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971.
利用光谱法和分子对接技术研究了不同pH值对牛血清白蛋白(BSA)与茜素红(ARS)键合作用的影响。pH值为4.0的酸性环境引起BSA天然紧缩构象逐渐发生去折叠,BSA的ⅡA区疏水空腔的展开降低了其与ARS的相互作用,键合常数Kb仅为3.39×104L·mol-1。而pH值大于等电点(pI 4.8)或呈现中性时,两者的键合作用增强,Kb增至3.16×106L·mol-1(pH 7.0)。而且,由于氢键和范德华力的键合作用力较强,BSA和ARS的相互作用受表面电荷影响较小,与理论模拟对接结果相吻合。 相似文献
972.
康经武 《分析测试技术与仪器》2014,(3):125-127
就如何理解和看待新时期分析测试中心的定位和发展,如何解决分析测试中心在结构和管理上存在的固有问题提出了粗略的观点.希望对分析测试中心的发展起到抛砖引玉的作用. 相似文献
973.
Nader Ghaffari Khaligh 《催化学报》2014,35(7):1036-1042
3-Methyl-1-sulfonic acid imidazolium hydrogen sulfate has been used as an efficient, halogen-free,and reusable Brnsted acidic ionic liquid catalyst for the synthesis of ethyl-4-aryl/heteryl- hexahydro-trimehtyl-5-oxoquinoline-3-carboxylates via the one-pot condensation of dimedone with aryl/heteryl aldehydes, ethyl acetoacetate, and ammonium acetate under solvent-free conditions. This method has the advantage of being clean and simple, as well as providing the desired product in high yield over a short reaction time. Furthermore, the catalyst could be recycled and reused four times without any discernible reduction in activity. 相似文献
974.
The Keplerate‐type giant nanoporous isopolyoxomolybdate (NH4)42[MoVI72MoV60O372‐(CH3COO)30(H2O)72], denoted {Mo132}, has been used as a catalyst for the synthesis of1,2,4,5‐tetrasubstituted imidazoles by the one‐pot, four‐component thermal reaction of benzil with aromatic aldehydes, primary amines, and ammonium acetate under solvent‐free conditions. The catalyst was prepared according to a previously published literature procedure using inexpensive and readily available starting materials, and subsequently characterized by FT‐IR, UV and X‐ray diffraction spectroscopy, as well as microanalysis. The results showed that {Mo132} exhibited high catalytic activity towards the synthesis of 1,2,4,5‐tetrasubstituted imidazoles, with the desired products being formed in good to high yields. Furthermore, the catalyst was recyclable and could be reused at least three times without any discernible loss in its catalytic activity. Overall, this new catalytic method for the synthesis of 1,2,4,5‐tetrasubstituted imidazoles provides rapid access to the desired compounds following a simple work‐up procedure, and avoids the use of harmful organic solvents. This method therefore represents a significant improvement over the methods currently available for the synthesis of tetrasubstituted imidazoles. 相似文献
975.
A ZnAl2O4@SiO2 nanocomposite was prepared from metal nitrates and tetraethyl orthosilicate by the sol-gel process, and characterized by X-ray diffraction, Fourier transform infrared, transmission electron microscopy, and N2 adsorption-desorption measurements. The nanocomposite was tested as a heterogeneous catalyst for the acetylation of alcohols, phenols, and amines under solvent-free conditions. Under optimized conditions, efficient acetylation of these substrates with acetic anhydride over the ZnAl2O4@SiO2 nanocomposite was obtained. Acetylation of anilines and primary aliphatic amines proceeded rapidly at room temperature, while the reaction time was longer for the acetylation of alcohols and phenols, showing that an amine NH2 group can be selectively acetylated in the presence of alcoholic or phenolic OH groups. The catalyst can be reused without obvious loss of catalytic activity. The catalytic activity of the ZnAl2O4@SiO2 nanocomposite was higher than that of pure ZnAl2O4. The method gives high yields, and is clean, cost effective, compatible with substrates having other functional groups and it is suitable for practical organic synthesis. 相似文献
976.
