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1.
E. V. Sennikova A. S. Antsyshkina G. G. Sadikov A. V. Bicherov O. Yu. Korshunov G. S. Borodkin M. S. Korobov V. S. Sergienko N. N. Kharabaev A. D. Garnovskii 《Russian Journal of Coordination Chemistry》2008,34(5):315-321
The chelate and molecular complexes of 2-(2-benzazolyl, perimidyl)-indandiones-1,3 were synthesized for the first time. The structures of the ligands (tautomeric forms) and complex compounds were determined from the X-ray diffraction, 1H, 13C NMR, and IR data and the quantum-chemical calculations (RHF SCF in 6-31 G** basis). 相似文献
2.
Russian Journal of Coordination Chemistry - 相似文献
3.
A. é. Mistryukov I. D. Sadekov V. S. Sergienko G. M. Abakarov M. A. Porai-Koshits A. A. Shneider A. D. Garnovskii 《Chemistry of Heterocyclic Compounds》1989,25(12):1407-1409
The crystal and molecular structure of 2-phenylbenzotellurazole is determined by x-ray methods. The heterocyclic fragment of the molecule is planar. The dihedral angle between planes of the heterocycle and the 2-phenyl substituent is 31.2. Somewhat shortened Te-N intermolecular ocntacts (3.43 å) are seen in the crystal. These do not substantially affect the physical properties of the compound.For Communication 3, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1690–1692, December, 1989. 相似文献
4.
I. S. Vasil’chenko T. E. Shestakova V. N. Ikorskii T. A. Kuz’menko V. G. Vlasenko L. N. Divaeva A. S. Burlov A. I. Uraev I. V. Pirog G. S. Borodkin P. B. Chepurnoi I. G. Borodkina O. A. Beletskii O. A. Karpov I. E. Uflyand A. D. Garnovskii 《Russian Journal of Coordination Chemistry》2007,33(3):176-183
Azomethine derivatives of 1-amino-2-thiobenzimidazole (H2L) were synthesized and studied by IR and 1H NMR spectroscopy. Thiobenzimidazoline tautomeric form of these compounds was found to predominate in a solid state and DMSO solution. Novel mono-and binuclear metal chelates M(HL)2 and M2L2 (M = Ni(II), Cu(II), Co(II), Zn(II), Cd(II)) were synthesized on the basis of H2L derivatives and their composition and structures were established from IR, 1H NMR, EXAFS, and magnetochemical data. The composition of coordination sphere was shown to produce no effect on ferromagnetic exchange in binuclear Cu(II) complexes. 相似文献
5.
Yu. A. Simonov N. V. Gérbéléu P. N. Bourosh V. B. Arion A. D. Garnovskii A. N. Sobolev V. A. Alekseenko 《Journal of Structural Chemistry》1990,31(2):365-369
Institute for Applied Physics, Academy of Sciences of the Moldavian SSR. Institute of Chemistry, Academy of Sciences of the Moldavian SSR. Nat. Research Institute for Physics and Organic Chemistry, Rostov State University. Translated from Zhurnal Strukturnoi Khimii, Vol. 31, No. 2, pp. 199–202, 1990. 相似文献
6.
I. S. Vasil’chenko I. G. Borodkina A. S. Burlov N. V. Karpova G. M. Abakarov K. A. Lyssenko G. S. Borodkin I. E. Uflyand A. D. Garnovskii V. I. Minkin 《Russian Chemical Bulletin》2013,62(8):1809-1814
Bis-imines of 2,2′-diaminodiphenylditelluride and 2-tosylamino (9a) and 2-hydroxybenzaldehyde (9b) were prepared and studied by X-ray diffraction, heteronuclear (1H, 13C, 15N, and 125Te) magnetic resonance, and quantum chemical calculations (Pbe1pbe/DGDZVP). According to the X-ray diffraction data, compound 9b in the crystal phase has nonsymmetrical structure: one of the tellurium atoms forms hypervalent bonding with the adjacent oxygen atom, while the second one is not involved in such interaction. The NMR study showed the symmetric molecular structure of imines 9a,b in DMSO-d6 with the tellurium atoms interacting hypervalently with the C=N nitrogen atoms. 相似文献
7.
8.
V. G. Vlasenko A. I. Uraev Ya. V. Zubavichus A. A. Chernyshov A. D. Garnovskii R. K. Mamin 《Bulletin of the Russian Academy of Sciences: Physics》2008,72(4):468-470
A series of copper metallochelates C22H18CuN4O2 X (X = Se, S, O) as models of active centers of natural metalloproteins have been synthesized on the basis of new azomethine ligand systems. The structure of the complexes has been studied by extended X-ray absorption fine-structure spectroscopy. It is shown that, in the metallochelates with X = Se or S, one azomethine chalcogen-containing ligand undergoes tridentate interaction with copper ions, while the other ligand is an acetate group. As a result, a complex with the N2O2 X environment is formed, where one of the oxygen atoms of the acetate group is at a large distance from the metal ion: R = 2.56–2.68 Å. For the metallochelate with X = O, coordination of the acetate group by a copper ion is found to be absent, and only interaction with azomethine ligands having average Cu-N/O distances R = 1.96–2.04 Å is observed. 相似文献
9.
