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171.
Reaction of Os3(CO)10(NCMe)2 and 1,5-cyclooctadiene (C8H12) affords the diene complex Os3(CO)10(η4-C8H12) (1) with the two alkene moieties coordinated to an equatorial and an axial positions of one osmium atom. Thermolysis of 1 in refluxing n-hexane results in a vinylic C-H bond activation to form (μ-H)Os3(CO)9(μ,η4-C8H11) (2) in good isolated yield. The crystal structures of 1 and 2 have been established by an X-ray diffraction study. 相似文献
172.
Alkyl substituted chromium Fischer carbene complexes react with 1,1-diphenylallene in the presence of rhodium(I) catalysts (10 mol%) to yield highly substituted dienyl indenone derivatives. In this process a catalytic chromium(0)-rhodium(I) exchange occurs, four new C-C bonds are created, and four-components (two allenes, the carbene ligand and one CO ligand) are joined in a chemo- and regioselective manner. 相似文献
173.
Hydrolyses of phosphorus halides, (RO)(2)POX where R = H or Me and X = F or Cl, in the gas phase and in the reaction field have been investigated theoretically with ab initio and the density functional theory (DFT). The free energy of activation in the reaction field was also estimated using the Onsager method with a correction of entropy change and basis set superposition error (BSSE). The reaction of (MeO)(2)POF proceeds through a path with bifunctional catalysis regardless of the medium, but the reaction of (MeO)(2)POCl proceeds through bifunctional and general base catalysis in the gas phase and in water, respectively. The estimated free energy barrier of 23 kcal/mol for the hydrolysis of (MeO)(2)POF is in good agreement with the experimental values of 24 kcal/mol, and relative barrier of 3 kcal/mol to the (MeO)(2)POCl is also in good agreement with the experimental values of 5 kcal/mol of diisopropyl phosphorus halides ((Pr(i)O)(2)POX, X = F and Cl). 相似文献
174.
New phases which arise from partial substitution of Ti4+ by Cr3+ and Li+ of the compound La2/3TiO3 have been obtained, giving rise to the series La1.33LixCrxTi2−xO6 (x=0.66, 0.55 and 0.44). These phases adopt a perovskite-type structure as deduced from their structural characterization. Rietveld's analyses of neutron diffraction data show that it is orthorhombic (S.G. Pbnm) with ordered domains. Conductivity has been examined by complex impedance spectroscopy and it increases with increasing lithium and chromium content. These materials behave as mixed conductors with low activation energies. Magnetic susceptibility variation with temperature shows antiferromagnetic interactions at the lowest temperatures. 相似文献
175.
The carbon-fluorine bond of a trifluoromethyl group attached to a π system can be activated by metallic magnesium in the system TMSCl-THF or DMF providing a variety of difluorinated compounds via a selective CF bond cleavage. Thus, trifluoromethyl ketones, α,β-unsaturated ketones, esters, imines, and aromatics can be transformed into the corresponding difluoroenol silyl ethers, enamines, and difluoro(trimethylsilyl)methyl aromatics in good to excellent yields, respectively. This protocol enabled us to synthesize β,β-difluoroamino acids, difluoroheterocycles, and functionalized difluoroacetates. 相似文献
176.
Sergey?P.?BabailovEmail author Lubov?D.?Nikulina 《Journal of inclusion phenomena and macrocyclic chemistry》2005,51(1-2):103-109
1H and 13C NMR measurements are reported for the CDCl3 and CD2Cl2 solutions of [La(NO3)3(18-crown-6)] (I), [Pr(NO3)3(18-crown-6)] (II) and [Ce(NO3)3(18-crown-6)] (III) complexes. Temperature dependencies of the 1H NMR spectra of II have been analyzed using the dynamic NMR methods for multi-site exchange. Two types of conformational dynamic processes in II were identified (the first one with activation enthalpy ΔH
‡=26 ± 4 kJ/mol is conditioned by interconversion of complex enantiomeric form and pseudorotation of macrocycle molecule upon the C
2 symmetry axis, the second one with ΔH
‡=46 ± 5 kJ/mol is conditioned by macrocycle molecule inversion). Studies of the values of the lanthanide-induced shifts revealed that the structure of complexes in solution is similar to that reported for the complex I in the crystal state.This revised version was published online in July 2005 with a corrected issue number. 相似文献
177.
Background: HTLV I Tax is believed to activate viral gene expression by binding bZIP proteins (such as CRIB) and increasing their affinities for proviral THE target sites. Each 21 by THE target site contains an imperfect copy of the intrinsically bent CRE target site (the TRE core) surrounded by highly conserved flanking sequences. These flanking sequences are essential for maximal increases in DNA affinity and transactivation, but they are not, apparently, contacted by protein. Here we employ non-denaturing gel electrophoresis to evaluate TRE conformation in the presence and absence of bZIP proteins, and to explore the role of DNA conformation in viral transactivation.Results: Our results show that the TRE-1 flanking sequences modulate the structure and modestly increase the affinity of a CREB bZIP peptide for the TRE-1 core recognition sequence. These flanking sequences are also essential for a maximal increase in stability of the CREB-DNA complex in the presence of Tax.Conclusions: The CRE-like TRE core and the TRE flanking sequences are both essential for formation of stable CRIB-TRE-1 and Tax-CREB-TRE-1 complexes. These two DNA segments may have co-evolved into a unique structure capable of recognizing Tax and a bZIP protein. 相似文献
178.
Silvia?Faranda Giorgia?Foca Andrea?Marchetti Lorenzo?TassiEmail author Alessandro?Ulrici Claudia?Zucchi 《Journal of solution chemistry》2004,33(10):1181-1197
Kinematic viscosities were measured for 2-butanone + 2-butanol binary liquid mixtures with a capillary Ubbelohde routine viscometer in the temperature range from 273.15 to 353.15 K at atmospheric pressure, and covering the whole miscibility field (0xi1). Experimental data have been correlated by means of different empirical or semiempirical relationships, such as =(T), =(xi), and =(T, xi). Viscosity deviations, , from ideal behavior are negative at all experimental conditions, confirming that structure breaking effects prevail in the liquids. Furthermore, the thermodynamics of viscous flow and excess Gibbs energy of activation of viscous flow, G*E, have been calculated. As an alternative and complementary approach to such investigations, the fluidity () of this binary system has been analyzed by the modified—Batschinski theory. The results are discussed in terms of the specific molecular interactions between the mixture components. 相似文献
179.
L. M. Pisarenko T. V. Maksimova Z. S. Kartasheva O. T. Kasaikina 《Russian Chemical Bulletin》2003,52(7):1500-1503
The temperature effect on the rate of the decomposition of hydroperoxides and the rate of the formation of free radicals in the oxidation of ethylbenzene with molecular oxygen in the presence of -phenylethyl hydroperoxide—cetyltrimethylammonium bromide (CTAB) as a catalytic system for free radical generation was studied by kinetic methods (from the oxygen consumption and hydroperoxide decomposition rates) and the inhibition method involving different acceptors of free radicals. 相似文献
180.
O. M. Shabanov F. O. Ismailova D. G. Maksumova S. M. Gadzhiev A. O. Magomedova 《Russian Journal of Electrochemistry》2006,42(9):986-989
Effects of high-voltage pulses on electrochemical properties of a molten magnesium electrolyte is studied experimentally. It is established that the electroconductivity of the melt subjected to the pulses and the electrolysis current at a constant voltage increase by up to 25%. The relaxation time of nonequilibrium melt reaches a few tens of minutes and under certain conditions its dynamics is oscillatory. 相似文献