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Публикации кафедры ФОХ 2022 года

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  1. I. S. Aliyarova, E. Yu. Tupikina, D. M. Ivanov, V. Yu. Kukushkin, Metal-involving halogen bonding including gold(I) as a nucleophilic partner. The case of isomorphic dichloroaurate(I)∙halomethane cocrystals, Inorg. Chem., 61 (2022); doi: 10.1021/acs.inorgchem.1c03482.
  2. M. Nikishina, L. Perelomov, Y. Atroshchenko, E. Ivanova, L. Mukhtorov, P. Tolstoy, Sorption of fulvic acids and their compounds with heavy metal ions on clay minerals, Soil Syst., 6 (2022), 2; DOI: 10.3390/soilsystems6010002.
  3. D. M. Ivanov, N. A. Bokach, V. Yu Kukushkin, A. Frontera, Metal centers as nucleophiles: oxymoron of halogen bond-involving crystal engineering, Chem. Eur. J., 28 (2022) e202103173. DOI: 10.1002/chem.202103173.
  4. S. A. Katkova, A. S. Mikherdov, E. V. Sokolova, A. S. Novikov, G. L. Starova, M. A. Kinzhalov, Intermolecular (Isocyano group)×××PtII Interactions Involving Coordinated Isocyanides in Cyclometalated PtII Complexes, J. Mol. Struct., 1253 (2022) 132230. DOI: 10.1016/j.molstruc.2021.132230.
  5. M. A. Bondarenko, P. A. Abramov, A. S. Novikov, M. N. Sokolov, S. A. Adonin, Cu(II) pentaiodobenzoate complexes: “super heavy carboxylates” featuring strong halogen bonding, Polyhedron 214 (2022) 115644; DOI: 10.1016/j.poly.2021.115644.
  6. 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, Eur. J. Inorg. Chem. (2022) In press.; DOI: 10.1002/ejic.202100890.
  7. N. F. Romashev, P. A. Abramov, I. V. Bakaev, I. S. Fomenko, D. G. Samsonenko, A. S. Novikov, K. K. H. Tong, D. Ahn, P. V. Dorovatovskii, Y. V. Zubavichus, A. A. Ryadun, O. A. Patutina, M. N. Sokolov, M. V. Babak, A. L. Gushchin, Heteroleptic Pd(II) and Pt(II) complexes with redox-active ligands: synthesis, structure, and multimodal anticancer mechanism, Inorg. Chem. (2022) In press.; DOI: 10.1021/acs.inorgchem.1c03314.
  8. V. Rozentsvet, N. Sablina, D. Ulyanova, S. Kostjuk, P. Tolstoy, Structure of terminal units of polybutadiene synthesized via anionic mechanism, Polym. Bull. 79 (2022), 1239-1256; DOI: 10.1007/s00289-021-03549-5.
  9. M. A. Kinzhalov, D. M. Ivanov, A. A. Melekhova, N. A. Bokach, A. Frontera, V. Yu. Kukushkin, Chameleonic metal-bound isocyanides: a π-donating CuI-center imparts nucleophilicity to the isocyanide carbon toward halogen bonding, Inorg. Chem. Front., 9 (2022) 1655–1665; doi: 10.1039/D2QI00034b.
  10. M.V. ll'in, A.A. Sysoeva, A.S. Novikov, D.S. Bolotin, Diaryliodoniums as Hybrid Hydrogen- and Halogen-Bond-Donating Organocatalysts for the Groebke–Blackburn–Bienaymé Reaction. J. Org. Chem., 87 (2022) 4569–4579; DOI:10.1021/acs.joc.1c02885.
  11. A. S. Novikov, Theoretical investigation on non-covalent interactions, Crystals 12 (2022) 167; DOI: 10.3390/cryst12020167.
  12. M. V. Grudova, A. S. Kubasov, V. N. Khrustalev, A. S. Novikov, A. S. Kritchenkov, V. G. Nenajdenko, A. V. Borisov, A. G. Tskhovrebov, Exploring supramolecular assembly space of cationic 1,2,4-selenodiazoles: effect of the substituent at the carbon atom and anions, Molecules 27 (2022) 1029; DOI: 10.3390/molecules27031029.
  13. A. S. Novikov, Non-covalent interactions in organic, organometallic, and inorganic supramolecular systems relevant for medicine, materials science, and catalysis, Crystals 12 (2022) 246; DOI: 10.3390/cryst12020246.
  14. V. A. Dodonov, O. A. Kushnerova, R. V. Rumyantsev, A. S. Novikov, V. K. Osmanov, I. L. Fedushkin, Cycloaddition of isoselenocyanates to sodium and magnesium metallacycles, Dalton Trans. (2022) In press.; DOI: 10.1039/D1DT04366H.
