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1.
A. S. Peregudov L. N. Usatova E. I. Smyslova E. I. Fedin D. N. Kravtsov 《Russian Chemical Bulletin》1995,44(8):1513-1519
It has been shown by the19F NMR method that the relative polarities of nitrogenelement bonds in 2-(4-fluorophenyl)benzimidazole and its PhHg and PPh3Au derivatives increase in the order N-H19F NMR. It has been found that these reactions occur by a bimolecular associative mechanism and that the N-H bond is substantially less reactive than the N-Hg and N-Au bonds, which have identical reactivities within the limits of sensitivity of the method used.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1574–1580, August, 1995.This work was carried out with financial support from the Russian Foundation for Basic Research (Project No. 93-03-5528). 相似文献
2.
D. N. Dybtsev M. P. Yutkin E. V. Peresypkina A. V. Virovets Y. Hasegawa H. Nishihara V. P. Fedin 《Russian Chemical Bulletin》2007,56(9):1782-1786
The reaction of Co(NO3)2·6H2O with 1,3,5-benzenetricarboxylic acid (H3btc, trimesic acid) in DMF at 100 °C afforded the coordination polymer [Co3(dmf)6(btc)(Hbtc)(H2btc)]··9H2O (1) (dmf is N,N′-dimethylformamide, DMF). According to the X-ray diffraction study, the metal-organic coordination polymer is composed of
planar honeycomb (6,3) networks, in which the organic benzenetricarboxylate anions and the inorganic Co2+ cations play a role of three-connected nodes. Disordered water molecules are intercalated between the layers. A study of
the magnetic properties showed the presence of a weak antiferromagnetic coupling between the Co2+ ions (S = 3/2).
Dedicated to Academician G. A. Abakumov on the occasion of his 70th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1719–1723, September, 2007. 相似文献
3.
E. V. Chubarova D. G. Samsonenko H. G. Platas F. M. Dolgushin A. V. Gerasimenko M. N. Sokolov Z. A. Starikova M. Yu. Antipin V. P. Fedin 《Journal of Structural Chemistry》2004,45(6):1004-1013
Compounds of trigonal cluster chloroaqua complexes with cucurbit[8]uril were synthesized by slowly evaporating HCl solutions of chalcogenides heterometallic cubane cluster complexes of molybdenum and tungsten with cucurbit[8]uril in air; the complexes were characterized by X-ray diffraction analysis: (H3O)8[Mo3S4(H2O)2.5Cl6.5]2Cl(PdCl4)·(C48H48N32O16)· 29H2O (a = 13.3183(17) Å, b = 13.7104(18) Å, c = 18.225(3) Å; α = 80.263(3)°, β = 77. 958(3)°, γ = 87.149(4)°, V = 3207.4(7) Å3, space group P
, Z = 1, ρ(calc) = 1.900 g/cm3), (H3O)4 [Mo3S4(H2O)3Cl6]2·(C48H48N32O16)3·68H2O (a = 21.413(6) Å, c = 49.832(10) Å; γ = 120°, V = 19788(8) Å3, space group R
, Z = 3, ρ(calc) = 1.695 g/cm3), (H3O)6 [Mo3S4(H2O)3Cl6]2Cl2·(C48H48N32O16)·12H2O (a = 15.881(2) Å, b = 17.191(2) Å, c = 23.276(4) Å; β = 98.865(15)°, V = 6278.7(15) Å3, space group P21/c, Z = 2, ρ(calc) = 1.638 g/cm3), [W3S4(H2O)5Cl4]2·(C48H48N32O16)3·35H2O (a = 21.038(3) Å; α = 61.20(1)°, V = 6762.0(14) Å3, space group R
, Z = 1, ρ(calc) = 1.582 g/cm3). The [Mo3S4(H2O)3Cl6]2− anion complex was isolated as three geometrical isomers.Original Russian Text Copyright © 2004 by E. V. Chubarova, D. G. Samsonenko, H. G. Platas, F. M. Dolgushin, A. V. Gerasimenko, M. N. Sokolov, Z. A. Starikova, M. Yu. Antipin, and V. P. Fedin__________Translated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 6, pp. 1049–1058, November–December, 2004. 相似文献
4.
Elena V Chubarova Denis G. Samsonenko Maxim N. Sokolov Olga A. Gerasko Vladimir P. Fedin Javier G. Platas 《Journal of inclusion phenomena and macrocyclic chemistry》2004,48(1-2):31-35
A new inclusion compound which is a supramolecular adduct of cucurbit[8]uril with two guest molecules of phenylphosphonic acid, PhP(O)(OH)2, included into the cavity as ``two guests in host'' is reported. The guests match both size and hydrophilicity/hydrophobicity requirements. Two phenyl groups of molecules of PhP(O)(OH)2 are directed toward the center of the large hydrophobic cavity whereas the PO(OH)2 groups are outward-looking and bound with each hydrophilic portal of cucurbit[8]uril by a short hydrogen bond. 相似文献
5.
