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961.
表面活性剂在非极性溶剂中形成的反胶束在催化反应、光化学、蛋白质苹取分离等方面有着广泛的应用问.这些应用与反胶束的性质有着密切的关系,而增溶水后的反胶束其形状和大小都会发生很大的变化.增溶不同水量的反胶束的微极性、酸碱性、微勤度等已有不少文献报导[2-5].一些不溶于非极性溶剂而溶于水的物质可以溶解在非极性溶剂中的反胶束核心水团中,这个现象被称为二次增溶.其中,电解质的二次增溶对于研究配体转换反应。酶催化反应问及改变反胶束内部的微环境有着十分重要的作用,Aebi和Weibush回首先研究了有水存在时N。CI在A… 相似文献
962.
The hexanuclear tungsten cluster complex [W6(3-Cl)8Cl6]2–,1 was isolated as a salt of the cation (MeO2CCH2)2N(H)CH2CH2N(CH2CO2Me)2+, EDTEH+, by crystallization from methanol solvent of the product obtained from the reaction of (H3O)2[W6(3-Cl)8Cl3] with the disodium salt of ethylenediaminetetraacetic acid. The compound was charcterized by single-crystal X-ray diffraction analysis. The cluster anion contains an octahedral arrangement of six tungsten atoms with chloride ligands bridging the eight triangular faces of the cluster and one chloride ligand terminally coordinated to each of the six tungsten atoms. The cation (EDTEH)+ achieves its positive charge by protonation of one of the nitrogen atoms. Crystal data: space group = P21/a,a=10.689(2) Å,b=22.931(6) Å,c=12.093(3) Å, =98.41(2)°,Z=2, 2476 reflections,R=0.028. 相似文献
963.
Horner-Emmons reaction of phosphonate amides with aldehydes leads to generation of o-substituted aryl-acrylamides. These compounds have been shown to be useful to quickly establish structure-activity relationships (SAR) for soluble guanylyl cyclase (sGC) activator drug discovery. 相似文献
964.
John T. Gupton John E. Gall Steve W. Riesinger Stanton Q. Smith Kathy M. Bevirt James A. Sikorski Maria L. Dahl Zdenek Arnold 《Journal of heterocyclic chemistry》1991,28(5):1281-1285
An alternative preparation of a 2-iminovinamidinium salt from phosphonoacetic acids is described along with its application to the synthesis of 5-formylpyrimidines and masked 4-formylpyrazoles. 相似文献
965.
966.
967.
Chen C Huang D Zhang X Chen F Zhu H Liu Q Zhang C Liao D Li L Sun L 《Inorganic chemistry》2003,42(11):3540-3548
A reaction system consisting of terephthalic acid, NaOH, inorganic Mn(II) or Mn(III) salt, and salicylidene alkylimine resulted in dinuclear manganese complexes (salpn)(2)Mn(2)(mu-phth)(CH(3)OH)(2) (1, salpn = N,N'-1,3-propylene-bis(salicylideneiminato); phth = terephthalate dianion), (salen)(2)Mn(2)(mu-phth)(CH(3)OH)(2) (2, salen = N,N'-ethylene-bis(salicylideneiminato)), (salen)(2)Mn(2)(mu-phth)(CH(3)OH)(H(2)O) (3), and (salen)(2)Mn(2)(mu-phth) (4), while the absence of NaOH in the reaction led to a mononuclear Mn complex (salph)Mn(CH(3)OH)(NO(3)) (5, salph = N,N'-1,2-phenylene-bis(salicylideneiminato)). In addition, a trinuclear mixed metal complex H[Mn(2)Na(salpn)(2)(mu-OAc)(2)(H(2)O)(2)](OAc)(2) (6) was obtained from the reaction system by using maleic acid instead of terephthalic acid. Five-coordinate Mn ions were found in 4 giving rise to an intermolecular interaction and constructing a one-dimensional linear structure. Antiferromagnetic exchange interactions were observed for 1-3, and a total ferromagnetic exchange of 4 was considered to stem from intermolecular magnetic coupling. (1)H NMR signals of phenolate ring and alkylene (or phenylene) backbone of the diamine are similar to those reported in the literature, and the phth protons are at -2.3 to -10.1 ppm. Studies on structure, bond valence sum analysis, and magnetic properties indicate the oxidation states of the Mn ions in 6 to be +3, which are also indicated by ESR spectra in dual mode. Ferromagnetic exchange interaction between the Mn(III) sites was observed with J = 1.74 cm(-1). A quasireversible redox pair at -0.29V/-0.12V has been assigned to the redox of Mn(2)(III)/Mn(III)Mn(II), implying the intactness of the complex backbone in solution. 相似文献
968.
本文介绍了用高效液相色谱法分离测定甜菊糖甙的四种成分,测定了各成分的相对百分含量及甜菊饮料制品中各糖甙成分及糖类的含量,并做了精密度和回收率的验证。该法简便快速,效果良好。色谱条件为:μ-Bondapak NH_2往,柱前加Bondapak AX/Corasil预柱;乙腈:0.02M(NH_4))2 HPO_4水溶液=75:25作流动相,流速为2.0ml·min~(-1);示差折光检测。 相似文献
969.
Ging-Ho Hsiue Wen-Kuei Huang Hsiao-Lung Chu 《Journal of polymer science. Part A, Polymer chemistry》1989,27(13):4397-4402
Differential scanning calorimetry was used to trace the heat of decomposition of the peracid groups (ΔHd) in the oxidized EVA-g-AA resin. From the correlation between ΔHd and the oxidation capacity measured by iodometry, it was found that 35 ± 5 cal of energy evolved per miliequivalent of peracid group decomposed. The ΔHd values are also useful in finding the optimum condition for oxidation of acid groups and can be used to investigate the distribution of active peracid groups across the matrix. The stability and the activation energy of decomposition of grafted type peracid resin were also studied, where the activation energy of decomposition was calculated to be 13.4 kcal/mol. 相似文献
970.
In this study, a series of beadlike and hydrophilic supports containing reactive cyclic carbonate groups for enzyme immobilization
were prepared via reverse-phase suspension copolymerization of the aqueous solutions of vinylene carbonate (VCA), acrylamide
(AA), and N,N′-methylene bisacrylamide in paraffin oil. The supports were used as a matrix for immobilization of trypsin and showed a considerable
capacity to couple with trypsin and reasonable retention of activity for the immobilized trypsin, depending on the immobilization
conditions, such as the content of VCA structural units, reaction time, and pH of the medium. 相似文献