  15. V. V. Suslonov, N. S. Soldatova, P. S. Postnikov, G. Resnati, V. Yu. Kukushkin, D. M. Ivanov, N. A. Bokach, Diaryliodonium tetracyanometallates self-assemble into halogen bonded square-like arrays, Crystal Growth & Design, 22 (2022); doi: 10.1021/acs.cgd.2c00175.
  16. K. Sotiriadis, K. Aspiotis, A. Mazur, P. Tolstoy, E. Badogiannis, S. Tsivilis, Characterization of old concrete from a heritage structure of Inousses cluster of islands, Lect. Notes Civ. Eng., 209 (2022) 80–89; DOI: 10.1007/978-3-030-90788-4_7.
  17. F. Shakirova, U. Markova, P. Tolstoy, A. Bulatov, A. Shishov, A new hydrophobic deep eutectic solvent based on thymol and 4-(dimethylamino)benzaldehyde: derivatization and microextraction of urea, J. Mol. Liquids, 353 (2022) 118820; DOI: 10.1016/j.molliq.2022.118820.
  18. A. Mazur, P. Tolstoy, K. Sotiriadis, 13С, 27Al and 29Si NMR investigation of the hydration kinetics of Portland-limestone cement pastes containing CH3-COO–R+ (R=H or Na), Materials, 15 (2022) 2004; DOI: 10.3390/ma15062004.
  19. В. А. Розенцвет, Д. М. Ульянова, Н. А. Саблина, М. Г. Кузнецова, П. М. Толстой, Полимеризация 1,3-пентадиена под действием катионных каталитических систем на основе алюминийорганических соединений, Известия АН, 4 (2022), 787–795.
  20. M. A. Kostin, S. A. Pylaeva, P. M. Tolstoy, Phosphine oxides as NMR and IR spectroscopic probes for the estimation of the geometry and energy of hydrogen bonds: PO…H-A hydrogen bonds, Phys. Chem. Chem. Phys., 24 (2022) 7121–7133; DOI: 10.1039/D1CP05939D.
  21. V. A. Rozentsvet, D. M. Ulyanova, N. A. Sablina, S. V. Kostjuk, P. M. Tolstoy, I. A. Novakov, Cationic polymerization of butadiene using alkyl aluminum compounds as co-initiators: an efficient approach toward solid polybutadienes, Polym. Chem., 3 (2022) 1596–1607; DOI: 10.1039/d1py01684a.
  22. N. S. Soldatova, P. S. Postnikov, D. M. Ivanov, O. V. Semyonov, O. S. Kukurina, O. Guselnikova, Y. Yamauchi, T. Wirth, V. V. Zhdankin, M. S. Yusubov, R. M. Gomila, A. Frontera, G. Resnati, V. Yu. Kukushkin, Zwitterionic iodonium species afford halogen bond-based porous organic frameworks, Chemical Science, 2022, accepted.
  23. E. I. Chikunova, V. Yu Kukushkin, A. Yu. Dubovtsev, Atom-economic Synthesis of β-Ketosulfones Based on Gold-catalyzed Highly Regioselective Hydration of Alkynylsulfones, Green Chem., 2022, DOI: 10.1039/D2GC00541G.
  24. A. A. Yakubenko, A.M. Puzyk, V. O. Korostelev, V. V. Mulloyarova, E. Yu. Tupikina, P. M. Tolstoy, A. S. Antonov, Self-association of diphenylpnictoginic acids in solution and solid state: covalent vs. hydrogen bonding, Phys. Chem. Chem. Phys., 24 (2022), 7882–7892; DOI: 10.1039/d2cp00286h.
  25. M. V. Dobrynin, S. O. Kasatkina, S. V. Baykov, P. Y. Savko, N. S. Antonov, A. S. Mikherdov, V. P. Boyarskiy, R. M. Islamova, Cyclometallated platinum(II) complexes for obtaining phenyl-containing silicone rubbers via catalytic hydrosilylation reaction, Russ. J. Gen. Chem., 92 (2022), 79–84; DOI: 10.1134/S107036322201011X.
  26. K. K. Geyl, S. V. Baykov, S. A. Kalinin, A. S. Bunev, M. A. Troshina, T. V. Sharonova, M. Y. Skripkin, S. O. Kasatkina, S. I. Presnukhina, A. A. Shetnev, M. Y. Krasavin, V. P. Boyarskiy, Synthesis, structure, and antiproliferative action of 2-pyridyl urea-based Cu(II) complexes, Biomedicines, 10 (2022), 461; DOI: 10.3390/biomedicines10020461.
