogen bonding in solid state?, Solid State Sci., (2020) In press.; DOI: 10.1016/j.solidstatesciences.2020.106441.
  79. Д.В. Боярская, Т.Г. Чулкова, Влияние строения C,N-хелатных диаминокарбеновых комплексов палладия(II) на каталитическую активность в реакции Соногаширы, ЖОрХ, 56, 11 (2020) 1731-1736; doi: 10.31857/S0514749220110075.
  80. M. A. Bondarenko, A. S. Novikov, V. P. Fedin, M. N. Sokolov, S. A. Adonin, The stabilization of decabromide {Br10}2− anion in the structure of Sb(V) bromide complex, J. Coord. Chem., (2020) In press.; DOI: 10.1080/00958972.2020.1837785.
  81. V. G. Nenajdenko, N. G. Shikhaliyev, A. M. Maharramov, K. N. Bagirova, G. T. Suleymanova, A. S. Novikov, V. N. Khrustalev, A. G. Tskhovrebov, Halogenated diazabutadiene dyes: synthesis, structures, supramolecular features, and theoretical studies, Molecules, 25 (2020) 5013; DOI: 10.3390/molecules25215013.
  82. A. N. Usoltsev, N. A. Korobeynikov, A. S. Novikov, P. E. Plyusnin, B. A. Kolesov, V. P. Fedin, M. N. Sokolov, S. A. Adonin, One-dimensional diiodine–iodobismuthate(III) hybrids cat3{[Bi2I9](I2)3}: syntheses, stability, and optical properties, Inorg. Chem., (2020) In press.; DOI: 10.1021/acs.inorgchem.0c02599.
  83. A. S. Novikov, Computational insights into industrial chemistry, Computation, 8 (2020) 97; DOI: 10.3390/computation8040097.
  84. I. S. Dmitriev, V. Yu. Kukushkin, “Sublime generalization: discovery of the Periodic law”, a book chapter in Celebration of The Periodic Table of The Elements at The Academy of Sciences of Lisbon. A Chemistry Symposium, Coordinated by A.J.L. Pombeiro, Academia das Ciências de Lisboa Edition, 2020, pp. 8–24; e-book, ISBN 978-972-623-394-7.
  85. V. V. Shilovskikh, A. A. Timralieva, P. V. Nesterov, A. S. Novikov, P. A. Sitnikov, E. A. Konstantinova, A. I. Kokorin, E. V. Skorb, Melamine–barbiturate supramolecular assembly as a pH‐dependent organic radical trap material, Chem. Eur. J., (2020) In press.; DOI: 10.1002/chem.202002947.
  86. A. S. Novikov, Symmetry in quantum and computational chemistry, Symmetry, 12 (2020) 2028; DOI: 10.3390/sym12122028.
  87. N.A. Shcherbina, I.V. Kazakov, D.V. Spiridonova, V.V. Suslonov, O.V. Khoroshilova, V.N. Mikhailov, A.Y. Timoshkin, Reaction of In(C6F5)3Et2O with Complexes of Copper and Silver Monochlorides with N,N′-Bis(isopropylphenyl)imidazol-2-ylidene, Russian Journal of General Chemistry, 90 (2020), 2503-2508; DOI: 10.1134/S1070363220120440.