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931.
ZHENG Li-Min FU Yan LIN Jian-Jun XIN Xin-QuanCoordination Chemistry State Key Laboratory Department of Chemistry Nanjing University Nanjing Jiangsu China 《中国化学》1994,12(3):243-247
The solid-solid state reactions of o-aminobenzoic acid with Zn(OAc)2.2H2O, Cu(OAc)2 .H2O, Ni(OAc)2.4H2O and Mn(OAc)2.4H2O result in the formation of corresponding complexes M(OAB)2 (M = Zn(Ⅱ), Cu(Ⅱ), Ni(Ⅱ), Mn(IⅡ)). XRD, IR and elemental analysis methods have been used to characterize the solid products. The activation energies of these reactions, which are calculated from the kinetic data obtained by means of the isothermal electrical conductivity measurement method, have been found to increase in the order: Cu(OAc)2.H2O(37.7 kJ.mol-1)~Mn(OAc)2.4H2O (39.7kJ.mol-1) < Zn(OAc)2.2H2O (56.3 kJ.mol-1) < Ni(OAc)2.4H2O (85.2 kJ.mol-1). The trend is related to their crystal structures. 相似文献
932.
The quantum groupsgl
andA
are constructed. The representation theory of these algebras is developed and the universalR-matrix is presented. 相似文献
933.
Yan H 《Physical review letters》1992,68(20):3048-3051
934.
935.
CF3O2自由基和NO反应机理的理论研究 总被引:1,自引:0,他引:1
用密度泛函理论(DFT)的B3LYP方法, 分别在6-31G、6-311G、6-311+G(d)基组水平上研究了CF3O2自由基和NO反应机理. 研究结果表明, CF3O2自由基和NO反应存在三条可行的反应通道, 优化得到了相应的中间体和过渡态. 从活化能看, 通道CH3O2+NO→IM1→TS1→IM2→TS2→CF3O+ONO的活化能最低, 仅为70.86 kJ•mol-1, 是主要反应通道, 主要产物是CF3O和NO2. 而通道CH3O2+NO→IM1→TS3→CF3ONO2和CH3O2+NO→TS4→IM3→TS5→IM4→TS6→CF3O+NOO的活化能较高, 故该反应难以进行. 相似文献
936.
Yan Ziqian 《数学年刊B辑(英文版)》1982,3(1):67-78
In this paper initial value problems and nonlinear mixed boundary value problems for the quasilinear parabolic systems below
$\[\frac{{\partial {u_k}}}{{\partial t}} - \sum\limits_{i,j = 1}^n {a_{ij}^{(k)}} (x,t)\frac{{{\partial ^2}{u_k}}}{{\partial {x_i}\partial {x_j}}} = {f_k}(x,t,u,{u_x}),k = 1, \cdots ,N\]$
are discussed.The boundary value conditions are
$\[{u_k}{|_{\partial \Omega }} = {g_k}(x,t),k = 1, \cdots ,s,\]$
$\[\sum\limits_{i = 1}^n {b_i^{(k)}} (x,t)\frac{{\partial {u_k}}}{{\partial {x_i}}}{|_{\partial \Omega }} = {h_k}(x,t,u),k = s + 1, \cdots N.\]$
Under some "basically natural" assumptions it is shown by means of the Schauder type estimates of the linear parabolic equations and the embedding inequalities in Nikol'skii spaces,these problems have solutions in the spaces $\[{H^{2 + \alpha ,1 + \frac{\alpha }{2}}}(0 < \alpha < 1)\]$.For the boundary value problem with $\[b_i^{(k)}(x,t) = \sum\limits_{j = 1}^n {a_{ij}^{(k)}} (x,t)\cos (n,{x_j})\]$ uniqueness theorem is proved. 相似文献
937.
DNA tile based self-assembly provides an attractive route to create nanoarchitectures of programmable patterns. It also offers excellent scaffolds for directed self-assembly of nanometer-scale materials, ranging from nanoparticles to proteins, with potential applications in constructing nanoelectronic/nanophotonic devices and protein/ligand nanoarrays. This Review first summarizes the currently available DNA tile toolboxes and further emphasizes recent developments toward self-assembling DNA nanostructures with increasing complexity. Exciting progress using DNA tiles for directed self-assembly of other nanometer scale components is also discussed. 相似文献
938.
SYNTHESIS OF ASILICA-SUPPORTED CARBOXYMETHYL CELLULOSE PLATINUM COMPLEX AND ITS CATALYTIC BEHAVIORS FOR HYDROGENATION OF ETHY... 相似文献
939.
YingXinLIU ZuoJunWEI JiXiangCHEN JiYanZHANG XinXueLI XiongHuiWEI 《中国化学快报》2005,16(4):531-533
A novel lanthana-promoted nickel catalyst supported on silica for the liquid phase hydrogenation of m-dinitrobenzene to m-phenylenediamine was prepared by an incipient wetness sequential impregnation method. It was found that Ni-La/SiO2 catalyst exhibited high activity and stability for m-dinitrobenzene hydrogenation. Over this catalyst, the conversion of m-dinitrobenzene and the yield of m-phenylenediamine were up to 97.1% and 93.5%, respectively,at 373 K and 2.6 MPa hydrogen pressure after reaction for 1 h. 相似文献
940.
Huo SJ Li QX Yan YG Chen Y Cai WB Xu QJ Osawa M 《The journal of physical chemistry. B》2005,109(33):15985-15991
Au colloids were used to fabricate nanoscale-tunable Au nanofilms on silicon for surface-enhanced IR absorption bases in both ambient and electrochemical environments. This wet process incorporates the self-assembly of colloidal Au monolayer using 3-aminopropyl trimethoxysilane as the organic coupler with subsequent chemical plating in an Au(III)/hydroxylamine solution. FTIR spectroscopy in transmission mode of the probe species SCN- was used to evaluate the apparent surface enhancement in IR absorption of 2D Au colloid arrays and chemically plated Au particles. The nanostructure of Au films was examined by atomic force microscopy. The IR and AFM results show that the apparent surface enhancement factor (1-2 orders of magnitude) increases with increasing sizes and/or contact, and the severe aggregation of Au nanoparticles may cause the bipolar band shape. Cyclic voltammetry on the Au nanofilm obtained by the above nucleation and growth strategy exhibits a feasible electrochemical stability and behavior. In situ ATR-FTIR measurement of p-nitrobenzoic acid adsorption demonstrates that the as-grown Au film yields rather promising surface enhancement as well. 相似文献