Physical Organic Chemistry
  1. A. V. Rozhkov, E. A. Katlenok, M. V. Zhmykhova, M. L. Kuznetsov, V. N. Khrustalev, K. I. Tugashov, N. A. Bokach, V. Yu. Kukushkin, Spodium bonding to anticrown-Hg3 boosts phosphorescence of cyclometalated-PtII complexes, Inorg. Chem. Front., 10 (2023); 493–510 doi: 10.1039/D2QI02047E.
  2. M. A. Kinzhalov, D. M. Ivanov, A. V. Shishkina, A. A. Melekhova, V. V. Suslonov, A. Frontera, V. Yu. Kukushkin, N. A. Bokach, Halogen bonding between metal-bound I3 and unbound I2: The trapped I2···I3 intermediate in the controlled assembly of copper(I)-based polyiodides, Inorg. Chem. Front., 10 (2023); doi: 10.1039/D2QI02634A.
  3. P.M. Tolstoy, E.Yu. Tupikina, “IR and NMR spectral diagnostics of hydrogen bond energy and geometry” in “Spectroscopy and Computation of Hydrogen-Bonded Systems”, Edited by Marek J. Wojcik, Y. Ozaki, 2023, John Wiley and Sons. pp. 345–407. DOI: 10.1002/9783527834914.ch12.
  4. K. Grzhegorzhevskii, M. Tonkushina, P. Gushchin, I. Gagarin, A. Ermoshin, K. Belova, A. Prokofyeva, A. Ostroushko, A. Novikov, Association of Keplerate-type polyoxometalate {Mo72Fe30} with tetracycline: nature of binding sites and antimicrobial action, Inorganics 11 (2023) 9; DOI: 10.3390/inorganics11010009.
  5. L. Savintseva, A. Avdoshin, S. Ignatov, A. Novikov, Theoretical study of charge mobility in crystal porphine and a computer design of a porphine-based semiconductive discotic liquid mesophase, Int. J. Mol. Sci. 24 (2023) 736; DOI: 10.3390/ijms24010736.
  6. A. Pulyalina, V. Rostovtseva, I. Faykov, N. Saprykina, A. Golikova, A. Fedorova, G. Polotskaya, A. Novikov, Impact of layered perovskite oxide La0.85Yb0.15AlO3 on structure and transport properties of polyetherimide, Int. J. Mol. Sci. 24 (2023) 715; DOI: 10.3390/ijms24010715.
  7. A. S. Novikov, Recent progress in the theoretical studies of the noncovalent interactions of supramolecular complexes with polyhalides and halometalates, Compounds 3 (2023) 27–36; DOI: 10.3390/compounds3010003.
  8. L. G. Lavrenova, A. I. Ivanova, L. A. Glinskaya, A. V. Artem’ev, A. N. Lavrov, A. S. Novikov, P. A. Abramov, Halogen bonding channels for magnetic exchange in Cu(II) complexes with 2,5-di(methylthio)-1,3,4-thiadiazole, Chem. Asian J. (2023) In press. DOI: 10.1002/asia.202201200.
  9. A. S. Smirnov, A. S. Mikherdov, R. M. Gomila, A. Frontera, V. Yu. Kukushkin, N. A. Bokach, Halogen bond-involving supramolecular assembly utilizing carbon as a nucleophilic partner of I···C non-covalent interaction, Chem. Asian J., 2023; doi: 10.1002/asia.202300037.
  10. A. S. Novikov, Non-covalent catalysts, Catalysts 13 (2023), 339; DOI: 10.3390/catal13020339.
  11. A. V. Artem’ev, E. P. Doronina, M. I. Rakhmanova, X. Hei, D. V. Stass, O. A. Tarasova, I. Yu. Bagryanskaya, D. G. Samsonenko, A. S. Novikov, N. A. Nedolya, J. Li, A family of CuI-based 1D polymers showing colorful short-lived TADF and phosphorescence induced by photo- and X-ray irradiation, Dalton Trans. (2023) In press. DOI: 10.1039/D3DT00035D.
  12. I. N. Klyukin, A. V. Kolbunova, A. S. Novikov, A. V. Nelyubin, A. P. Zhdanov, A. S. Kubasov, N. A. Selivanov, A. Y. Bykov, K. Y. Zhizhin, N. T. Kuznetsov, Synthesis of disubstituted carboxonium derivatives of closo-decaborate anion [2,6-B10H8O2CC6H5]−: theoretical and experimental study, Molecules 28 (2023) 1757; DOI: 10.3390/molecules28041757.
  13. E. S. Sheina, T. S. Shestakova, S. L. Deev, I. A. Khalymbadzha, P. A. Slepukhin, O. S. Eltsov, A. S. Novikov, V. A. Shevyrin, V. N. Charushin, O. N. Chupakhin, Mesomeric betaines based on adamantylated 1,2,4-triazolo[4,3-a]pyrimidin-5-ones: synthesis, structure and conversion into anionic N-heterocyclic carbenes, Chem. Asian J. (2023) In press. DOI: 10.1002/asia.202201306.
  14. A. S. Novikov, Recent progress in theoretical studies and computer modeling of non-covalent interactions, Crystals 13 (2023) 361; DOI: 10.3390/cryst13020361.
  15. N. S. Soldatova, V. V. Suslonov, D. M. Ivanov, M. S. Yusubov, G. Resnati, P. S. Postnikov, V. Yu. Kukushkin, Controlled halogen bond-involving assembly of double-σ-hole donating diaryliodonium cations and ditopic arene sulfonates, Crystal Growth & Design, 23 (2023) 413–423; doi: 10.1021/acs.cgd.2c01090.
  16. A. S. Novikov, Theoretical Studies and Computer Modeling of Supramolecular Chemical Systems: Structure, Properties and Reactivity. Chem. Proc. 12 (2022) 88; DOI: 10.3390/ecsoc-26-13717.
  17. K. V. Derkach, M. A. Gureev, A. A. Babushkina, V. N. Mikhaylov, I. O. Zakharova, A. A. Bakhtyukov, V. N. Sorokoumov, A. S. Novikov, M. Krasavin, A. O. Shpakov, I. A. Balova, Dual PTP1B/TC-PTP Inhibitors: Biological Evaluation of 3-(Hydroxymethyl)cinnoline-4(1H)-Ones, Int. J. Mol. Sci. 24 (2023) 4498; DOI: 10.3390/ijms24054498.
  18. A. S. Novikov, Non-Covalent Interactions in Polymers, Polymers 15 (2023) 1139; DOI: 10.3390/polym15051139.
  19. M. A. Bondarenko, D. A. Zherebtsov, A. S. Novikov, V. P. Fedin, S. A. Adonin, Two-dimensional Cu(II) 5-iodoisophthalate with a 1,2-bis(4-pyridyl)ethylene linker: crystal structure and features of electronic structure, J. Struct. Chem. 64 (2023) 112; DOI: 10.1134/S0022476623010079.
  20. I. I. Fedorova, N. S. Soldatova, D. M. Ivanov, K. A. Nikiforova, I. S. Aliyarova, M. S. Yusubov, P. M. Tolstoy, R. M. Gomila, A. Frontera, V. Yu. Kukushkin, P. S. Postnikov, G. Resnati, Benzothienoiodolium cations doubly bonded to anions via halogen-chalcogen and halogen-hydrogen supramolecular synthons, Crystal Growth & Design, 23 (2023); doi: 10.1021/acs.cgd.2c01485.
