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Представительные публикации кафедры ФОХ 2017–2015

Обновлено

2017

D. S. Bolotin, N. A. Bokach, M. Ya. Demakova, V. Yu. Kukushkin, Metal-involving synthesis and reactions of oximes, Chem. Rev., 117 (2017) 13039–13122; DOI: 10.1021/acs.chemrev.7b00264.

R.M. Islamova, M.V. Dobrynin, A.V. Vlasov, A.A. Eremina, M.A. Kinzhalov, I.E. Kolesnikov, A.A. Zolotarev, E.A. Masloborodova, K.V. Luzyanin,"IridiumIJIII)-catalysed cross-linking of polysiloxanes leading to the thermally resistant luminescent silicone rubbers", Catal. Sci. Technol., 7 (2017) 5843–5846; DOI: 10.1039/c7cy02013a.

Adonin S.A., Gorokh I.D., Novikov A.S., Abramov P.A., Sokolov M.N., Fedin V.P. Halogen contacts-induced unusual coloring in Bi(III) bromide complex: anion-to-cation charge transfer via Br•••Br interactions, Chem. Eur. J., 23 (2017) 15612–15616; DOI: 10.1002/chem.201703747.

Z. M. Bikbaeva, D. M. Ivanov, A. S. Novikov, I. V. Ananyev, N. A. Bokach, V. Yu. Kukushkin, Electrophilic–nucleophilic dualism of nickel(II) toward Ni•••I non-covalent interactions: semicoordination of iodine centers via electron belt and halogen bonding via s-hole, Inorg. Chem., 56 (2017) 13562-13578; DOI: 10.1021/acs.inorgchem.7b02224.

N.G. Voron’ko, S.R. Derkach, M.A. Vovk, P.M. Tolstoy, «Complexation of κ-carrageenan with gelatin in the aqueous phase analyzed by 1H NMR kinetics and relaxation», Carbohydr. Polym. 169 (2017) 117–126; DOI: 10.1016/j.carbpol.2017.04.010.

B. Koeppe, S.A. Pylaeva, C. Allolio, D. Sebastiani, E.T.J. Nibbering, G.S. Denisov, H.-H. Limbach, P.M. Tolstoy. Polar solvent fluctuations drive proton transfer in hydrogen bonded complexes of carboxylic acid with pyridines: NMR, IR and ab initio MD study, Phys. Chem. Chem. Phys., 19 (2017) 1010–1028, DOI: 10.1039/C6CP06677A.

S.A. Pylaeva, H. Elgabarty, D. Sebastiani, P.M. Tolstoy, “Symmetry and dynamics of FHF– anion in vacuum, in CD2Cl2 and in CCl4Ab initio MD study of fluctuating solvent-solute hydrogen and halogen bonds”, Phys. Chem. Chem. Phys. 19 (2017) 26107–26120. DOI: 10.1039/C7CP04493C.

D. M. Ivanov, M. A. Kinzhalov, A. S. Novikov, I. V. Ananyev, A. A. Romanova, V. P. Boyarskiy, M. Haukka, V. Yu. Kukushkin. The H2C(X)–X•••X– (X = Cl, Br) halogen bonding of dihalomethanes, Cryst. Growth Des., 17 (2017) 1353–1362, DOI: 10.1021/acs.cgd.6b01754.

M. L. Kuznetsov, V. Yu. Kukushkin. Diversity of reactivity modes upon interplay between Au(III)-bound isocyanides and cyclic nitrones: a theoretical consideration. Dalton Trans., 46 (2017) 786–802, DOI: 10.1039/C6DT03840A;

Z. M. Bikbaeva, A. S. Novikov, V. V. Suslonov, N. A. Bokach, V. Yu. Kukushkin, Metal-mediated reactions between dialkylcyanamides and acetamidoxime generate unusual (Nitrosoguanidinate)Nickel(II) complexes, Dalton Trans., 46 (2017) 10090–10101; DOI:10.1039/C7DT01960B.