  27. S. Kasatkina, K. Geyl, S. Baykov, M. Novikov, V. Boyarskiy, “Urea to urea” approach: access to unsymmetrical ureas bearing pyridyl substituents, Adv. Synth. Catal., 364 (2022), 1295–1304; DOI: 10.1002/adsc.202101490.
  28. S. V. Baykov, A. V. Semenov, S. I. Presnukhina, A. S. Novikov, A. A. Shetnev, V. P. Boyarskiy. Hydrogen vs. halogen bonding in crystals of 2,5-dibromothiophene-3-carboxylic acid derivatives. J. Mol. Struct., 1260 (2022), 132785; DOI: 10.1016/j.molstruc.2022.132785.
  29. S. V. Baykov, M. V. Tarasenko, A. V. Semenov, E. A. Katlenok, A. A. Shetnev, V. P. Boyarskiy. Dualism of 1,2,4-oxadiazole ring in noncovalent interactions with carboxylic group. J. Mol. Struct., 1262 (2022), 132974; DOI: 10.1016/j.molstruc.2022.132974.
  30. E. Zelenkov, A. A. Eliseeva, S. V. Baykov, D. M. Ivanov, A. I. Sumina, R. M. Gomila, A. Frontera, V. Yu. Kukushkin, N. A. Bokach, Inorganic–organic {dz2-MIIS4}···p-hole stacking in reverse sandwich structures. The case of cocrystals of group 10 metal dithiocarbamates with electron-deficient arenes, Inorg. Chem. Front., 9 (2022) accepted.
  31. I. R. Mardaleishvili, А. В. Вологжанина, А. С. Новиков, A. I. Shienok, L. S. Kol’tsova, N. L. Zaichenko, V. A. Nadtochenko, А. Г. Цховребов, Hydrogen bonding in the crystal of 1,1'-((1E,1'E)-(pyridine-3,4-diylbis(azanylylidene))bis(methanylylidene))-bis(naphthalen-2-ol) acetonitrile solvate: combined experimental and theoretical study, ЖСХ, 63 (2022) 510-512; DOI: 10.26902/JSC_id91711.
  32. I. N. Klyukin, A. V. Kolbunova, A. S. Novikov, A. V. Nelyubin, N. A. Selivanov, A. Y. Bykov, A. A. Klyukina, A. P. Zhdanov, K. Y. Zhizhin, N. T. Kuznetsov, Protonation of borylated carboxonium derivative [2,6-B10H8O2CCH3]−: theoretical and experimental investigation, Int. J. Mol. Sci., 23 (2022) 4190; DOI: 10.3390/ijms23084190.
  33. I. S. Giba, P. M. Tolstoy, V. V. Mulloyarova, A phosphonic acid anion and acid dimer dianion stabilized by proton transfer in OHN hydrogen bonds – models of structural motifs in blend polymer membranes, Phys. Chem. Chem. Phys., 24 (2022) 11362-11369; DOI: 10.1039/D2CP00551D.
  34. A. Pulyalina, K. Grekov, V. Tataurova, A. Senchukova, A. Novikov, I. Faykov, G. Polotskaya, Effect of ionic liquid on formation of copolyimide ultrafiltration membranes with improved rejection of La3+, Sci. Rep., 12 (2022) 8200; DOI: 10.1038/s41598-022-12377-0.
  35. M. V. Grudova, A. S. Novikov, A. S. Kubasov, V. N. Khrustalev, A. A. Kirichuk, V. G. Nenajdenko, A. G. Tskhovrebov, Aurophilic interactions in cationic three-coordinate gold(I) bipyridyl/isocyanide complex, Crystals, 12 (2022) 613; DOI: 10.3390/cryst12050613.
  36. N. A. Korobeynikov, A. N. Usoltsev, T. S. Sukhikh, A. S. Novikov, I. V. Korolkov, V. P. Fedin, M. N. Sokolov, S. A. Adonin, Halogen-rich halorhenates(IV): (Me4N)2{[ReX6](X2)} (X = Cl, Br), Polyhedron, 221 (2022) 115876; DOI: 10.1016/j.poly.2022.115876.
  37. A. Pulyalina, N. Tian, A. Senchukova, I. Faykov, M. Ryabikova, A. Novikov, N. Saprykina, G. Polotskaya, Application of cyclized polyacrylonitrile for ultrafiltration membrane fouling mitigation, Membranes, 12 (2022) 489; DOI: 10.3390/membranes12050489.
  38. N. Y. Shmelev, T. H. Okubazghi, P. A. Abramov, M. I. Rakhmanova, A. S. Novikov, M. N. Sokolov, A. L. Gushchin, Asymmetric coordination mode of phenanthroline-like ligands in gold(I) complexes: a case of the antichelate effect, Cryst. Growth Des., (2022) In press. DOI: 10.1021/acs.cgd.2c00287.