  21. A. V. Rozhkov, M. V. Zhmykhova, Y. V. Torubaev, E. A. Katlenok, V. Yu. Kukushkin, Bis(perfluoroaryl)chalcolanes ArF2Ch (Ch = S, Se, Te) as σιγμα/πι-hole donors for supramolecular applications based on noncovalent bonding, Crystal Growth & Design, 23 (2023); doi: 10.1021/acs.cgd.2c01454.
  22. A.A. Sysoeva, A.S. Novikov, M.V. Il'in, D.S. Bolotin, Solvent-modulated binding selectivity of reaction substrates to onium-based sigma-hole donors, Catal. Sci. Technol., (2023). DOI: 10.1039/D3CY00071K.
  23. S. A. Katkova, D. O. Kozina, K. S. Kisel, M. A. Sandzhieva, D. A. Tarvanen, S. V. Makarov, V. V. Porsev, S. P. Tunik, M. A. Kinzhalov, Cyclometalated platinum(ii) complexes with acyclic diaminocarbene ligands for OLED application, Dalton Trans., 2023. DOI: 10.1039/d3dt00080j.
  24. A. V. Semenov, S. V. Baykov, N. S. Soldatova, K. K. Geyl, D. M. Ivanov, A. Frontera, V. P. Boyarskiy, P. S. Postnikov, V. Yu. Kukushkin, Noncovalent chelation by halogen bonding in the design of metal-containing arrays: assembly of doubles-hole donating halolium with CuI-containing O,O-donors, Inorg. Chem. , 62 (2023); 10.1021/acs.inorgchem.3c00229.
  25. E. A. Katlenok, N. A. Semenov, M. L. Kuznetsov, N. A. Bokach, V. Yu. Kukushkin, A new look at the chalcogen bond: π-hole-based chalcogen (Se, Te) bonding which does not include a σ-hole interaction, Inorg. Chem. Front., 10 (2023); doi: 10.1039/D3QI00087G.
  26. I. A. Khodov, K. V. Belov, V. V. Sobornova, A. E. Batista de Carvalho Luís, A. A. Dyshin, P. M. Tolstoy, V. V. Mulloyarova, M. G. Kiselev, “Exploring the Conformational Equilibrium of Mefenamic Acid Released from Silica Aerogels via NMR Analysis”, Int. J. Mol. Sci. 24 (2023) 6882; DOI: 10.3390/ijms24086882.
  27. E. Yu. Tupikina, V. O. Korostelev, D. V. Krutin, P. M. Tolstoy, “Evolution of vibrational bands upon gradual protonation/deprotonation of arsinic acid H2AsOOH in media of different polarity”, Phys. Chem. Chem. Phys. 25 (2023) 8664-8675; DOI: 10.1039/D2CP06060D.
  28. U. M. Leksina, A. Y. Shishov, V. V. Mulloyarova, A. M. Puzyk, P. M. Tolstoy, M. Vokuev, E. D. Glushkov, V. G. Petrov, P. I. Matveev, “A new deep eutectic solvent based on diphenylguanidine for the effective extraction of pertechnetate anion”, Sep. Purif. Technol. (2023), available online; DOI: 10.1016/j.seppur.2023.123824.
  29. Y. S. Bortnevskaya, N. A. Shiryaev, N. S. Zakharov, O. O. Kitoroage, M. A. Gradova, N. Y. Karpechenko, A. S. Novikov, E. D. Nikolskaya, M. R. Mollaeva, N. G. Yabbarov, N. A. Bragina, K. A. Zhdanova, Synthesis and Biological Properties of EGFR-Targeted Photosensitizer Based on Cationic Porphyrin, Pharmaceutics 15 (2023) 1284; DOI:10.3390/pharmaceutics15041284.
  30. I. F. Sakhapov, A. A. Zagidullin, A. B. Dobrynin, I. A. Litvinov, D. G. Yakhvarov, M. A. Bondarenko, A. S. Novikov, V. P. Fedin, S. A. Adonin, Crystal Structures of 3,3′,5,5′-Tetrabromo-4,4′-bipyridine and Co(II) Coordination Polymer Based Thereon, Crystals 13 (2023) 704; DOI: 10.3390/cryst13040704.
  31. A. A. Eliseeva, M. A. Khazanova, A. M. Cheranyova, I. A. Aliyarova, R. I. Kravchuk, E. S. Oganesyan, A. V. Ryabykh, O. A. Maslova, D. M. Ivanov, S. A. Beznosyuk, Metal-involving halogen bonding confirmed using DFT calculations with periodic boundary conditions, Crystals, 13 (2023), 712; DOI: 10.3390/cryst13050712.
  32. E. V. Podrezova, A. A. Okhina, A. D. Rogachev, S. V. Baykov, A. Kirschning, M. S. Yusubov, N. S. Soldatova, P. S. Postnikov, Ligand-free Ullmann-type arylation of oxazolidinones by diaryliodonium salts. Org. Biomol. Chem., 21 (2023), 1952–1957; DOI: 10.1039/D2OB02122F.
  33. E. O. Sinegubova, O. A. Kraevaya, A. S. Volobueva, A. V. Zhilenkov, A. F. Shestakov, S. V. Baykov, S. V. P. A. Troshin, V. V. Zarubaev, Water-Soluble Fullerene C60 Derivatives Are Effective Inhibitors of Influenza Virus Replication. Microorganisms, 11 (2023), 681; DOI: 10.3390/microorganisms11030681.
  34. S. V. Baykov, A. A. Shetnev, A. V. Semenov, S. O. Baykova, V. P. Boyarskiy, Room Temperature Synthesis of Bioactive 1,2,4-Oxadiazoles. Int. J. Mol. Sci., 24 (2023), 5406; DOI: 10.3390/ijms24065406.
  35. A. Shetnev, A. Kotov, A. Kunichkina, I. Proskurina, S. Baykov, M. Korsakov, A. Petzer, J. P. Petzer, Monoamine Oxidase Inhibition Properties of 2,1-Benzisoxazole Derivatives. Mol. Divers. (2023); DOI: 10.1007/s11030-023-10628-4.
  36. K. V. Deriabin, E. A. Golovenko, N. Antonov, S. Baykov, V. Boyarskiy, R. M. Islamova, Platinum-Macrocatalyst for Heterogeneous Si–O Dehydrocoupling. Dalt. Trans. (2023), in press; DOI: 10.1039/D3DT00651D.
  37. Baykova, S. O.; Geyl, K. K.; Baykov, S. V.; Boyarskiy, V. P. Synthesis of 3-(Pyridin-2-Yl)Quinazolin-2,4(1H,3H)-Diones via Annulation of Anthranilic Esters with N-Pyridyl Ureas. Int. J. Mol. Sci., 24 (2023), 7633; DOI: 10.3390/ijms24087633.
  38. I.N. Klyukin, A.V. Kolbunova, A.S. Novikov, A.P. Zhdanov, K.Y. Zhizhin, N.T. Kuznetsov, Theoretical Insight on the Formation Mechanism of a Trisubstituted Derivative of Closo-Decaborate Anion [B10H7O2CCH3(NCCH3)]0, Inorganics 11 (2023) 201; DOI: 10.3390/inorganics11050201.
  39. I.S. Fomenko, O.S. Koshcheeva, N.I. Kuznetsova, T.V. Larina, M.I. Gongola, M. Afewerki, P.A. Abramov, A.S. Novikov, A.L. Gushchin, Novel Copper(II) Complexes with BIAN Ligands: Synthesis, Structure and Catalytic Properties of the Oxidation of Isopropylbenzene, Catalysts 13 (2023) 849; DOI: 10.3390/catal13050849.
