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911.
Jun WANG Kai Ying LIU Li WANG Ji Ling BAI 《中国化学快报》2006,17(1):49-52
The techniques of combinatorial chemistry have recently been applied to the discovery of new asymmetric catalyst for a variety of organic transformations1-3. Using combina- torial methods, it is straightforward to generate thousands of potential asymmetri… 相似文献
912.
Gu HE Li GUO Li Fang MA 《中国化学快报》2006,17(3):289-292
Dendrimers are known for their well-defined, regular, highly branched architectures with a large number of functional groups1. Recently, dendrimers have been widely researched in different fields, such as molecular light havesting, catalysts, liquid cryst… 相似文献
913.
Jingye Li Fumihiro Muto Akihiro Oshima Masakazu Washio Shigetoshi Ikeda Yoneho Tabata Chihiro Matsuura 《European Polymer Journal》2006,42(6):1222-1228
New proton exchange membranes (PEMs) were prepared by pre-irradiation induced grafting of α-methylstyrene (AMS)/styrene (STY)/divinylbenzene (DVB) into the crosslinked polytetrafluoroethylene (RX-PTFE) films and successively sulfonated. The new PEMs showed the improved glass transition temperature and chemical stability as compared with the PEMs prepared by pre-irradiation induced grafting of STY/DVB. The balance of the cost, grafting kinetic, thermal properties and the properties of the resulted proton exchange membrane is the key point of this work. 相似文献
914.
A multireference configurational interaction method based on the separated electron pair (SEP) wave functions, SEP‐CI approach, has been developed as an approximation to the traditional CASSCF method. It differs from the CASSCF method in that active orbitals are obtained from the SEP wave function without further optimization in the subsequent CI calculations, and the active space is automatically constructed according to the occupation coefficients of SEP natural orbitals. These features make the present SEP‐CI method computationally much less demanding than the CASSCF method. The applicability of the SEP‐CI method is illustrated with sample calculations on the insertion reaction of BeH2 and dissociation energies of LiH, BH, FH, H2O, and N2. © 2005 Wiley Periodicals, Inc. J Comput Chem 27: 39–47, 2006 相似文献
915.
Chun‐Xiang Wang Chen‐Xia Du Zhi‐Feng Li 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(10):m488-m490
In the title compound, [Zn(C17H10N5O)2(H2O)2]·4H2O, cyclic water hexamers forming one‐dimensional metal–water chains are observed. The water clusters are trapped by the co‐operative association of coordination interactions and hydrogen bonds. The ZnII ion resides on a centre of symmetry and is in an octahedral coordination environment comprising two O atoms and two N atoms from two 2′‐(4,5‐diazafluoren‐9‐ylidene)picolinohydrazidate ligands and two water molecules. 相似文献
916.
A large specific surface area perovskite-type mixed oxide PbTiO3 supported cupric oxide was synthesized as a catalyst for NO decomposition and characterized by techniques such as XPS, XRD, H2-TPR before and after NO decomposition reactions. The catalytic properties were tested with a fix-bed micro-reactor. The results showed that the PbTiO3 was inactive for the reactions, but 1wt % Cu/PbTiO3 catalyst gave fairly good activities for NO decomposition at temperature as low as 473 K. Copper species were found well-dispersed but weakly interacted with the support before NO decomposition, and the NO decomposition caused significant change in the environment of the copper species, which became Cu(Ⅰ) and most probably incorporated into surface crystal lattice of the nano-sized PbTiO3. In NO reaction, a large amount of oxygen atoms from the decomposition of NO penetrated into the nano-sized PbTiO3 support and caused small expansion of crystal lattice. The transport of oxygen between the copper species and the catalyst support may be helpful to speed up the kinetic regeneration of active metal sites from oxygen occupancy and resulted in good catalytic performance. 相似文献
917.
A new method for the determination of trace cadmium in water samples by flame atomic absorption spectrometry (FAAS) after
cloud point extraction (CPE) is proposed. The method is based on the complexation of Cd with 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone
(PMBP) in the presence of non-ionic micelles of Triton X-100. The effect of experimental conditions such as pH, concentration
of chelating agent and surfactant, equilibration temperature and time on cloud point extraction was studied. Under the optimum
conditions, the detection limits are 0.64 ng mL±1 with relative standard deviations (RSDs) of 2.1% (n = 10). The proposed method was applied to the determination of trace
cadmium in water samples with satisfactory results. 相似文献
918.
Complete 1H and 13C NMR assignments of four new steroidal glycosides from a gorgonian coral Junceella juncea 总被引:2,自引:0,他引:2
Four new cholest-type steroidal glycosides, junceellosides A-D, isolated from the EtOH/CH(2)Cl(2) extracts of the South China Sea gorgonian coral Junceella juncea, were identified. Complete assignments of the (1)H and (13)C NMR chemical shifts for these compounds were achieved by means of one- and two-dimensional NMR techniques, including (1)H-(1)H COSY, HSQC, HMBC and NOESY spectra. 相似文献
919.
Barium sulfate nanotubes perform excellently in supporting sulfates (Pt(SO4)2, HgSO4, Ce(SO4)2 and Pb(SO4)2) for low temperature catalytic conversion of methane to methanol under strongly acidic conditions in a conventional gas-phase reactor. 相似文献
920.
The aggregation interaction between reduced-denatured egg white lysozymes during refolding procedure in urea solution was studied by means of reducing and non-reducing protein electrophoreses. Results of non-reducing sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) of the supernatant and aggregate precipitate formed in refolding process show that except being refolded to native egg white lysozymes, the reduced-denatured lysozymes can also form the aggregates with molecular weights (MW) being separately about 30.0 and 35.0 kD, while the reducing SDS-PAGE and the refolding results in the presence of sodium dodecyl sulphate show that these aggregates are formed chiefly through the misconnection of disulfide bonds between the reduced-denatured lysozymes, and the aggregate precipitates are formed through the non-covalent interactions between the aggregates with molecular weight being about 30.0 kD. From the results of electrophoresis and size-exclusion chromatographic analyses, it can be inferred that the aggregates with molecular weights being about 30.0 and 35.0 kD are bi-molecular and tri-molecular egg white lysozyme aggregates, respectively. And finally, a suggested refolding mechanism of reduced-denatured egg white lysozymes in urea solution was presented. 相似文献