A. I. Uraev L. D. Popov S. I. Levchenkov I. N. Shcherbakov V. G. Vlasenko K. Yu. Suponitskii S. S. Beloborodov D. A. Garnovskii V. A. Kogan 《Russian Journal of Coordination Chemistry》2014,40(9):599-606
The copper(II) and nickel(II) complexes based on bis(azomethine), which is the condensation product of 1-phenyl-3-methyl-4-formyl-5-mercaptopyrazole with 1,3-diaminopropan-2-ol, are synthesized. Bis-azomethines can form both binuclear and mononuclear complexes in which the hydroxy group is not involved in coordination. The binuclear copper(II) complexes with the acetate and pyrazolate bridges exhibit an antiferromagnetic exchange, which strength is determined by the nature of the bridge (2J = ?154 and ?424 cm?1, respectively). The structure parameters of the coordination spheres of the complexes are determined by X-ray absorption spectroscopy. The structure of the CHCl3 solvate of the binuclear copper(II) complex with the pyrazolate bridge is solved by X-ray diffraction analysis (CIF file CCDC 964655). 相似文献
10.
Makarycheva-Mikhailova AV Kukushkin VY Nazarov AA Garnovskii DA Pombeiro AJ Haukka M Keppler BK Galanski M 《Inorganic chemistry》2003,42(8):2805-2813
The reaction between the platinum(IV) complex trans-[PtCl(4)(EtCN)(2)] and the amino alcohols NH(2)CH(2)CH(2)OH, NH(2)CH(2)CH(Me)OH-(R)-(-), NH(2)CH(Ph)CH(2)OH-(R)-(-), NH(2)CH(Et)CH(2)OH-(R)-(-), NH(2)CH(Et)CH(2)OH-(S)-(+), and NH(2)CH(Pr(n)())CH(2)OH proceeds rapidly at room temperature in CH(2)Cl(2) to furnish the amidine complexes [PtCl(4)(HN=C(Et)NH(arcraise;)OH)(2)] (1-6) in good yield (70-80%). The related reaction between the platinum(II) complex trans-[PtCl(2)(EtCN)(2)] and monoethanolamine in a molar ratio of 1:2 in CH(2)Cl(2) results in the addition of 4 equiv of NH(2)CH(2)CH(2)OH per mole of complex to give [Pt(HN=C(Et)NHCH(2)CH(2)OH)(2)(NH(2)CH(2)CH(2)OH)(2)](2+) (7). Formulation of 1-6 is based upon satisfactory C, H, N elemental analyses, electrospray mass spectrometry, IR spectroscopy, and (1)H, (13)C((1)H), (15)N, and (195)Pt NMR spectroscopies, while the structures of trans-[PtCl(4)((Z)-NH=C(Et)NHCH(2)CH(2)OH)(2)] (1), trans-[PtCl(4)((Z)-NH=C(Et)NHCH(2)CH(Me)OH-(R)-(-))(2)] (2), and trans-[PtCl(4)((Z)-NH=C(Et)NHCH(Et)CH(2)OH-(R)-(-))(2)] (4) were determined by X-ray single-crystal diffraction. The Z-amidine configuration of the ligands is preserved in CDCl(3) solutions as confirmed by gradient-enhanced (15)N,(1)H-HMQC spectroscopy and NOE experiments. The amidines, formed upon Pt(IV)-mediated nitrile-amino alcohol coupling, were liberated from their platinum(IV) complexes 1, 3, and 4 by reaction with Ph(2)PCH(2)CH(2)PPh(2) (dppe) giving free NH=C(Et)NHCHRCH(2)OH (R = H 8, Et 9, Ph 10), with the substituents R of different types, and dppe oxides; the P-containing species were identified by (31)P((1)H) NMR spectroscopy. NOESY spectroscopy indicates that the liberated amidines retained the same configuration relative to the C=N double bond, i.e., syn-(H,Et)-NH=C(Et)NHCHRCH(2)OH. The liberated hydroxo-functionalized amidines 8-10 were converted into oxazolines (11-13) in the presence of a catalytic amount of ZnCl(2). A similar catalytic effect has also been reached using anhydrous MSO(4) (M = Cu, Co, Cd), CdCl(2), and AlCl(3). 相似文献