  40. D.S. Suslov, M.V. Bykov, M.V. Pakhomova, T.S. Orlov, Z.D. Abramov, A.V. Suchkova, I.A. Ushakov, P.A. Abramov, A.S. Novikov, Novel Route to Cationic Palladium(II)–Cyclopentadienyl Complexes Containing Phosphine Ligands and Their Catalytic Activities, Molecules 28 (2023) 4141; DOI: 10.3390/molecules28104141.
  41. E.S. Starnovskaya, M.I. Savchuk, R. Aluru, D.S. Kopchuk, A.F. Khasanov, O.S. Taniya, A.S. Novikov, A.A. Kalinichev, S. Santra, G.V. Zyryanov, B.C. Ranu, Carbazole/fluorene substituted 5-phenyl-2,2'-bipyridine D-π-A fluorophores: Photophysical data, hyperpolarizability and CT-indices, New J. Chem. (2023) In press.; DOI: 10.1039/D3NJ00394A.
  42. M.R. Guda, M.I. Valieva, D.S. Kopchuk, R. Aluru, A.F. Khasanov, O.S. Taniya, A.S. Novikov, G.V. Zyryanov, B. C. Ranu, One-pot synthesis and photophysical studies of Α-cycloamino-substituted 5-aryl-2,2'-bipyridines, J. Fluoresc. (2023) In press.; DOI: 10.1007/s10895-023-03304-1.
  43. M.S. Mohammed, I.S. Kovalev, N.V. Slovesnova, L.K. Sadieva, V.A.Platonov, A.S. Novikov, S. Santra, J.E. Morozova, G.V. Zyryanov, V.N. Charushin, B.C. Ranu, Polyaromatic hydrocarbon (PAH)-based aza-POPOPs: synthesis, photophysical studies, and nitroanalyte sensing abilities, Int. J. Mol. Sci. 24 (2023) 10084; DOI: 10.3390/ijms241210084.
  44. R.A. Popov, A.S. Novikov, V.V. Suslonov, V.P. Boyarskiy, Molecular switching through chalcogen-bond-induced isomerization of binuclear (diaminocarbene)PdII complexes, Inorganics 11 (2023) 255; DOI: 10.3390/inorganics11060255.
  45. I.A. Shentseva, N.A. Korobeynikov, A.N. Usoltsev, I.D. Gorokh, A.S. Novikov, I.V. Korolkov, M.N. Sokolov, S.A. Adonin, Haloantimonate(III) complexes with halogen-substituted quinolinium cations: structural features of non-covalent interactions in solid state, Polyhedron (2023) In press.; DOI: 10.1016/j.poly.2023.116505.
  46. N.F. Romashev, I.V. Bakaev, V.I. Komlyagina, P.A. Abramov, I.V. Mirzaeva, V.A. Nadolinny, A.N. Lavrov, N.B. Kompan’kov, A.A. Mikhailov, I.S. Fomenko, A.S. Novikov, M.N. Sokolov, A.L. Gushchin, Iridium complexes with BIAN-type ligands: synthesis, structure and redox chemistry, Int. J. Mol. Sci. 24 (2023) 10457; DOI: 10.3390/ijms241310457.
  47. M. V. Kashina, M. A. Kinzhalov, E. Yu. Tupikina, V. Yu. Kukushkin, Bent and linear noncovalent M···S=C=N–M’ interactions. The case of palladium(II) and platinum(II) thiocyanate species, Crystal Growth & Design, 23 (2023); doi:10.1021/acs.cgd.3c00116.
  48. E. A. Katlenok, M. L. Kuznetsov, A. V. Cherkasov, D. M. Kryukov, N. A. Bokach, V. Yu. Kukushkin, Metal-involved C···dz2-PtII tetrel bonding as a principal component of the stacking interaction between arenes and the platinum(II) square-plane, Inorg. Chem. Front., 10 (2023); doi: 10.1039/D3QI00555K.
  49. Yu. N. Toikka, G. L. Starova, V. V. Suslonov, R. M. Gomila, A. Frontera, V. Yu. Kukushkin, N. A. Bokach, Combined sigma- and pi-hole donor properties of perfluorinated iodo(or bromo)benzenes: halogen bonding and pi-hole interactions in cocrystals including Cu4I4 clusters, Crystal Growth & Design, 23 (2023); doi: 10.1021/acs.cgd.3c00412.
  50. N. V. Shcherbakov, P. F. Kotikova, D. V. Dar’in, V. Yu. Kukushkin, A. Yu. Dubovtsev, Gold-catalyzed annulation of ynamides with aminocarbonyls as a route to 2-aminoquinolines diversely substituted at the 4th-position, Adv. Synth. Catal., 365 (2023); doi: 10.1002/adsc.202300484.
  51. A.A. Peshkov, D. Gapanenok, A. Puzyk, N. Amire, A.S. Novikov, S.D. Martynova, S. Kalinin, D. Dar’in, V.A. Peshkov, M. Krasavin, Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles, J. Org. Chem. (2023) In press. DOI: 10.1021/acs.joc.3c00497.
  52. M.S. Mohammed, I.S. Kovalev, N.V. Slovesnova, L.K. Sadieva, V.A. Platonov, G.A. Kim, R. Aluru, A.S. Novikov, O.S. Taniya, V.N. Charushin, (1-(4-(5-Phenyl-1,3,4-oxadiazol-2-yl)phenyl)-1H-1,2,3-triazol-4-yl)-methylenyls α,ω-Bisfunctionalized 3- and 4-PEG: Synthesis and Photophysical Studies, Molecules 28 (2023) 5256; DOI: 10.3390/molecules28135256.
  53. E.A. Lystsova, A.S. Novikov, M.V. Dmitriev, A.N. Maslivets, E.E. Khramtsova, Approach to Pyrido[2,1-b][1,3]benzothiazol-1-ones via In Situ Generation of Acyl(1,3-benzothiazol-2-yl)ketenes by Thermolysis of Pyrrolo[2,1-c][1,4]benzothiazine-1,2,4-triones, Molecules 28 (2023) 5495; DOI: 10.3390/molecules28145495.
  54. A. S. Smirnov, M. A. Kinzhalov, R. M. Gomila, A. Frontera, N. A. Bokach, V. Yu. Kukushkin, Isocyanide π-hole interactions supported by aurophilic forces, Crystals, 13 (2023) 1177; doi: 10.3390/cryst13081177.
  55. A. D. Radzhabov, N. S. Soldatova, D. M. Ivanov, M. S. Yusubov, V. Yu. Kukushkin, P. S. Postnikov, Metal-free and atom-efficient protocol for diarylation of selenocyanate by diaryliodonium salts, Org. Biomol. Chem., 21 (2023); doi: 10.1039/D3OB00833A.
  56. N. A. Zhestkij, A. S. Efimova, Y. Kenzhebayeva, M. V. Dmitriev, A. S. Novikov, I. D. Yushina, A. Krylov, M. V. Timofeeva, A. N. Kulakova, N. V. Glebova, A. A. Krasilin, S. A. Shipilovskih, V. A. Milichko, Nonlinear Metal–Organic Framework Crystals for Efficient Multicolor Coherent Optical Emission, Adv. Optical Mater. (2023) In press. DOI: 10.1002/adom.202300881.
  57. A. S. Novikov, Symmetry in Quantum and Computational Chemistry: Volume 2, Symmetry 15 (2023) 1472; DOI: 10.3390/sym15081472.
  58. E. E. Bardina, E. V. Makotchenko, K. P. Birin, I. A. Baidina, T. S. Sukhikh, A. S. Novikov, Y. G. Gorbunova, A. Yu. Tsivadze, A. L. Gushchin, Noncovalent interactions in gold(III) tetrakis(4-butoxyphenyl)porphyrinate structures, CrystEngComm (2023) In press. DOI: 10.1039/D3CE00428G.