  39. A. A. Artemjev, A. A. Astafiev, A. V. Vologzhanina, A. S. Kubasov, G. M. Burkin, A. S. Novikov, A. S. Kritchenkov, A. A. Kirichuk, A. G. Tskhovrebov, Triarylazoimidazole-ZnII, CdII, and HgII complexes: structures, photophysics, and antibacterial properties, Crystals, 12 (2022) 680; DOI: 10.3390/cryst12050680.
  40. N. A. Korobeynikov, A. N. Usoltsev, P. A. Abramov, A. S. Novikov, M. N. Sokolov, S. A. Adonin, Bromine-rich tin(IV) halide complexes: experimental and theoretical examination of Br···Br noncovalent interactions in crystalline state, Polyhedron, 222 (2022) 115912; DOI: 10.1016/j.poly.2022.115912.
  41. E. A. Katlenok, A. V. Rozhkov, R. R. Ramazanov, R. R. Valiev, O. V. Levin, D. O. Goryachiy, I. V. Taydakov, M. L. Kuznetsov, V. Yu. Kukushkin, Photo- and electroluminescent neutral iridium(III) complexes bearing imidoylamidinate ligands Inorg. Chem., 61 (2022) accepted.
  42. A.S. Novikov, D.S. Bolotin, Хеnon Derivatives as Aerogen Bond-Donating Catalysts for Organic Transformations: A Theoretical Study on the Metaphorical "Spherical Cow in a Vacuum" Provides Insights into Noncovalent Organocatalysis, J. Org. Chem., 2022, in press. DOI: 10.1021/acs.joc.2c00680.
  43. A. S. Novikov, Self-healing polymers, Polymers, 14 (2022) 2261; DOI: 10.3390/polym14112261.
  44. O. S. Taniya, V. V.Fedotov, A. S. Novikov, L. K. Sadieva, A. P. Krinochkin, I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, Y. Liu, E. N. Ulomsky, V. L. Rusinov, V. N. Charushin, Abnormal push-pull benzo[4,5]imidazo[1,2-a][1,2,3]triazolo[4,5-e]pyrimidine fluorophores in planarized intramolecular charge transfer (PLICT) state: Synthesis, photophysical studies and theoretical calculations, Dyes and Pigments, 204 (2022) 110405; DOI: 10.1016/j.dyepig.2022.110405.
  45. P. A. Petrov, E. A. Filippova, T. S. Sukhikh, A. S. Novikov, M. N. Sokolov, Sterically hindered tellurium(IV) catecholate as a Lewis acid, Inorg. Chem., 61 (2022) 9184–9194; DOI: 10.1021/acs.inorgchem.2c00751.
  46. V. А. Rozentsvet, D. M. Ulyanova, N. А. Sablina, M. G. Kuznetsov, P. M. Tolstoy, Polymerization of penta-1,3-diene using cationic catalytic systems based on organoaluminum compounds, Russ. Chem. Bull. 71 (2022) 787-795; DOI: 10.1007/s11172-022-3479-1.
  47. E. Yu. Tupikina, A. A. Titova, M. V. Kaplanskiy, E. R. Chakalov, M. A. Kostin, P. M. Tolstoy, Estimations of OH···N hydrogen bond length from positions and intensities of IR bands, Spectrochim. Acta A 275 (2022), 121172; DOI: 10.1016/j.saa.2022.121172.
  48. M. V. Dobrynin, I. V. Mongilev, A. A. Lezov, I. Perevyazko, P. Tolstoy, Y. A. Anufrikov, A. Yu. Shasherina, P. Vlasov, V. Yu. Kukushkin, R. M. Islamova, Block-copolymeric Maltodextrin-based Amphiphilic Glycosilicones as Surface-active Systems, New J. Chem. 46 (2022) 14849–14858. DOI: 10.1039/D2NJ02285K.
  49. N.A. Shcherbina, I.V. Kazakov, A.S. Lisovenko, M.A. Kryukova, I.S. Krasnova, M.Bodensteiner, A.Y. Timoshkin, Molecular complexes of non-chelating polydentate Lewis bases with group 13 Lewis acids: crystal structure and computed energy of stepwise donor–acceptor bond formation, Mendeleev Comm. 32 (2022), 74-77; DOI: 10.1016/j.mencom.2022.01.024.
  50. V. G. Bardakov, A.A. Yakubenko, V. A. Verkhov, A. S. Antonov, Organoboron Derivatives of 1,8-Bis(dimethylamino)naphthalene: Synthesis, Structure, Stability, and Reactivity, Organometallics, 41 (2022) 1501-1508; DOI: 10.1021/acs.organomet.2c00115.
