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81.
Baolong Li Jiangang Ding Jianping Lang Zheng Xu Jiutong Chen 《Journal of Molecular Structure》2002,616(1-3)
The complex [Ni(tn)2{N(CN)2}]ClO4 (tn=trimethylenediamine) has been synthesized and the structure has been determined. The complex forms a one-dimensional chain structure via the bidentate bridging ligand dicyanamide. A two-dimensional networks is formed via interchain hydrogen bond interactions. 相似文献
82.
83.
Yong Ding Baochun Ma Qiang Gao Guixian Li Liang Yan Jishuan Suo 《Journal of molecular catalysis. A, Chemical》2005,230(1-2):121-128
The epoxidation of cyclopentene with hydrogen peroxide catalyzed by 12-heteropolyacids of molybdenum and tungsten (H3PMo12−nWnO40, n = 1–11), 12-tungstophosphoric acid and 12-molybdophosphoric acid combined with cetylpyridinium bromide as a phase transfer reagent was carried out in acetonitrile. Among 13 heteropolyacids investigated, catalyst of H3PMo6W6O40 showed the highest activity, giving a conversion of 60% and a selectivity of 95% in the epoxidation of cyclopentene. The fresh catalysts and the catalysts under reaction condition were characterized by UV–vis, FT-IR and 31P NMR spectroscopy, which has revealed that all of the molybdotungstophosphoric acids were degraded in the presence of hydrogen peroxide to form a considerable amount of phosphorus-containing species. The active species resulted from H3PMo6W6O40 are new kinds of phosphorus-containing species, which is different from {PO4[WO(O2)2]4}3−. 相似文献
84.
Vertically aligned iron oxide nanobelt and nanowire arrays have been synthesized on a large-area surface by direct thermal oxidation of iron substrates under the flow of O(2). The effects of reactive gas pressure, composition, and temperature have been systematically studied. It was found that nanobelts (width, tens of nanometers; thickness, a few nanometers) are produced in the low-temperature region (approximately 700 degrees C) whereas cylindrical nanowires tens of nanometers thick are formed at relatively higher temperatures (approximately 800 degrees C). Both nanobelts and nanowires are mostly bicrystallites with a length of tens of micrometers which grow uniquely along the [110] direction. The growth habits of the nanobelts and nanowires in the two temperature regions indicate the role of growth rate anisotropy and surface energy in dictating the ultimate nanomorphologies. 相似文献
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88.
Recently the hydrogen-bond activated reactions have attracted much attention.1 Takemoto2 reported a highly enantioselective Michael addition of manolate to nitroolefins catalyzed by a bifunctional organocatalyst with tertiary amine and thiourea moiety. As we known,stereoselective conjugate additions of thiols are interesting due to the standpoint of biological and synthetic importance, however, only very limited good results have been obtained except for the works of Shibasaki3, Kanemasa4 and Deng5 et al.In this letter, we report an efficient catalytic asymmetric Michael reactions of thiols to a,a-unsaturated carbonyl compounds promoted by bifunctional organocatalysts. A series of organocatalysts with chiral amine and thiourea structures were designed and synthesized and have been successfully applied in the conjugated additions of thiols to a,a-unsaturated imides and enones.The reactions got quantitative yields and the ee values were up to 84%. It is noteworthy that the a-asymmetric protonation (up to 43% ee) also could be achieved.The Michael addition between aromatic thiols and a,a-unsaturated carbonyl compounds isdescribed as follows:Works to further increase the enantioselectivity is under investigation in our laboratory. 相似文献
89.
The reduction of C = C double bonds is one of the most fundamental synthetic transformations and plays a key role in the manufacturing of a wide variety of bulk and fine chemicals. Hydrogenation of olefinic substrates can be achieved readily with molecular hydrogen in many cases, but transfer hydrogenation methods using suitable donor molecules such as formic acid or alcohols are receiving increasing attention as possible synthetic alternatives because it requires no special equipment and avoids the handling of potentially hazardous gaseous hydrogen. 相似文献
90.
This paper has extended nonequilibrium Monte Carlo (MC) approach to simulate oscillatory shear flow in a lattice block copolymer system. Phase transition and associated rheological behaviors of multiple self-avoiding chains have been investigated. Stress tensor has been obtained based upon sampled configuration distribution functions. At low temperatures, micellar structures have been observed and the underlying frequency-dependent rheological properties exhibit different initial slopes. The simulation outputs are consistent with the experimental observations in literature. Chain deformation during oscillatory shear flow has also been revealed. Although MC simulation cannot account for hydrodynamic interaction, the highlight of our simulation approach is that it can, at small computing cost, investigate polymer chains simultaneously at different spatial scales, i.e., macroscopic rheological behaviors, mesoscopic self-assembled structures, and microscopic chain configurations. 相似文献