  59. M. Shahab, G. Zheng, A. Khan, D. Wei, A. S. Novikov, Machine Learning-Based Virtual Screening and Molecular Simulation Approaches Identified Novel Potential Inhibitors for Cancer Therapy, Biomedicines 11 (2023) 2251; DOI: 10.3390/biomedicines11082251.
  60. V. G. Nenajdenko, A. A. Kazakova, A. S. Novikov, N. G. Shikhaliyev, A. M. Maharramov, A. M. Qajar, G. T. Atakishiyeva, A. A. Niyazova, V. N. Khrustalev, A. V. Shastin, A. G. Tskhovrebov, Copper-Catalyzed Reaction of N-Monosubstituted Hydrazones with CBr4: Unexpected Fragmentation and Mechanistic Study, Catalysts 13 (2023) 1194; DOI: 10.3390/catal13081194.
  61. A. Dogaru, A. A. Apostol, C. Maxim, M. Raduca, A. S. Novikov, A. Nicolescu, C. Deleanu, S. Nica, M. Andruh, Halogen bonded supramolecular assemblies constructed from azulene derivatives and perfluorinated di-/triiodobenzenes, CrystEngComm (2023) In press. DOI: 10.1039/D3CE00752A.
  62. A. S. Smirnov, E. A. Katlenok, A. S. Mikherdov, M. A. Kryukova, N. A. Bokach, V. Yu. Kukushkin, Halogen bonding involving isomeric isocyanide/nitrile groups, Int. J. Mol. Sci., 24 (2023) 13324; doi: 10.3390/ijms241713324.
  63. N. A. Korobeynikov, A. N. Usoltsev, M. N. Sokolov, A. S. Novikov, T. S. Sukhikh, S. A. Adonin, Halogen bonding in chloroiodates(III), CrystEngComm (2023) In press. DOI: 10.1039/D3CE00400G.
  64. A. S. Novikov, Computer Modeling and Machine Learning in Chemistry and Materials Science: From Properties and Reactions of Small Organic and Inorganic Molecules to the Smart Design of Polymers and Composites, Compounds 3 (2023) 459; DOI: 10.3390/compounds3030034.
  65. Agafonova A. V., Golubev A. A., Smetanin I. A., Khlebnikov A. F., Spiridonova D. V., Novikov M. S. Divergent Synthesis of Pyrazolo[1,5-a]pyridines and Imidazo[1,5-a]pyridines via Reagent-Controlled Cleavage of the C–N or C–C Azirine Bond in 2-Pyridylazirines. Org. Lett. 2023, DOI: 10.1021/acs.orglett.3c02696.
  66. Mammeri O. A., Baranov I. M., Ivanov A. Yu., Boyarskaya I. A., Vasilyev A. V. Synthesis of 2-(5H)-furanones by cyclization of alkyl allene carboxylates in triflic acid. Tetrahedron 2023, 146, 133649. DOI: 10.1016/j.tet.2023.133649
  67. Il’in, M.V., Polonnikov, D.A., Novikov, A.S., Sysoeva, A.A., Safinskaya, Y.V., Bolotin, D.S. Influence of Coordination to Silver(I) Centers on the Activity of Heterocyclic Iodonium Salts Serving as Halogen-Bond-Donating Catalysts. ChemPlusChem 2023, e202300304. DOI: 10.1002/cplu.202300304.
  68. Pankova, A.S., Golubev, P., Molin, I.A., Rostovskii, N.V. Regioselective Synthesis of 2-Trimethylsilyl-4H-pyran-4-ones from 1-Ethoxy(hydroxy)-5-(trimethylsilyl)pentenynones. Eur. J. Org. Chem. 2023, 26, e202300573. DOI: 10.1002/ejoc.202300573.
  69. Vidyakina, A.A., Shtyrov, A.A., Ryazantsev, M.N., Khlebnikov, A. F., Kolesnikov, I. E., Sharoyko, V. V., Spiridonova, D. V., Balova, I. A., Bräse, S., Danilkina, N.A. Development of Fluorescent Isocoumarin-Fused Oxacyclononyne – 1,2,3-Triazole Pairs. Chem. Eur. J. 2023, 29, e202300540. DOI: 10.1002/chem.202300540.
  70. Galenko, E.E., Novikov, M.S., Khlebnikov, A.F. [2+2] Cycloaddition/Retro-Electrocyclization/Decarboxylation Reaction Sequence: Access to 4-Aminopyridines from Methylideneisoxazolones and Ynamines. J. Org. Chem. 2023, 88, 8854–8864. DOI: 10.1021/acs.joc.3c00654.
  71. Silaichev, P.S., Beryozkina, T.V., Ilkin, V., Novikov, M.S., Dehaen, W., Bakulev, V.A. Tandem Cycloaddition of Azides to 3,3-Diaminoacrylonitriles (2-Cyanoacetamidines) and Cornforth-Type Rearrangement as an Approach to 5-Amino-1,2,3-triazole-4-N-substituted Imidamides. J. Org. Chem. 2023, 88, 8163–8174. DOI: 10.1021/acs.joc.3c00151.
  72. Vasilchenko, D.S., Agafonova, A.V., Simdianov, I.V., Koronatov, A. N., Sakharov, P.A., Romanenko, I. A., Rostovskii, N.V., Khlebnikov, A.F., Novikov, M.S. 2H-1,2,3-triazole-4-carboxylic acids via Ru(II)-catalyzed rearrangement of 4-hydrazonoisoxazol-5-ones. Tetrahedron Lett. 2023, 123, 154580. DOI: 10.1016/j.tetlet.2023.154580.
  73. Zakharov, T.N., Sakharov, P.A., Novikov, M.S., Khlebnikov, A.F., Rostovskii, N.V. Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study. Molecules 2023, 28, 4315. DOI: 10.3390/molecules28114315.
  74. Taishev, A.E., Galenko, E.E., Novikov, M.S., Khlebnikov, A.F. Simple Access to Isoxazole-Containing Heterocyclic Hybrids: Isoxazole/Oxazole and Isoxazole/Pyridine. Russ. J. Gen. Chem. 2023, 93, 1246–1260. DOI: 10.1134/s1070363223050250.
  75. Titov, G.D., Antonychev, G.I., Novikov, M.S., Khlebnikov, A.F., Rogacheva, E. V., Kraeva, L.A., Rostovskii, N.V. Gold vs Light: Chemodivergent Reactivity of Diazoesters toward 2H-Azirine-2-carboxylic Acids. Org. Lett. 2023, 25, 2707–2712. DOI: 10.1021/acs.orglett.3c00823.
  76. Galenko, E.E., Zanakhov, T.O., Novikov, M.S., Khlebnikov, A.F. Metal carbonyl mediated rearrangement of 5-(2-oxoalkyl)-1,2,4-oxadiazoles: synthesis of fully substituted pyrimidines. Org. Biomol. Chem. 2023, 21, 2990–3001. DOI: 10.1039/D3OB00148B.
  77. Galenko, E.E., Zanakhov, T.O., Novikov, M.S., Khlebnikov, A.F. Pd-catalyzed heteroannulation of isoxazoles: Convergent synthesis of isoxazolo[5,4-c]quinolones. Tetrahedron Lett. 2023, 114, 154270. DOI: 10.1016/j.tetlet.2022.154270.
  78. Agafonova, A.V., Novikov, M.S., Khlebnikov, A.F. 5-Chloroisoxazoles: A Versatile Starting Material for the Preparation of Amides, Anhydrides, Esters, and Thioesters of 2H-Azirine-2-carboxylic Acids. Molecules 2023, 28, 275. DOI: 10.3390/molecules28010275.