  51. V. Y. Mikshiev, P. M. Tolstoy, A. M. Puzyk, S. O. Kirichenkoa, A. S. Antonov, peri-Interactions in 1,8-bis(dimethylamino)naphthalene ortho-ketimine cations facilitate [1,5]-hydride shift: selective synthesis of 1,2,3,4-tetrahydrobenzo[h]quinazolines, Org. Biomol. Chem., 20 (2022) 4559-4568; DOI: 10.1039/D2OB00674J.
  52. M.V. Il'in, A.S. Novikov, D.S. Bolotin, Sulfonium and Selenonium Salts as Noncovalent Organocatalysts for the Multicomponent Groebke–Blackburn–Bienaymé Reaction, J. Org. Chem., (2022) in press. DOI: 10.1021/acs.joc.2c01141.
  53. N. V. Shcherbakov, G. D. Titov, E. I. Chikunova, I. Filippov, N. V. Rostovskii, V. Yu. Kukushkin, A. Yu. Dubovtsev, Modular Approach to Non-aromatic and Aromatic Pyrroles through Gold-catalyzed [3+2] Cycloaddition of 2H-Azirines and Ynamides, Org. Chem. Front., (2022), DOI: 10.1039/D2QO01105K.
  54. E.R. Chakalov, E.Yu. Tupikina, D.M. Ivanov, E.V. Bartashevich, P.M. Tolstoy, The Distance between Minima of Electron Density and Electrostatic Potential as a Measure of Halogen Bond Strength, Molecules, 27 (2022) 4848; doi: 10.3390/molecules27154848.
  55. E. Yu. Tupikina, Non-covalent interactions in the glutathione peroxidase active center and their influence on the enzyme activity, Org. Biomol. Chem., 50 (2022); doi: 10.1039/d2ob00890d.
  56. E.Yu. Tupikina, M.V. Sigalov, P.M. Tolstoy, Simultaneous Estimation of Two Coupled Hydrogen Bond Geometries from Pairs of Entangled NMR Parameters: The Test Case of 4-Hydroxypyridine Anion, Molecules, 27 (2022) 3923; doi: 10.3390/molecules27123923.
  57. V. G. Nenajdenko, N. G. Shikhaliyev, A. M. Maharramov, G. T. Atakishiyeva, A. A. Niyazova, N. A. Mammadova, A. S. Novikov, I. V. Buslov, V. N. Khrustalev, A. G. Tskhovrebov, Structural organization of dibromodiazadienes in the crystal and identification of Br···O halogen bonding involving the nitro group, Molecules 27 (2022) 5110; DOI: 10.3390/molecules27165110.
  58. A. A. Muravev, A. S. Ovsyannikov, G. V. Konorov, D. R. Islamov, K. S. Usachev, A. S. Novikov, S. E. Solovieva, I. S. Antipin, Thermodynamic vs. kinetic control in synthesis of O-donor 2,5-substituted furan and 3,5-substituted pyrazole from heteropropargyl precursor, Molecules 27 (2022) 5178; DOI: 10.3390/molecules27165178.
  59. N. A. Korobeynikov, A. N. Usoltsev, A. S. Novikov, P. A. Abramov, M. N. Sokolov, S. A. Adonin, Selenium(IV) polybromide complexes: structural diversity driven by halogen and chalcogen bonding, Molecules 27 (2022) 5355; DOI: 10.3390/molecules27165355.
  60. Y. A. Mezenov, S. Bruyere, A. Krasilin, E. Khrapova, S. V. Bachinin, P. V. Alekseevskiy, S. Shipiloskikh, P. Boulet, S. Hupont, A. Nomine, B. Vigolo, A. S. Novikov, T. Belmonte, V. A. Milichko, Insights into solid-to-solid transformation of MOF amorphous phases, Inorg. Chem. (2022) In press. DOI: 10.1021/acs.inorgchem.2c01978.
  61. N. Kulachenkov, M. Barsukova, P. Alekseevskiy, A. A. Sapianik, M. Sergeev, A. Yankin, A. A. Krasilin, S. Bachinin, S. Shipilovskikh, P. Poturaev, N. Medvedeva, E. Denislamova, P. S. Zelenovskiy, V. V. Shilovskikh, Y. Kenzhebayeva, A. Efimova, A. S. Novikov, A. Lunev, V. P. Fedin, V. A. Milichko, Dimensionality mediated highly repeatable and fast transformation of coordination polymer single crystals for all-optical data processing, Nano Lett. (2022) In press. DOI: 10.1021/acs.nanolett.2c01770.
