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1.
Deerenberg S Schrekker HS van Strijdonck GP Kamer PC van Leeuwen PW Fraanje J Goubitz K 《The Journal of organic chemistry》2000,65(16):4810-4817
A series of chiral phosphine-phosphite ligands 1-6 have been synthesized and used in the enantioselective palladium-catalyzed reaction of rac-1,3-diphenyl-2-propenyl acetate with dimethyl malonate as nucleophile. Ligands 1a, 2, 3, 5a, 6a, and 6b have been synthesized starting from racemic tert-butylphenylphosphinoborane. The use of dynamically resolved Li phosphide (-)-sparteine provided the optically pure ligands. Crystals of the allylpalladium (6a) complex were obtained, suitable for X-ray crystal structure determination. The X-ray crystal structure of the allylpalladium (6a) complex revealed a longer palladium-carbon bond distance trans to the phosphine moiety indicating that the attack of the nucleophile takes place at the carbon trans to the phosphine moiety. This was confirmed by the fact that the phosphine moiety did not affect the enantioselectivity directly. Under mild reaction conditions, enantioselectivities up to 83% were obtained (25 degrees C) with ligand 1e. Systematic variation of the ligand bridge and the phosphite moiety showed that the configuration of the product is controlled by the atropisomerism of the biphenyl substituent at the phosphite moiety. The conformation of the biphenyl group, in turn, is controlled by the substituent at the chiral carbon in the bridge. Ligands with large bite angles yielded higher enantioselectivities. 相似文献
2.
Gardolinski JE Ramos LP de Souza GP Wypych F 《Journal of colloid and interface science》2000,221(2):284-290
Well-crystallized kaolinite (K) was initially reacted at 60 degrees C with a water/dimethylsulfoxide (DMSO) mixture and the resulting intercalation derivative (K-DMSO) was characterized by powder X-ray diffractometry (PXRD), thermal analysis (simultaneous TG and DSC), and Fourier-transformed infrared spectroscopy (FTIR). Benzamide crystals were then melted with the K-DMSO derivative at 140 degrees C for 4 days, when a gradual displacement of DMSO by benzamide was observed within the interlayer spacing of the modified kaolinite. The resulting material, after extensive washing with acetone, was characterized and compared to the results obtained previously for the K-DMSO composite. Benzamide intercalation proceeded by gradual displacement of DMSO molecules until completion. The structural stabilization of the K-BZ derivative was explained through the establishment of hydrogen bonds between the carbonyl oxygen atoms of the intercalated benzamide and aluminol groups present at the surface of the kaolinite layer. The interlamellar spacing of K-BZ was shown to be possibly occupied by benzamide molecules that were located at a 68 degrees orientation in relation to the layer surface. Unlike most intercalation molecules such as DMSO, variations in the interplanar spacing of kaolinite were consistent with the nonkeying of any other part of the molecule between the aluminosilicate interlayers. Copyright 2000 Academic Press. 相似文献
3.
V. O. Yablonskii 《Russian Journal of Applied Chemistry》2005,78(8):1294-1300
The model of separation of suspensions with a non-Newtonian dispersion medium in a cylindroconical hydrocyclone, which takes into account the effect of the Coriolis force on solid particles, was constructed and applied to analysis of the rheological properties of the dispersion medium on separation of suspensions in hydrocyclones with various working space configurations. 相似文献
4.
A. V. Myshlyavtsev R. T. Samdanchap G. S. Yablonskii 《Reaction Kinetics and Catalysis Letters》1992,48(1):189-193
The simplest catalytic system with surface phase transitions in CSTR has been studied. It is shown that the possible number of steady states is directly determined by that of phase coexistence regions on the phase diagram of the adsorption layer.
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5.
G. S. Yablonskii M. Z. Lazman V. I. Bykov 《Reaction Kinetics and Catalysis Letters》1982,20(1-2):73-77
On the basis of the polynomial to which the system of pseudo-steady-state equations corresponding to the nonlinear single-route mechanism is reduced (kinetic polynomial), the known concepts of stoichiometric number and molecularity have been studied. A set of the minimal-integer stoichiometric coefficients is shown to correspond to the kinetic characteristics in the neighborhood of equilibrium.
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6.
Ya. Yu. Stepanskii N. P. Evmenenko G. S. Yablonskii V. I. Bykov 《Reaction Kinetics and Catalysis Letters》1980,14(3):335-339
Self-oscillation found experimentally in the cool-flame combustion of a model n-heptane-i-octane mixture has been studied in dependence on the composition of the reaction mixture. Calculations based on the CSTR model are in qualitative agreement with experimental data.
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10.
V. I. Bykov V. I. Elokhin G. S. Yablonskii 《Reaction Kinetics and Catalysis Letters》1976,4(2):191-198
The conditions for the existence of several steady states of the surface have been found for the simplest mechanism without the assumption of autocatalysis and without the effect of the medium on the catalyst. A possibility has been shown for the explanation of the multiplicity of steady states, found experimentally in the kinetic region, in terms of mechanisms including interactions between various intermediates.
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