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1.
An x-ray diffraction structural analysis was carried out on 1H+,10H+-1,10-diazonia-18-crown-6 diethyldithiophosphate, which exists in the crystal as isolated ionic hydrogen-bonded complexes [H2DA18C6]2+·2(EtO)2PS2
– with strong inter-ion N-HS hydrogen bonds. The centrosymmetric DA18C6 dication has an unusual two-cornered conformation stabilized by a pair of weak intra-ring furcated OH(N)O hydrogen bonds.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 190–192, January, 1991. 相似文献
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Nail Zabirov Sergej Kashevarov Rafael Cherkasov 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4)
Abstract N-(thio)carbonyl(thio)amidophosphates, their open-chain and crown-containing analogues with a C (X) NHP (Y) fragments are NH acids with pKa 8–11 and the effective complexing agents for “soft” ion metals. 相似文献
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Larisa G. Shaidarova Larisa G. Popesku Nikolay A. Ulakhovich Herman C. Budnikov Nail G. Zabirov 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1)
Abstract Crown-containing N-(thio)phosphoryl(thio)ureas are related to a class of NH-acids due to the presence of two acceptor-groups: (thio)phosphorylic and (thio)acylic. In agreement with structure of lariat ether, it was observed a stage corresponding to the step ejection of two H* ion on the potentiometric titration curve of ligand by alkaline. Calculated step ionization constants demonstrate that these compounds are weak acids with relative values of pK1 and pK2. 相似文献
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Zabirov N. G. Sokolov F. D. Cherkasov R. A. 《Russian Journal of General Chemistry》2003,73(4):638-642
Potassium salts of N-(thio)phosphorylthioamides can substitute one, two, or three halogen atoms in chlorinated 1,3,5-triazine molecules to give the products of imidothiyl structure. At low temperature, products of incomplete substitution of halogen in the starting 1,3,5-triazines can be obtained. 相似文献
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Felix D. Sokolov Damir A. Safin Nail G. Zabirov Alexander Yu. Verat Vasiliy V. Brusko Dmitry B. Krivolapov Ekaterina V. Mironova Igor A. Litvinov 《Polyhedron》2006,25(18):3611-3616
The reaction of bis-thiourea o-C6H4[NHC(S)NHP(S)(Oi-Pr)2]2 (1) with iodine, KOH and ClCH2C(O)OCH3 leads to O,O′-diisopropyl-1,3-dihydro-2H-benzimidazol-2-ylideneamidothiophosphate (2) formation. The complex of the potassium salt of compound 2 with 18-crown-6, having the composition [K(18-crown-6)L], has been synthesized. Bis-thiourea [CH2NHC(S)NHP(S)(Oi-Pr)2]2 (6) forms a stable potassium salt, which oxidation by iodine leads to a product of heterocyclization, O,O′-diisopropyl-(1-{[(diisopropoxyphosphorothio)amino]carbonothioyl}imidazolidine-2-ylidene)amidothiophosphate (8), in which one of the thiourea fragments is kept. 相似文献
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Damir A. Safin Dr. Piotr Mlynarz F. Ekkehardt Hahn Prof. Dr. Maria G. Babashkina Felix D. Sokolov Nail G. Zabirov Joanna Galezowska Henryk Kozlowski 《无机化学与普通化学杂志》2007,633(9):1472-1479
Structure and magnetic properties of N‐diisopropoxyphosphorylthiobenzamide PhC(S)‐N(H)‐P(O)(OiPr)2 ( HLI ) and N‐diisopropoxyphosphoryl‐N′‐phenylthiocarbamide PhN(H)‐C(S)‐N(H)‐P(O)(OiPr)2 ( HLII ) complexes with the CoII cation of formulas [Co{PhC(S)‐N‐P(O)(OiPr)2}2] ( 1 ), [Co{PhN(H)‐C(S)‐N‐P(O)(OiPr)2}2] ( 2 ), [Co{PhC(S)‐N(H)‐P(O)(OiPr)2}2{PhC(S)‐N‐P(O)(OiPr)2}2] ( 1a ) and [Co{PhC(S)‐N‐P(O)(OiPr)2}2}(2,2′‐bipy)] ( 3 ), [Co{PhC(S)‐N‐P(O)(OiPr)2}2(1,10‐phen)] ( 4 ), [Co{PhN(H)‐C(S)‐N‐P(O)(OiPr)2}2(2,2′‐bipy)] ( 5 ), [Co{PhN(H)‐C(S)‐N‐P(O)(OiPr)2}2(1,10‐phen)] ( 6 ) were investigated. Paramagnetic shifts in the 1H NMR spectrum were observed for high‐spin CoII complexes with HLI,II , incorporating the S‐C‐N‐P‐O chelate moiety and two aromatic chelate ligands. Investigation of the thermal dependence of the magnetic susceptibility has shown that the extended materials 1‐2 and 6 show ferromagnetic exchange between distorted tetrahedral ( 1 , 2 ) or octahedral ( 1a , 6 ) metal atoms whereas 3 and 5 show antiferromagnetic properties. Compound 4 behaves as a spin‐canted ferromagnet, an antiferromagnetic ordering taking place below a critical temperature, Tc = 115 K. Complexes 1 and 1a were investigated by single crystal X‐ray diffraction. The cobalt(II) atom in complex 1 resides a distorted tetrahedral O2S2 environment formed by the C=S sulfur atoms and the P=O oxygen atoms of two deprotonated ligands. Complex 1a has a tetragonal‐bipyramidal structure, Co(Oax)2(Oeq)2(Seq)2, and two neutral ligand molecules are coordinated in the axial positions through the oxygen atoms of the P=O groups. The base of the bipyramid is formed by two anionic ligands in the typical 1,5‐O,S coordination mode. The ligands are in a trans configuration. 相似文献
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Institute of Physiologically Active Substances, Russian Academy of Sciences, Chernogolovka. Translated from Zhurnal Strukturnoi Khimii, Vol. 33, No. 5, pp. 163–166, September–October, 1992. 相似文献