A.V. Artem’ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina, “Facile self-assembly of new luminescent clusters containing a silver-centered tetracapped [Ag@Ag4(µ3-P)4] tetrahedron, inscribed within a N12 icosahedron”, Dalton Trans. 46 (2017) 12425–12429; DOI: 10.1039/C7DT02597a.

M. A. Kinzhalov, A. S. Legkodukh, T. B. Anisimova, A. S. Novikov, V. V. Suslonov, K. V. Luzyanin, V. Yu. Kukushkin, Tetrazol-5-ylidene gold(III) complexes from sequential [2 + 3] cycloaddition of azide to metal-bound isocyanides and N4-alkylation, Organometallics, 36 (2017) 3974–3980; DOI: 10.1021/acs.organomet.7b00591.

S. A. Katkova, M. A. Kinzhalov, P. M. Tolstoy, A. S. Novikov, V. P. Boyarskiy, A. Yu. Ananyan, P. V. Gushchin, M. Haukka, A. A. Zolotarev, A. Yu. Ivanov, S. S. Zlotsky, V. Yu. Kukushkin, Diversity of isomerization patterns and protolytic forms in aminocarbene PdII and PtII complexes formed upon addition of N,N’-diphenylguanidine to metal-activated isocyanides, Organometallics, 36 (2017) 4145–4159; DOI: 10.1021/acs.organomet.7b00569.

A. A. Melekhova, A. S. Smirnov, A. S. Novikov, T. L. Panikorovskiy, N. A. Bokach, V. Yu. Kukushkin, Copper(I)-catalyzed 1,3-dipolar cycloaddition of ketonitrones to dialkylcyanamides. A step toward sustainable generation of 2,3-dihydro-1,2,4-oxadiazoles, ACS Omega, 2 (2017) 1380–1391, DOI10.1021/acsomega.7b00130.

K. V. Luzyanin, A. N. Marianov, P. G. Kislitsyn, V. P. Ananikov. Substrate-selective C–H functionalization for the preparation of organosulfur compounds from crude oil-derived components, ACS Omega, 2 (2017), 1419–142, DOI: 10.1021/acsomega.7b00137.

2016

H.-H. Limbach, G. S. Denisov, I. G. Shenderovich, P. M. Tolstoy. Proton Tautomerism in Systems of Increasing Complexity: Examples from Organic Molecules to Enzymes. Tautomerism: Concepts and Applications in Science and Technology, 2016, Wiley–VCH Verlag GmbH & Co. KGaA; ISBN:978-3-527-33995-2.

V. P. Boyarskiy, D. S. Ryabukhin, N. A. Bokach, A. V. Vasilyev, Alkenylation of arenes and heteroarenes with alkynes, Chem. Rev., 116 (2016) 5894–5986; DOI: 10.1021/acs.chemrev.5b00514.

A. S. Mikherdov, M. A. Kinzhalov, A. S. Novikov, V. P. Boyarskiy, I. A. Boyarskaya, D. V. Dar'in, G. L. Starova, V. Yu. Kukushkin, Difference in energy between two distinct types of chalcogen bonds drives regioisomerization of binuclear (Diaminocarbene)PdII complexes, J. Am. Chem. Soc., 138 (2016) 14129–14137; DOI: 10.1021/jacs.6b09133.

D. S. Bolotin, N. A. Bokach, V. Yu. Kukushkin. Coordination chemistry and metal-involving reactions of amidoximes: relevance to the chemistry of oximes and oxime ligands, Coord. Chem. Rev., 313 (2016), 62–93, DOI: 10.1016/j.ccr.2015.10.005.

V. A. Rassadin, D. P. Zimin, G. Z. Raskil’dina, A. Yu. Ivanov, V. P. Boyarskiy, S. S. Zlotskii, V. Yu. Kukushkin. Solvent- and Halide-free Synthesis of Pyridine-2-yl Substituted Ureas through Facile C–H Functionalization of Pyridine N-oxides, Green Chem., 28 (2016) 6630–6636; DOI: 10.1039/C6GC02556K.