A. V. Virovets N. V. Podberezskaya M. N. Sokolov I. V. Korobkov V. P. Fedin V. E. Fedorov 《Journal of Structural Chemistry》1993,34(2):292-295
The crystal structure was determined for Nb2S4(S2NCEt2)4 obtained in 48% yield by the reaction of Cs4Nb2S4(NCS)8 with NaS2CNEt2 in water: a=21.181(8), b=6.958(1), c=16.623(6) Å, =133.95(2)o, V = 1764(1) Å3, space group C2/m, Z=2, dcalc=1.708 g/cm3. The measurements were carried out on a Syntex P21 diffractometer with CuK radiation. A total of 2536 reflections were measured, of which 990 were used, Raniso=0.0444. The basic fragment in this molecule is [Nb2(2–S2)2]4+, the Nb–Nb distance in which corresponds to a metal-metal single bond. The molecule is partially disordered over two positions about the twofold axis and mirror plane of the C2/m space group. The dithiocarbamate and disulfide ligands with bidentate coordination form a distorted square antiprism about each of the niobium atoms as in NbS2Cl2. The anomalously large S–S bond length in the S2 ligand [2.282(5) Å] may be attributed to inaccuracy in the determination due to disorder.Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated from Zhurnal Strukturnoi Khimii, Vol. 34, No. 2, pp. 134–138, March–April, 1993. 相似文献
6.
The PMR spectra of piazthiol, which is benzo[1,2-c]-[1,2,5]-thiodiazole, and of its- and-nitro, chloro, methyl and amino derivatives are investigated. The effects of these substituents on the chemical shift is in qualitative agreement with the like effects in the benzene series. The parameters of the corresponding PMR spectra are greatly dependent on the electrophilic action of the heterocyclic ring. It is shown that there is conjugation in the thiadiazole ring, although, however, it is much weakened compared with that existing in the benzene ring.For Part II see [10].The authors thank V. F. Bystrov for discussions, and for making the double resonance measurements with-methylpiazthiol in a JNM-C-60 spectrometer. 相似文献
7.
D. N. Dybtsev I. E. Sokolov E. V. Peresypkina V. P. Fedin 《Russian Chemical Bulletin》2007,56(2):225-230
Two new scaffold-like metal-organic coordination polymers, [Zn2ndc2bpe]·DMF and [Zn2ndc2dedpbp] ·4DMF (ndc is 2,6-naphthalenedicarboxylate, bpe is trans-bis(4-pyridyl)ethylene, and dedpbp is 4,4′-diethynyl-4″,4′″-dipyridylbiphenyl), were synthesized by heating stoichiometric
amounts of zinc(II) nitrate, H2ndc, and bpe or dedpbp in DMF. The structures of the polymers were established by X-ray diffraction. Coordination of linear
dicarboxylate ligands to zinc cations gives rise to planar square-grid networks, and additional coordination of the bifunctional
nitrogen-containing ligands results in the formation of scaffold-like triply interpenetrating structures with a primitive
cubic topology.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 219–223, February, 2007. 相似文献
8.
9.
Synthesis and Crystal Structure of Supramolecular Adducts of Macrocyclic Cavitand Cucurbituril with Chromium(III) and Nickel(II) Aqua Complexes 总被引:1,自引:0,他引:1
Samsonenko D. G. Geras'ko O. A. Mit'kina T. V. Lipkowski J. Virovets A. V. Fenske D. Fedin V. P. 《Russian Journal of Coordination Chemistry》2003,29(3):166-174
Supramolecular compounds {[Cr(H2O)6](C36H36N24O12)}(NO3)3 · 13H2O (I) and {[Ni(H2O)6]2(C36H36N24O12)}(SO4)2 · 16H2O (II) were obtained from aqueous solutions of chromium nitrate or nickel sulfate and the macrocyclic cavitand cucurbituril. According to X-ray diffraction analysis data, the cucurbituril molecule is closed from both sides by metal aqua complexes due to the formation of hydrogen bonding between the cucurbituril CO groups and aqua ligands. Compound I has a chain structure, while the structure of compound II is layered. Modes of cucurbituril coordination, depending on the size and charge of the metal cation, are discussed. 相似文献
10.
S.I. Pombrik D.N. Kravtsov B.A. Kvasov E.I. Fedin 《Journal of organometallic chemistry》1977,136(2):185-200
A 19F NMR study of the transmission of electronic effects has been made for the systems Ar2EC6H4F-4 (E = Sb, Bi, CH, N). The fluorine chemical shifts obtained are correlated with the polar constants (Σσo and Σσ) of the substituents, suggesting that electronic effects are transmitted through the SbCar, BiCar and CCar bonds predominantly by an inductive mechanism, whereas the transmission through the NCar bonds is contributed to significantly by classical resonance effects due to competitive conjugation of the lone pair with the aromatic rings, and the substituents therein. A dual parameter correlation of the fluorine chemical shifts with the inductive (σI) and resonance (σoR and σR) parameters of the substituents in the aromatic rings has led to similar conclusions. The inductive transmission through the bridging Sb and Bi atoms has been assigned to the absence of conjugation of lone pair and vacant d-orbitals of the metals with π-electron systems of the aromatic rings. On the basis of the values of the ? coefficients for the correlation equations obtained it has been established that the transmitting ability of the BiCar bonds is close to that of the CalCar bonds and considerably lower than the transmitting ability of the NCar bonds. 相似文献