  79. Govdi, A.I., Anisimov, S.O., Danilkina, N.A., Bunev, A.S., Balova, I.A. Acyclic enediynes fused to triazole and benzothiophene containing propargylamine moieties. Mendeleev Commun. 2023, 33, 328–330. DOI: 10.1016/j.mencom.2023.04.010.
  80. Babushkina, A.A., Mikhailov, V.N., Ogurtsova, A.D., Bunev, A. S., Sorokoumov, V.N., Balova, I.A. The Richter reaction in the synthesis of combretastatin analogs. Russ. Chem. Bull. 2023, 72, 1012–1022. DOI: 10.1007/s11172-023-3866-3.
  81. Derkach, K.V., Gureev, M.A., Babushkina, A.A., Mikhaylov, V.N., Zakharova, I.O., Bakhtyukov, A.A., Sorokoumov, V.N., Novikov, A.S., Krasavin, M., Shpakov, A.O., Balova, I.A. Dual PTP1B/TC-PTP Inhibitors: Biological Evaluation of 3-(Hydroxymethyl)cinnoline-4(1H)-Ones. Int. J. Mol. Sci. 2023, 24, 4498. DOI: 10.3390/ijms24054498.
  82. Efremova, M.M., Rumyantsev, A.M., Babitova, E.S., Ianshina, T.M., Govdi, A.I. Synthesis of 5-ethynylisoxazoles based on 1,3-dipolar cycloaddition reactions of nitrile oxides with conjugated diynes. Russ. Chem. Bull. 2023, 72, 1717–1721. DOI: 10.1007/s11172-023-3952-5.
  83. Cells Ianshina, T., Sidorin, A., Petrova, K., Shubert, M., Makeeva, A., Sambuk, E., Govdi, A., Rumyantsev, A., Padkina, M. Effect of Methionine on Gene Expression in Komagataella phaffii. Microorganisms 2023, 11, 877. DOI: 10.3390/microorganisms11040877.
  84. Sokolov, A.A., Egorov, D.M., Pronina, Y.A., Ramsh, S.M., Stepakov, A.V. 1,3-Dipolar Cycloaddition of Stable Azomethine Ylide Based on Ninhydrin and L-Proline to Phosphorylated Acetylenes. Russ. J. Gen. Chem. 2023, 93, 1694–1699. DOI: 10.1134/S1070363223070083
  85. Pevzner, L.M., Makhneva, E.A., Shmakov, S.V., Petrov, M.L., Stepakov, A.V., Boitsov, V.M. In Vitro Activity of Organochalcogen Compounds: IV. Synthesis and Cytotoxic Effect of 4-(1,2,3-Thiadiazol-4-yl)furans Against HeLa, Sk-mel-2, and B16 Tumor Cell Lines. Russ. J. Gen. Chem. 2023, 93, 1513–1522. DOI: 10.1134/S1070363223060245.
  86. Pevzner, L.M., Ostrovskaya, A.A., Petrov, M.L., Stepakov, A.V. Synthesis of Ethyl 2-Methyl-4-(diethoxyphosphoryl)-4,7-dihydro-5H-thiopyrano[3,4-b]furan-5-carboxylate and Its Functionalization at the Position 3. Russ. J. Gen. Chem. 2023, 93, 827–840. DOI: 10.1134/S1070363223040084.
  87. Pronina, Y.A., Stepakov, A.V., Popova, E.A., Boitsov, V.M., Baichurin, R.I., Selivanov, S.I. Diastereomers of Cyclopropa[a]pyrrolizine Spiro-fused with a Benzo[4,5]imidazo[1,2-a]indole Fragment: Structure Determinations Using NMR Methods. Appl. Magn. Reson. 2023 DOI: 10.1007/s00723-023-01608-w.
  88. Komolova, D.D., Pronina, Y.A., Lozovskiy, S.V., Selivanov, S.I., Ponyaev, A.I., Filatov, A.S., Boitsov, V.M., Stepakov, A.V. Palladium-Catalyzed Oxidative Cycloaddition of Quinazoline-2,4(1H,3H)-diones and Diarylalkynes via C-H/N-H Activation. Synthesis 2023 DOI: 10.1055/a-2105-2850.
  89. Makeeva, D.V., Antipova, K.S., Solovyeva, E.V., Morgacheva, V.P., Kolobova, E.A., Kartsova, L.A. Multilayer Coatings Based On Citrate-Stabilized Gold Nanoparticles and Polydiallyldimethylammonium Chloride for the Electrophoretic Separation of Carboxylic Acids. J. Anal. Chem. 2023, 78, 361–371. DOI: 10.1134/S1061934823030085.
  90. Kartsova, L.A., Maliushevska, A.V., Kolobova, E.A. Analytical Capabilities of the Determination of Carbohydrates by Chromatographic and Electrophoretic Methods. J. Anal. Chem. 2023, 78, 144–161. DOI: 10.1134/S1061934823020041.
  91. Karpitskiy, D.A., Bessonova, E.A., Shishov, A.Y., Kartsova, L.A. Selective extraction of plant bioactive compounds with deep eutectic solvents: Iris sibirica L. as example. Phytochem. Anal. 2023 DOI: 10.1002/pca.3272.
  92. Kravchenko, A.V., Kolobova, E.A., Kechin, A.A., Kartsova, L.A. Development of a capillary electrophoretic method for determination of ketorolac enantiomers in human plasma using cationic β-cyclodextrin derivative as a chiral selector. J. Sep. Sci. 2023, 46, 2200601. DOI: 10.1002/jssc.202200601.
  93. Zakusilo, D.N., Evstigneyev, E.I., Ivanov, A.Y., Mazur, A.S., Bessonova, E.A., Mammeri, O.A., Vasilyev, A.V. Structure of oxidized hydrolysis lignin. J. Wood Chem. Technol. 2023, 43, 103–115. DOI: 10.1080/02773813.2023.2187064.
  94. Zenkevich, I.G. Linear Correlations of the Gas Chromatographic Retention Indices of Compounds from Various Taxonomic Groups. J. Anal. Chem. 2023, 78, 766–775. DOI: 10.1134/S1061934823040160.
  95. Zenkevich, I.G., Deruish, A., Nikitina, D.A. Features of the Dependence of the Retention Indices of Sorbates in Reversed-Phase High-Performance Liquid Chromatography on the Content of Organic Solvents in the Eluent. Russ. J. Phys. Chem. A 2023, 97, 1007–1017. DOI: 10.1134/S0036024423050321.
  96. Deruish, A., Karakashev, G.V., Ukolov, A.I., Zenkevich, I.G. Hydrolytic Stability of Unsubstituted Hydrazones of Aromatic Carbonyl Compounds in Reversed-Phase HPLC. J. Anal. Chem. 2023, 78, 222–230. DOI: 10.1134/S106193482302003X.
  97. Savina, I.A., Gusev, D.M., Zimina, T.V., Golovanov, A.A., Zenkevich, I.G. Comparison of Gas-Chromatographic Retention Parameters of Aliphatic Enyne Alcohols with the Data for Their Structural Analogues. J. Anal. Chem. 2023, 78, 74–81. DOI: 10.1134/s1061934822120139.
  98. Zenkevich, I.G., Baranov, D.A. Gas-Chromatographic Identification of Unusual Unstable Products of the Partial Hydrolysis of Tetraethoxysilane. J. Anal. Chem. 2023, 78, 82–90. DOI: 10.1134/S1061934823010148.