  62. Ю. Н. Тойкка, А. С. Мерещенко, Г. Л. Старова, Н. А. Бокач, Cинтез, строение и люминесцентные свойства иодидных кластерных комплексов меди(I) с диалкилцианамидными лигандами, Ж. общ. хим., 92 (2022) 1275–1283; DOI: 10.31857/S0044460X22080145.
  63. A. S. Mikherdov, R. A. Popov, A. S. Smirnov, A. A. Eliseeva, A. S. Novikov, V. P. Boyarskiy, R. M. Gomila, A. Frontera, V. Yu. Kukushkin, N. A. Bokach, Isocyanide and сyanide entities form isostructural halogen bond-based supramolecular networks featuring five-center tetrafurcated halogen···C/N bonding, Crystal Growth & Design, 22 (2022); doi: 10.1021/acs.cgd.2c00686.
  64. Y. V. Torubaev, A. V. Rozhkov, I. V. Skabitsky, R. M. Gomila, A. Frontera, V. Yu. Kukushkin, Heterovalent chalcogen bonding. Supramolecular assembly driven by the occurrence of the tellurium(II)···Ch(I) (Ch = S, Se, Te) linkage, Inorg. Chem. Front., 9 (2022); doi: 10.1039/D2QI01420C.
  65. A. Sapegin, E. Rogacheva, L. Kraeva, M. Gureev, M. Dogonadze, T. Vinogradova, P. Yablonsky, S. Balalaie, S. V. Baykov, M. Krasavin, Novel 5-nitrofuran-tagged imidazo-fused azines and azoles amenable by the Groebke–Blackburn–Bienaymé multicomponent reaction: activity profile against ESKAPE pathogens and mycobacteria, Biomedicines, 10 (2022), 2203; DOI: 10.3390/biomedicines10092203.
  66. S. Baykov, M. Tarasenko, V. Kotlyarova, A. Shetnev, L. E. Zelenkov, I. A. Boyarskaya, V. P. Boyarskiy, 2‐(1,2,4‐Oxadiazol‐5‐yl)aniline as a new scaffold for blue luminescent materials, ChemistrySelect, 7 (2022), e202201201; DOI: 10.1002/slct.202201201.
  67. A. Shetnev, M. Tarasenko, V. Kotlyarova, S. Baykov, K. Geyl, S. Kasatkina, N. Sibinčić, V. Sharoyko, E. V. Rogacheva, L. A. Kraeva, External oxidant-free and transition metal-free synthesis of 5-amino-1,2,4-thiadiazoles as promising antibacterials against ESKAPE pathogen strains, Mol. Divers., (2022); DOI: 10.1007/s11030-022-10445-1.
  68. A. S. Nebalueva, A. A. Timralieva, R. V. Sadovnichii, A. S. Novikov, M. V. Zhukov, A. S. Aglikov, A. A. Muravev, T. V. Sviridova, V. P. Boyarskiy, A. L. Kholkin, E. V. Skorb, Piezo-responsive hydrogen-bonded frameworks based on vanillin-barbiturate conjugates, Molecules, 27 (2022), 5659; DOI: 10.3390/molecules27175659.
  69. H. Rajasekaran, P. Jerome, E. V. Eliseenkov, V. P. Boyarskiy, N. Bhuvanesh, R. Karvembu, Half-sandwich Ru(II)-thioamide complexes as catalysts for one pot synthesis of aromatic 1,5-diketones, J. Organomet. Chem., 965–966 (2022), 122322. DOI: 10.1016/j.jorganchem.2022.122322.
  70. E. V. Sokolova, M. A. Kinzhalov, A. S. Smirnov, A. M. Cheranyova, D. M. Ivanov, V. Yu. Kukushkin, N. A. Bokach, Polymorph-dependent phosphorescence of cyclometalated platinum(II) complexes and its relation to non-covalent interactions, ACS Omega, 2022; doi: 10.1021/acsomega.2c04110.
  71. N. K. Neumolotov, N. A. Selivanov, A. Yu. Bykov, I. N. Klyukin, A. S. Novikov, A. P. Zhdanov, K. Yu. Zhizin, N. T. Kuznetsov, New methods for preparation of the monofluorosubstituted derivative of the closo-borate anion [2-B10H9F]2–, its properties, and analysis of its reactivity, Russ. J. Inorg. Chem. 67 (2022) 1583–1590; DOI: 10.1134/S0036023622600861.