D. M. Ivanov, A. S. Novikov, I. V. Ananyev, Yu. V. Kirina, V. Yu. Kukushkin, Halogen bonding between metal center and halocarbon, Chem. Commun., 52 (2016) 5565–5568; DOI: 10.1039/C6CC01107A.

A. S. Novikov, M. L. Kuznetsov, B. G. M. Rocha, A. J. L. Pombeiro, G. B. Shul’pin. Oxidation of olefins with H2O2 catalysed by salts of Group III metals (Ga, In, Sc, Y and La): epoxidation versus hydroperoxidation, Catal. Sci. Technol., 6 (2016) 1343–1356; DOI: 10.1039/C5CY01367D.

T. V. Serebryanskaya, A. S. Novikov, P. V. Gushchin, M. Haukka, R. E. Asfin, P. M. Tolstoy, V. Yu. Kukushkin, Identification and H(D)-bond energies of C–H(D)···Cl interactions in chloride–haloalkane clusters: combined X-ray crystallographic, spectroscopic, and theoretical study, Phys. Chem. Chem. Phys., 18 (2016) 14104–14112; DOI: 10.1039/C6CP00861E.

E. S. Yandanova, D. M. Ivanov, M. L. Kuznetsov, A. G. Starikov, G. L. Starova, V. Yu. Kukushkin, Recognition of S•••Cl chalcogen bonding in metal-bound alkylthiocyanates, Crystal Growth & Design, 16 (2016) 2979–2987; DOI: 10.1021/acs.cgd.6b00346.

M. A. Kinzhalov, S. A. Timofeeva, K. V. Luzyanin, V. P. Boyarskiy, A. A. Yakimanskiy, M. Haukka, V. Yu. Kukushkin. Palladium(II)-mediated addition of benzenediamines to isocyanides. Generation of three types of diaminocarbene ligands depending on isomeric structure of the nucleophile, Organometallics, 35 (2016) 218–228; DOI: 10.1021/acs.organomet.5b00936

V. N. Mikhaylov, V. N. Sorokoumov, K. A. Korvinson, A. S. Novikov, I. A. Balova, Synthesis and simple immobilization of palladium(II) acyclic diaminocarbene complexes on polystyrene-support as efficient catalysts for Sonogashira and Suzuki–Miyaura cross-coupling, Organometallics, 35 (2016) 1684–1697; DOI: 10.1021/acs.organomet.6b00144.

D. S. Bolotin, V. K. Burianova, A. S. Novikov, M. Ya. Demakova, С. Pretorius, P. P. Mokolokolo, A. Roodt, N. A. Bokach, V. V. Suslonov, A. P. Zhdanov, K. Yu. Zhizhin, N. T. Kuznetsov, V. Yu. Kukushkin, Nucleophilicity of oximes based upon addition to а nitrilium closo-decaborate cluster, Organometallics, 35 (2016) 3612–3623; DOI: 10.1021/acs.organomet.6b00678.

T. B. Anisimova, M. A. Kinzhalov, M. L. Kuznetsov, M. F. C. Guedes da Silva, A. A. Zolotarev, V. Yu. Kukushkin, A. J. L. Pombeiro, K. V. Luzyanin, 1,3-Dipolar cycloaddition of nitrones to gold(III)-bound isocyanides, Organometallics, 35 (2016) 3569–3576; DOI: 10.1021/acs.organomet.6b00635.

2015

V. P. Boyarskiy, N. A. Bokach, K. V. Luzyanin, V. Yu. Kukushkin, Metal-mediated and metal-catalyzed reactions of isocyanides, Chem. Rev., 115 (2015) 2698–2779; DOI: 10.1021/cr500380d.