  99. Zenkevich, I.G., Derouiche, A., Nikitina, D.A. Evidence for the Hydration of Some Organic Compounds during Reverse-Phase HPLC Analysis. Molecules 2023, 28, 734. DOI: 10.3390/molecules28020734.
  100. Ignatova, I.I., Khoroshilova, O.V., Vasilyev, A.V. Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. Mendeleev Commun. 2023, 33, 27–29. DOI: 10.1016/j.mencom.2023.01.008.
  101. Samandarsangari, M., Kozina, D.O., Sokolov, V.V., Komarova, A.D., Shirmanova, M.V., Kritchenkov, I.S., Tunik, S.P. Biocompatible Phosphorescent O2 Sensors Based on Ir(III) Complexes for In Vivo Hypoxia Imaging. Biosensors 2023, 13, 680. DOI: 10.3390/bios13070680.
  102. Novichikhina, N.P., Pantykina, D.A., Shestakov, A.S., Potapov, A.Yu., Ledenyova, I.V., Kuznetsov, M.A., Shikhaliev, K.S. Allylic and Retro-Allylic Rearrangements upon Bromination of 8,9-Substituted 4,4,6-Trimethyl-4H-Pyrrolo[3,2,1-ij]Quinoline-1,2-Diones. New Aspects and Synthetic Applications. ChemistrySelect 2023, 8, e202203981. DOI: 10.1002/slct.202203981.
  103. Solovyeva, E.V., Odintsova, O.V., Svinko, V.O., Makeeva, D.V., Danilov, D.V. Hydroxyapatite-nanosilver composites with plasmonic properties for application in surface-enhanced Raman spectroscopy. Mater. Today Commun. 2023, 35, 105908. DOI: 10.1016/j.mtcomm.2023.105908.
  104. P. Debnath, P. Debnath, S. Roy, M. B. Devi, M. M. Devi, K. Sarangthem, S. S. Singh, M. Roy, A. S. Novikov, T. K. Misra, Azo-benzoic acid derivatives directed dinuclear and tetranuclear association of trimethyltin(IV) complex components and their biological activities, Inorg. Chim. Acta 559 (2024) 121805; DOI: 10.1016/j.ica.2023.121805.
  105. W.K.A. Al-Ithawi, R. Aluru, A.V. Baklykov, A.F. Khasanov, I.S. Kovalev, I.L. Nikonov, D.S. Kopchuk, A.S. Novikov, S. Santra, G.V. Zyryanov, B.C. Ranu, Mechanosynthesis of Polyureas and Studies of Their Responses to Anions, Polymers 15 (2023) 4160; DOI: 10.3390/polym15204160.
  106. K.A. Zhdanova, A.A. Zaytsev, M.A. Gradova, O.V. Gradov, A.V. Lobanov, A.S. Novikov, N.A. Bragina, Synthesis, Photophysical Properties, and Toxicity of o-Xylene-Bridged Porphyrin Dimers, Inorganics 11 (2023) 415; DOI: 10.3390/inorganics11100415.
  107. V. A. Rozentsvet, D. M. Ulyanova, N. A. Sablina, R. V. Brunilin, P. M. Tolstoy, Synthesis of Low Molecular Weight Butadiene Polymers Using Cationic Catalytic Systems Based on Diethylaluminum Chloride, Kinetics and Catalysis 64 (2023) 55; DOI: 10.1134/S0023158423010068.
  108. K. Sotiriadis, A. Mazur, P. Tolstoy, R. Ševčík, Exposure of Portland-Limestone Cement – Metakaolin Paste to Cold Chloride-Sulfate Environment: NMR Spectroscopy Assessment of Structural Changes in Hydrated Phases and Relation to Chloride Ingress, RILEM Bookseries 44 (2023) 966; DOI: 10.1007/978-3-031-33187-9_88.
  109. V. А. Rozentsvet, D. M. Ulyanova, N. А. Sablina, P. M. Tolstoy, M. G. Kuznetsov, Cationic polymerization of butadiene with isomerization of the initiator structure, Russ. Chem. Bull. 72 (2023) 2180; DOI: 10.1007/s11172-023-4014-8.
  110. V. A. Rozentsvet, D. M. Ulyanova, N.A. Sablina, S. V. Kostjuk, N. V. Sidorenko, P. M. Tolstoy, Diethylaluminum chloride-co-initiated cationic polymerization of isoprene: dramatic effect of the nature of alkyl halide on the properties of synthesized polymers, J. Macromol. Sci. A 60 (2023) 705; DOI: 10.1080/10601325.2023.2257739.
  111. K. Sotiriadis, A. Mazur, P. M. Tolstoy, D. Frankeova, Chloride effect on sulfate attack in hydrated Portland-limestone cement assessed by 29Si NMR spectroscopy and thermal analysis, Mater. Today: Proc. (2023) in press; DOI: 10.1016/j.matpr.2023.06.185.
  112. E. R. Chakalov, R. P. Shekurov, V. A. Miluykov, P. M. Tolstoy, Evidence of extremely short hydrogen bond in homoconjugated anion of ferrocene-1,1’-diyl-bisphosphinic acid: sign change of H/D isotope effect on the 31P NMR chemical shift, Phys. Chem. Chem. Phys. (2023) in press; DOI: 10.1039/D3CP03714B.
  113. E.S. Starnovskaya, M.I. Savchuk, D.S. Kopchuk, O.S. Taniya, A.F. Khasanov, A.S. Novikov, N.V. Slovesnova, A.S. Minin, S. Santra, G.V. Zyryanov, 2-(Indol-3-yl)- and 6-(pyrrol-2-yl)-substituted (bi)pyridine-based AIE-probes/fluorophores: Synthesis and photophysical studies, New J. Chem. (2023) In press.; DOI: 10.1039/D3NJ04051H.
  114. S. Roy, S. Mal, R. Banik, S. Das, Ľ. Dlháň, J. Titiš, R. Boča, A.M. Kirillov, A.S. Novikov, P. Hazendonk, R.J. Butcher, A. Bauza, A. Frontera, Two isostructural complexes of Ni(II) and Zn(II) with violurate and pyridine: a detailed structural, theoretical, magnetic, and NMR investigation, CrystEngComm (2023) In press.; DOI: 10.1039/d3ce00871a.
  115. Y. Kenzhebayeva, I. Gorbunova, A. Dolgopolov, M.V. Dmitriev, T.S. Atabaev, E.A. Stepanidenko, A.S. Efimova, A.S. Novikov, S. Shipilovskikh, V.A. Milichko, Self-Assembly of Hydrogen-Bonded Organic Crystals on Arbitrary Surfaces for Efficient Amplified Spontaneous Emission, Adv. Photonics Res. (2023) In press.; DOI: 10.1002/adpr.202300173.
  116. V.G. Popova, L.V. Kulik, R.I. Samoilova, D.V. Stass, V.V. Kokovkin, E.M. Glebov, A.S. Berezin, A.S. Novikov, A. Garcia, H.T. Tuan, R.D. Rodriguez, M.N. Sokolov, P.A. Abramov, Noncovalent Dualism in Perylene-Diimide-Based Keggin Anion Complexes: Theoretical and Experimental studies, Inorg. Chem. (2023) In press.; DOI: 10.1021/acs.inorgchem.3c03030.
  117. P. Debnath, C. Majumder, A. Bhattacharya, P. Debnath, S. Roy, A.S. Novikov, M. Roy, T.K. Misra, Crystal Structure of 2-((E)-((Z)-3-(((4-hydroxyphenyl)amino)methylene)-4-oxocyclohexa-1,5-dien-1-yl)diazenyl)benzoic Acid and Synthesis, Spectroscopy, and DFT Study of Its Dibutyltin(IV) Complex, J. Chem. Crystallogr. (2023) In press. DOI: 10.1007/s10870-023-00996-y.