A ZnAl2O4@SiO2 nanocomposite was prepared from metal nitrates and tetraethyl orthosilicate by the sol-gel process,and characterized by X-ray diffraction,Fourier transform infrared,transmission electron microscopy,and N2 adsorption-desorption measurements.The nanocomposite was tested as a heterogeneous catalyst for the acetylation of alcohols,phenols,and amines under solvent-free conditions.Under optimized conditions,efficient acetylation of these substrates with acetic anhydride over the ZnAl2O4@SiO2 nanocomposite was obtained.Acetylation of anilines and primary aliphatic amines proceeded rapidly at room temperature,while the reaction time was longer for the acetylation of alcohols and phenols,showing that an amine NH2 group can be selectively acetylated in the presence of alcoholic or phenolic OH groups.The catalyst can be reused without obvious loss of catalytic activity.The catalytic activity of the ZnAl2O4@SiO2 nanocomposite was higher than that of pure ZnAl2O4.The method gives high yields,and is clean,cost effective,compatible with substrates having other functional groups and it is suitable for practical organic synthesis. 相似文献
977.
A new coordination compound with formula [Tb(2-TC)3(DMF)]n (1, 2-TC = 2-thio- phenecarboxylic ligand and DMF = dimethylformamide) was synthesized by solvothermal method. The structure of compound 1 was determined by single-crystal X-ray diffraction analyses, and characterized by elemental analyses, IR and powder X-ray diffraction. Structure analysis reveals compound 1, exhibiting a one-dimensional chain structure, crystallizes in triclinic space group P21/c, with a = 9.2751(19), b = 16.490(3), c = 15.865(5) A, β = 118.98(2)°, V= 2122.7(9)A3, D,. = 1.916 g/cm3, Mr= 612.45 (C18H15NO7S3Tb), F(000) = 1196,μ(MoKa) = 3.67 mm-1, Z = 4, R = 0.0616 and wR = 0.0962 for 3865 observed reflections (I 〉 2o(I)), and R = 0.1092 for all data. Meanwhile, the photoluminescent properties of compound 1 were also investigated in the solid state at room temperature. 相似文献
978.
FarzinMarandi 《结构化学》2014,(8):1184-1190
[Pb(TPT)(μ-I)2PbI2(μ-I)2Pb(TPT)] 1(TPT is the abbreviation of 3,5,6-tris(2-pyridyl)-1,2,4-triazine ligand) has been synthesized and characterized by elemental analysis, IR, 1HNMR spectroscopy and studied by thermal and electrochemical properties as well as X-ray crystallography. The single-crystal X-ray data show two different kinds of Pb2+ ions in 1 with coordination numbers of six, Pb1 = PbI6, and five, Pb2 = PbN3I2, with holodirected and hemidirected coordination spheres, respectively. The supramolecular features in 1 are negotiated through the weak but directional Pb···I, C–H···N and C–H···I interactions and aromatic π-π stacking interactions. 相似文献
979.
A new Cd(II) coordination polymer, namely, [Cd3(1,2,3-BTC)2(L)2]·2.25H2O (1, L = 2-(2-chloro-6-fluorophenyl)-1H-imidazo[4,5-A][1,10]phenanthroline and 1,2,3-BTC = 1,2,3-ben- zenetricarboxylate), has been synthesized under hydrothermal conditions. The compound was characterized by single-crystal X-ray diffraction. It crystallizes in triclinic, space group Pī with α = 11.650(2), b = 12.240(2), c = 19.760(4) A, α = 72.01(3), β = 77.11(3), γ = 83.48(3)°, V = 2609.4(9) A3, Z = 2, C56H31Cd3Cl2F2N8O14.25, Mr = 1489.99, Dc = 1.896 g/cm3, F(000) = 1466, μ(MoKa) = 1.401 mm^-1, R = 0.0401 and wR = 0.1104. Compound 1 shows a 1D chain structure, and the neigh- boring 1D chains of 1 are joined together by π···π interactions to result in a 2D supramolecular layer. In addition, the luminescent property of 1 has been studied in the solid state at room temperature. 相似文献
980.
UV-Vis spectrum and the third-order nonlinear optical properties of the chiral camphor-derived β-diketonate have been studied at the B3LYP/6-31G* level. The results showed that the introduction of electron-drawing group-CF3 and-C3F7 on β-diketonate made the strongest absorption peak red-shift and the lowest energy absorption blue-shied. Introduction of-OC2H5 on the benzene or pyridine ring made the lowest energy absorption blue-shift. When the-C2H3 was introduced on the benzene or pyridine ring, the lowest energy absorption was red-shifted. Introduction of electron-donating group on β-diketonate can enlarge their nonlinear optical properties. On the contrary, the introduction of electron-drawing group dropped it down. 相似文献