  72. V. K. Osmanov, E. V. Chipinsky, V. N. Khrustalev, A. S. Novikov, R. K. Askerov, A. O. Chizhov, G. N. Borisova, A. V. Borisov, M. M. Grishina, M. N. Kurasova, A. A. Kirichuk, A. S. Peregudov, A. S. Kritchenkov, A. G. Tskhovrebov, Facile access to 2-selenoxo-1,2,3,4-tetrahydro-4-quinazolinone scaffolds and corresponding diselenides via cyclization between methyl anthranilate and isoselenocyanates: synthesis and structural features, Molecules 27 (2022) 5799; DOI: 10.3390/molecules27185799.
  73. Y. V. Demyanov, E. H. Sadykov, M. I. Rakhmanova, A. S. Novikov, I. Y. Bagryanskaya, A. V. Artem’ev, Tris(2-pyridyl)arsine as a new platform for design of luminescent Cu(I) and Ag(I) complexes, Molecules 27 (2022) 6059; DOI: 10.3390/molecules27186059.
  74. M. A. Bondarenko, A. S. Novikov, M. N. Sokolov, S. A. Adonin, Heteroleptic Zn(II)–pentaiodobenzoate complexes: structures and features of halogen–halogen non-covalent interactions in solid state, Inorganics 10 (2022) 151; DOI: 10.3390/inorganics10100151.
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  76. A.S. Novikov, D.S. Bolotin, Halonium, Chalconium, and Pnictonium Salts as Noncovalent Organocatalysts: A Computational Study on Relative Catalytic Activity, Org. Biomol. Chem., 2022, DOI: 10.1039/D2OB01415G.
  77. S. V. Baykov, D. M. Ivanov, S. O. Kasatkina, B. Galmés, A. Frontera, G. Resnati, V. Yu. Kukushkin, Stacking interactions: a supramolecular approach to upgrade weak halogen bond donors, Chem. Eur. J., 28 (2022); doi: 10.1002/chem.202201869.
  78. E. I. Chikunova, D. V. Dar’in, V. Yu. Kukushkin, A. Yu. Dubovtsev, Gold-catalyzed oxygen transfer to alkynylsulfones: a benign diazo-free route to 4-sulfonyl-1,3-oxazoles, Adv. Synth. Catal., 2022; doi: 10.1002/adsc.202200751.
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  80. M. A. Bondarenko, M. I. Rakhmanova, A. S. Novikov, M. N. Sokolov, S. A. Adonin, Bi- or trinuclear 2-iodobenzoate complexes of Znii: crystal structures and luminescence, Mendeleev Commun. 32 (2022) 585–587; DOI: 10.1016/j.mencom.2022.09.005.
  81. A. A. Babushkina, V. N. Mikhaylov, A. S. Novikov, V. N. Sorokoumov, M. A. Gureev, M. A. Kryukova, A. O. Shpakov, I. A. Balova, Synthesis, X-ray and DFT studies of 6-halo-3-(hydroxymethyl)cinnolin-4(1H)-ones, Chem. Heterocycl. Comp. 58 (2022) 432–437; DOI: 10.1007/s10593-022-03109-3.
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  83. E. S. Starnovskaya, D. S. Kopchuk, A. F. Khasanov, O. S. Taniya, I. L. Nikonov, M. I. Valieva, D. E. Pavlyuk, A. S. Novikov, G. V. Zyryanov, O. N. Chupakhin, Synthesis and photophysical properties of α-(N-biphenyl)-substituted 2,2′-bipyridine-based push–pull fluorophores, Molecules 27 (2022) 6879; DOI: 10.3390/molecules27206879.
  84. I. N. Klyukin, A. V. Kolbunova, A. S. Novikov, A. P. Zhdanov, K. Y. Zhizhin, N. T. Kuznetsov, Theoretical Insight into B–C Chemical Bonding in Closo-Borate [BnHn−1CH3]2− (n = 6, 10, 12) and Monocarborane [CBnHnCH3]− (n = 5, 9, 11) Anions, Inorganics 10 (2022) 186; DOI: 10.3390/inorganics10110186.
  85. A. V. Nelyubin, I. N. Klyukin, A. S. Novikov, A. P. Zhdanov, N. A. Selivanov, A. Y. Bykov, A. S. Kubasov, K. Y. Zhizhin, N. T. Kuznetsov, New Aspects of the Synthesis of closo-Dodecaborate Nitrilium Derivatives [B12H11NCR]− (R = n-C3H7, i-C3H7, 4-C6H4CH3, 1-C10H7): Experimental and Theoretical Studies, Inorganics 10 (2022) 196; DOI: 10.3390/inorganics10110196.
  86. P. Debnath, P. Debnath, M. Roy, L. Sieroń, W. Maniukiewicz, T. Aktar, D. Maiti, A. S. Novikov, T. K. Misra, Novel Organotin(IV) Complexes of 2-[4-Hydroxy-3-((2-hydroxyethylimino)methyl)phenylazo]benzoic Acid: Synthesis, Structure, Noncovalent Interactions and In Vitro Antibacterial Activity, Crystals 12 (2022) 1582; DOI: 10.3390/cryst12111582.