  118. E. I. Chikunova, V. Yu. Kukushkin, A. Yu. Dubovtsev, Non-Friedländer Route to Diversely 3‑Substituted Quinolines through Au(III)-Catalyzed Annulation Involving Electron-Deficient Alkynes, Org. Lett., 25 (2023); doi: 10.1021/acs.orglett.3c03775.
  119. A. A. Sysoeva, A. S. Novikov, V. V. Suslonov, D. S. Bolotin, M. V. Il'in, 2,1,3-Benzoselenadiazole-containing zinc(II) halide complexes: chalcogen bonding in the solid state and catalytic activity in the Schiff condensation, Inorg. Chim. Acta 561 (2024) 121867. DOI: 10.1016/j.ica.2023.121867.
  120. I. N. Klyukin, A. V. Kolbunova, A. S. Novikov, K. Yu. Zhizhin, N. T. Kuznetsov, Theoretical investigation of CB5H6(Hfac) and CB5H5(H2) carboranes: combined MO and QTAIM analysis, Comput. Theor. Chem. 1231 (2024) 114434 DOI: 10.1016/j.comptc.2023.114434.
  121. A. V. Nelyubin, N. K. Neumolotov, N. A. Selivanov, A. Y. Bykov, I. N. Klyukin, A. S. Novikov, A. S. Kubasov, A. P. Zhdanov, K. Y. Zhizhin, N. T. Kuznetsov, Reduction of triple bond in [B12H11NCR] anions by lithium aluminum hydride: a novel approach to the synthesis of N-monoalkylammonio-substituted closo-dodecaborates, Inorganics 12 (2024) 2. DOI: 10.3390/inorganics12010002.
  122. A. Yu. Samsonova, A. Yu. Mikheleva, K. M. Bulanin, N. I. Selivanov, A. S. Mazur, P. M. Tolstoy, C. C. Stoumpos, Y. V. Kapitonov, Internal Vibrations of Pyridinium Cation in One-Dimensional Halide Perovskites and the Corresponding Halide Salts, Molecules, 29 (2024) 78. DOI: 10.3390/molecules29010078.

See also

  1. A. V. Artem'ev, U. A. Kuzmina, A. Yu. Baranov, A. S. Novikov, I. Yu. Bagryanskaya, Ag(I), Au(I) and Au(I)-Ag(I) clusters based on tris[(6-methylpyridin-2-yl)methyl]phosphine, Inorg. Chem. Commun. 161 (2024) 112131. DOI: 10.1016/j.inoche.2024.112131.
  2. A. W. Temesgen, A. A. Sapronov, A. S. Kubasov, A. S. Novikov, T. A. Le, A. G. Tskhovrebov, Synthesis and crystal structure of the adduct between 2-pyridyl­selenyl chloride and isobutyro­nitrile, Acta Crystallogr. E 80 (2024) E80. DOI: 10.1107/S2056989024000938.
  3. A. V. Artem'ev, E. H. Sadykov, S. S. Shilo, A. Yu. Baranov, M. I. Rakhmanova, A. S. Novikov, D. G. Samsonenko, I. Yu. Bagryanskaya, 1D, 2D and 3D networks based on group 11 metal ions and (pyrazin-2-ylmethyl)phosphines: synthesis, metallophilic interactions and emission properties, Inorg. Chim. Acta (2024) In press. DOI: 10.1016/j.ica.2024.121964.
  4. A. S. Zaguzin, A. V. Zaitsev, N. A. Korobeynikov, A. S. Novikov, A. N. Usoltsev, V. P. Fedin, S. A. Adonin, 4,5-diiodo-1-H-imidazole-derived linker ligand and Cu(I) and Co(II) coordination polymers based thereupon, CrystEngComm (2024) In press. DOI: 10.1039/D4CE00072B.
  5. A. Krinochkin, M. Valieva, E. Starnovskaya, N. Slovesnova, A. Minin, A. Belousova, L. Sadieva, O. Taniya, A. Khasanov, A. Novikov, V. Bruskov, S. Vatolina, D. opchuk, P. Slepukhin, V. Sharutin, G. Zyryanov, New Fluorescent Dye for the Detection of Zn2+ in Living Cells and Fixed Sections of the Rat Pancreas, J. Fluoresc. (2024). DOI: 10.1007/s10895-024-03603-1.
  6. M. V. Il’in, Y. V. Safinskaya, D. A. Polonnikov, A. S. Novikov, D. S. Bolotin, Chalcogen- and Halogen-Bond-Donating Cyanoborohydrides Provide Imine Hydrogenation, J. Org. Chem. (2024) In press. DOI: 10.1021/acs.joc.3c02282.
  7. Y. V. Demyanov, T. S. Sukhikh, I. Yu. Bagryanskaya, A. S. Novikov, M. I. Rakhmanova, A. V. Artem'ev, Homo- and heterometallic complexes designed on group 11 metals and tris(6-methyl-2-pyridyl)phosphine: Synthesis, metallophilic interactions and room-temperature phosphorescence, Polyhedron 252 (2024) 116901. DOI: 10.1016/j.poly.2024.116901.
  8. R. Ninayan, U. Markova, E. Nizov, M. Melesova, A. S. Novikov, A. Shishov, Deep eutectic solvents vs. Aqueous acids in metal extraction from animal tissues, Microchem. J., 200 (2024) 110252. DOI: 10.1016/j.microc.2024.110252.
  9. N. A. Korobeynikov, A. N. Usoltsev, M. N. Sokolov, A. S. Novikov, S. A. Adonin, Polymeric polyiodo-chlorotellurates(iv): new supramolecular hybrids in halometalate chemistry, CrystEngComm (2024) In press. DOI: 10.1039/D4CE00088A.
  10. R. Ninayan, U. Markova, E. Nizov, M. Melesova, A. S. Novikov, A. Shishov, Deep eutectic solvents vs. Aqueous acids in metal extraction from animal tissues, Microchem. J., 200 (2024) 110252. DOI: 10.1016/j.microc.2024.110252.
  11. N. A. Korobeynikov, A. N. Usoltsev, M. N. Sokolov, A. S. Novikov, S. A. Adonin, Polymeric polyiodo-chlorotellurates(iv): new supramolecular hybrids in halometalate chemistry, CrystEngComm (2024) In press. DOI: 10.1039/D4CE00088A.
  12. A.S. Novikov, M.V. Il’in, Computational Study on the Route of Cooperative Organocatalysis Utilizing Thiourea and Halogen Bond Donor Mixture, Russ. J. Gen. Chem. 94 (Suppl 1) (2024) S129. DOI: 10.1134/S1070363224140135.
  13. E.A. Dukhnovsky, A.S. Novikov, A.S. Kubasov, A.V. Borisov, N.D. Sikaona, A.A. Kirichuk, V.N. Khrustalev, A.S. Kritchenkov, A.G. Tskhovrebov, Halogen Bond-Assisted Supramolecular Dimerization of Pyridinium-Fused 1,2,4-Selenadiazoles via Four-Center Se2N2 Chalcogen Bonding, Int. J. Mol. Sci. 25 (2024) 3972. DOI: 10.3390/ijms25073972.