S. A. Timofeeva, M. A. Kinzhalov, E. A. Valishina, K. V. Luzyanin, V. P. Boyarskiy, T. M. Buslaeva, M. Haukka, V. Yu. Kukushkin. Application of palladium complexes bearing acyclic amino(hydrazido)carbene ligands as catalysts for copper-free Sonogashira cross-coupling, J. Catal., 329 (2015) 449–456; DOI: 10.1016/j.jcat.2015.06.001.

V. A. Rassadin, V. P. Boyarskiy, V. Yu. Kukushkin. Facile gold-catalyzed heterocyclization of terminal alkynes leading to substituted 2-amino-1,3-oxazoles, Org. Lett., 17 (2015) 3502–3505; DOI: 10.1021/acs.orglett.5b01592.

I. G. Shenderovich, S. B. Lesnichin, C. Tu, D. N. Silverman, P. M. Tolstoy, G. S. Denisov, H.-H. Limbach. NMR studies of active site properties of human carbonic anhydrase II using 15N labeled 4-methylimidazole as a local probe and histidine hydrogen bond correlations, Chem. Eur. J., 21 (2015) 2915–2929; DOI: 10.1002/chem.201404083.

D. S. Bolotin, M. Ya. Demakova, A. S. Novikov, M. S. Avdontceva, M. L. Kuznetsov, N. A. Bokach, V. Yu. Kukushkin. Bifunctional reactivity of amidoximes observed upon nucleophilic addition to metal-activated nitriles, Inorg. Chem., 54 (2015) 4039–4046; DOI: 10.1021/acs.inorgchem.5b00253.

A. S. Smirnov, A. S. Kritchenkov, N. A. Bokach, S. I. Selivanov, V. V. Gurzhiy, M. L. Kuznetsov, A. Roodt, V. Yu. Kukushkin. Regio- and stereoselective 1,3-dipolar cycloaddition of cyclic azomethine imines to platinum(IV)-bound nitriles giving Δ2-1,2,4-triazoline species, Inorg. Chem., 54 (2015) 11018–11030; DOI: 10.1021/acs.inorgchem.5b02246.

S. Pylaeva, C. Allolio, B. Koeppe, G.S. Denisov, H.-H. Limbach, D. Sebastiani, P.M. Tolstoy. Proton transfer in short hydrogen bonded complex caused by solvation shell fluctuations: ab initio MD and NMR/UV study of an (OHO)-bonded system, Phys. Chem. Chem. Phys., 17 (2015) 4634–4644; DOI: 10.1039/C4CP04727C.

A. S. Antonov, A. F. Pozharskii, V. A. Ozeranskii, A. Filarowski, K. Yu. Suponitsky, P. M. Tolstoy, M. A. Vovk. Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the proton sponge coin, Dalton Trans., 44 (2015) 17756–17766; DOI: 10.1039/C5DT02482J.

T. V. Serebryanskaya, A. S. Novikov, P. V. Gushchin, A. A. Zolotarev, V. V. Gurzhiy, V. Yu. Kukushkin. Coupling of platinated triguanides with platinum-activated nitriles as a novel strategy for generation of dimetallic systems, Dalton Trans., 44 (2015) 6003–6011; DOI: 10.1039/C4DT03870C.

Т. V. Serebryanskaya, A. S. Lyakhov, L. S. Ivashkevich, J. Schur, C. Frias, A. Prokop, I. Ott, Gold(I) thiotetrazolates as thioredoxin reductase inhibitors and antiproliferative agents, Dalton Trans., 44 (2015) 1161–1169; DOI: 10.1039/c4dt03105a.

A. N. Chernyshev, M. V. Chernysheva, P. Hirva, V. Yu. Kukushkin, M. Haukka. Weak aurophilic interactions in a series of Au(III) double salts, Dalton Trans., 44 (2015) 14523–14531; DOI: 10.1039/c4dt03167a.

Ответственный за содержание сайта Института химии: Роман Зумберов, r.zumberov@spbu.ru