  87. V. V. Fedotov, M. I. Valieva, O. S. Taniya, S. V. Aminov, M. A. Kharitonov, A. S. Novikov, D. S. Kopchuk, P. A. Slepukhin, G. V. Zyryanov, E. N. Ulomsky, V. L. Rusinov, V. N. Charushin, 4-(Aryl)-Benzo[4,5]imidazo[1,2-a]pyrimidine-3-Carbonitrile-Based Fluorophores: Povarov Reaction-Based Synthesis, Photophysical Studies, and DFT Calculations, Molecules 27 (2022) 8029; DOI: 10.3390/molecules27228029.
  88. E. M. Lorits, E. A. Gubar, A. S. Novikov, Design of the Algorithm for Packaging of Water Molecules in a Fixed Volume, Symmetry 14 (2022) 2453; DOI: 10.3390/sym14112453.
  89. K. K. Geyl, S. V. Baykov, S. O. Kasatkina, P. Yu. Savko, V. P. Boyarskiy, Reaction of coordinated isocyanides with substituted N-(2-pyridyl)ureas as a route to new cyclometallated Pd(II) complexes, J. Organomet. Chem., 980–981 (2022), 122518. DOI: 10.1016/j.jorganchem.2022.122518.
  90. S. I. Presnukhina, M. V. Tarasenko, K. K. Geyl, S. O. Baykova, S. V. Baykov, A. A. Shetnev, V. P. Boyarskiy, Unusual formation of 1,2,4-oxadiazine core in reaction of amidoximes with maleic or fumaric esters, Molecules, 27 (2022), 7508. DOI: 10.3390/molecules27217508.
  91. A. A. Shetnev, A. S. Volobueva, V. A. Panova, V. V. Zarubaev, S. V. Baykov, Design of 4-substituted sulfonamidobenzoic acid derivatives targeting Coxsackievirus B3, Life, 12 (2022), 1832. DOI: 10.3390/life12111832.
  92. D. A. Polonnikov, M. V. Il'in, Ya. V. Safinskaya, I. S. Aliyarova, A. S. Novikov, D. S. Bolotin, (Pre)association as a Crucial Step for Computational Prediction and Analysis of the Catalytic Activity of Sigma-Hole Donating Organocatalysts, Org. Chem. Front., 2022, in press, DOI: 10.1039/D2QO01648F.
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  94. A. S. Novikov, Plethora of non-covalent interactions in coordination and organometallic chemistry are modern smart tool for materials science, catalysis, and drugs design, Int. J. Mol. Sci. 23 (2022) 14767; DOI: 10.3390/ijms232314767.
  95. L. K. Sadieva, I. S. Kovalev, O. S. Taniya, V. A. Platonov, A. S. Novikov, V. S. Berseneva, S. Santra, G. V. Zyryanov, B. C. Ranu, V. N. Charushin, Bola-type PEG-linked polyaromatic hydrocarbon-based chemosensors for the “turn-off” excimer fluorescence detection of nitro-analytes/explosives in aqueous solutions, Dyes and Pigments 210 (2023) 111014; 10.1016/j.dyepig.2022.111014.
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  97. A. S. Miroshnichenko, K. V. Deriabin, A. A. Rashevskii, V. V. Suslonov, A. S. Novikov, I. S. Mukhin, R. M. Islamova, Structural features of Eu3+ and Tb3+-bipyridinedicarboxamide complexes, Polymers 14 (2022) 5540; DOI: 10.3390/polym14245540.
  98. R. A. Popov, A. S. Mikherdov, V. P. Boyarskiy, Pyridine-2(1H)-thione as a bifunctional nucleophile in reaction with PdII and PtII aryl isocyanide complexes. Eur. J. Inorg. Chem., 2022 (2022), e202200217; DOI: 10.1002/ejic.202200217.
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  100. V. Y. Mikshiev, P. M. Tolstoy, E. Yu. Tupikina, A. M. Puzyk, M. A. Vovk, Acid catalysis through N-protonation in undistorted carboxamides: improvement of amide proton sponge acylating ability, New J. Chem. 46 (2022) 16471–16484. DOI: 10.1039/d2nj02975h.
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  104. Strashkov, D.M., Zavyalov, K.V., Sakharov, P.A., ...Khlebnikov, A.F., Novikov, M.S. Rhodium-catalyzed migrative annulation and olefination of 2-aroylpyrroles with diazoesters. Org. Chem. Front. 2022, 10, 506–513. DOI: 10.1039/D2QO01759H.
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