  14. A.E. Kopotilova, M.I. Valieva, E.A. Kudryashova, E.S. Starnovskaya, T.N. Moshkina, E.V. Nosova, O.S. Taniya, A.A. Kalinichev, A.S. Novikov, D.S. Kopchuk, P.A. Slepukhin, V.N. Charushin, Methyl- and Methoxy-substituted 2-(Pyridin-2-yl)-4-(4-aminophenyl)quinazolines: Synthesis and Photophysical Properties, Asian J. Org. Chem. (2024) In press. DOI: 10.1002/ajoc.202400135.

See also

  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-COOR+ (R=H or Na), Materials, 15 (2022) 2004; DOI: 10.3390/ma15062004.
  19. 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.
  20. 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.
  21. 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.
  22. 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.
  23. 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.
  24. 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.
  25. 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.
  26. 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.
  27. 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.
  28. 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.
  29. 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.
  30. 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, JSC, 63 (2022) 510-512; DOI: 10.26902/JSC_id91711.
  31. 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.
  32. 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.
  33. 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.
  34. 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.
  35. 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.
  36. 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.
  37. 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.
  38. 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.
  39. 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.
  40. 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.
  41. 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.
  42. A. S. Novikov, Self-healing polymers, Polymers, 14 (2022) 2261; DOI: 10.3390/polym14112261.
  43. 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.
  44. 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.
  45. 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.
  46. 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.
  47. V.V. Suslonov, N.S. Soldatova, D.M. Ivanov, B. Galmés, A. Frontera, G. Resnati, P.S. Postnikov, V.Y. Kukushkin, N.A. Bokach, Diaryliodonium Tetrachloroplatinates(II): Recognition of a Trifurcated Metal-Involving μ3-I···(Cl,Cl,Pt) Halogen Bond, Crystal Growth and Design, 21 (2021), 5360-5372; DOI: 10.1021/acs.cgd.1c00654.
  48. L.E. Zelenkov, A.A. Eliseeva, S.V. Baykov, V.V. Suslonov, B. Galmés, A. Frontera, V.Y. Kukushkin, D.M. Ivanov, N.A. Bokach, Electron belt-to-s-hole switch of noncovalently bound iodine(i) atoms in dithiocarbamate metal complexes, Inorganic Chemistry Frontiers, 8 (2021), 2505-2517; DOI: 10.1039/d1qi00314c.
  49. 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.
  50. 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.
  51. 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.
  52. 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.
  53. 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.
  54. 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.
  55. 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.
  56. 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.
  57. 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.
  58. 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.
  59. 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.
  60. 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.
  61. 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.
  62. 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.
  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.
  75. I. S. Aliyarova, E. Yu. Tupikina, N. S. Soldatova, D. M. Ivanov, P. S. Postnikov, M. Yusubov, V. Yu. Kukushkin, Halogen bonding involving gold nucleophiles in different oxidation states, Inorg. Chem., 61 (2022); 10.1021/acs.inorgchem.2c01858.
  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.
  79. L. E. Zelenkov, D. M. Ivanov, I. A. Tyumentsev, Yu. A. Izotova, V. Yu. Kukushkin, N. A. Bokach, Structure-directing interplay between tetrel and halogen bonding in co-crystal of lead(II) diethyldithiocarbamate with tetraiodoethylene, Int. J. Mol. Sci., 23 (2022) 11870; doi: 10.3390/ijms231911870.
  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.
  82. 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.
  83. 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.
  84. 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.
  85. 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.
  86. 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.
  87. 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.
  88. 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.
  89. 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.
  90. 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.
  91. 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.
  92. N. S. Soldatova, V. V. Suslonov, D. M. Ivanov, M. S. Yusubov, G. Resnati, P. S. Postnikov, V. Yu. Kukushkin, Controlled halogen bond-involving assembly of double-sigma-hole donating diaryliodonium cations and ditopic arene sulfonates, Crystal Growth & Design, 22 (2022); doi: 10.1021/acs.cgd.2c01090.
  93. 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.
  94. 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.
  95. A. D. Sharapov, R. F. Fatykhov, I. A. Khalymbadzha, M. I. Valieva, I. L. Nikonov, O. S. Taniya, D. S. Kopchuk, G. V. Zyryanov, A. P. Potapova, A. S. Novikov, V. V. Sharutin, O. N. Chupakhin, Fluorescent pyranoindole congeners: synthesis and photophysical properties of pyrano[3,2-f], [2,3-g], [2,3-f], and [2,3-e]Indoles, Molecules 27 (2022) 8867; DOI: 10.3390/molecules27248867.
  96. 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.
  97. 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.
  98. Yu. A. Orekhova, A. S. Mikherdov, V. V. Suslonov, V. P. Boyarskiy. Coupling of thiazole-2-amines with isocyanide ligands in bis-(isocyanide) platinum complex: a new type of reactivity, Inorganics, 10 (2022), 221; DOI: 10.3390/inorganics10120221.
  99. 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.
  100. B. G. Sokolov, V. V. Norin, E. A. Sidel’nikova, A. V. Kameshkov, E. V. Sladkovskaya, V. P. Boyarskiy, Cobalt catalysts for hydroformylation and carboalkoxylation: history and commercial prospects. Russ. J. Appl. Chem., 95 (2022), 631–645; DOI: 10.1134/S1070427222050020.
  101. K. K. Geyl, S. O. Baykova, P. A. Andoskin, V. V. Sharoyko, A. A. Eliseeva, S. V. Baykov, K. N. Semenov, V. P. Boyarskiy, Palladium(II) and platinum(II) deprotonated diaminocarbene complexes based on N-(2-pyridyl)ureas with oxadiazole periphery, Inorganics, 10 (2022), 247; DOI: 10.3390/inorganics10120247.
  102. A. S. Mazur, P. M. Tolstoy, K. Sotiriadis, 29Si NMR investigation of the effect of acetic and oxalic acids on Portland-limestone cement hydration, Mater. Sci. Forum, 1071 (2022) 247–252; DOI: 10.4028/p-73l5m1.
  103. 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.
  104. Karcev, D.D., Efremova, M.M., Molchanov, A.P., ...Bunev, A.S., Khochenkov, D.A. Selective and Reversible 1,3-Dipolar Cycloaddition of 2-(2-Oxoindoline-3-ylidene)acetates with Nitrones in the Synthesis of Functionalized Spiroisoxazolidines. Int. J. Mol. Sci. 2022, 23, 12639. DOI: 10.3390/ijms232012639.

New resource saving processes based on organic reactions catalyzed by transition metal complexes

The objective of this project is the improvement of catalytic methods of organic chemistry for more rational resources using. Precatalysts structures and structure–activity relationships will be studied to achieve this goal, and then the detected patterns will be used to develop new resource saving catalyst systems. Homogeneous catalysis is in line with the so-called "green chemistry". Its purpose is more rational using of resources and reducing the harm caused by chemical processes to the environment. Among the principles of green chemistry one directly calls for chemists to give preference to catalytic processes, and a few (such as the minimization of energy consumption or use of more accessible starting compounds and the reduction of the synthetic steps number) indirectly linked to the development of catalytic techniques in organic synthesis.

The research will be concentrated in a few areas of homogeneous metal complexes catalysis, which are actively developing at the moment, namely:

  1. Synthesis of acyclic diamino carbene complexes of palladium(II) (Pd-ADC) and the study of their catalytic activity in many organic reactions;
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  2. Preparation of cobalt and nickel complexes and nanoparticles (including in situ), can catalyze the reduction and the substitution in the aryl chlorides, as well as studying their catalytic capabilities for utilization of persistent organic pollutants - polychlorinated biphenyls (PCB) - and the preparation on their basis precursors for electro polymers;
    br2
  3. Investigation of copper catalyzed C-C and C-N cross-couplings, including the reactions in an aqueous medium.
    br3