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251.
252.
Solution-phase mixture synthesis has efficiency advantages and favorable reaction kinetics. Applications of this technique, however, have been discouraged by the difficulty in obtaining individual, pure final products by using conventional separation and identification processes. Introduced here is a new strategy for mixture synthesis that addresses the separation and identification problems. Members of a series of organic substrates are paired with a series of fluorous tags of different chain lengths. The tagged starting materials are then mixed and taken through a multistep reaction process. Fluorous chromatography is used to demix the tagged product mixtures on the basis of the fluorine content of the tags to provide the individual pure components of the mixture, which are detagged to release the final products. The utility of fluorous mixture synthesis is demonstrated by the preparation of a 560-membered library of analogues of the natural product mappicine. A seven-component mixture is carried through a four-step mixture synthesis (two one-pot and two parallel steps) to incorporate two additional points of diversity onto the tetracyclic core. Methods for analysis and purification of the intermediates are established for the quality control of the mixture synthesis. 相似文献
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254.
Yunjie Luo Yingming Yao Jinglei Chen Yong Zhang 《Journal of organometallic chemistry》2003,679(1):125-129
Reactions of [N(C6H3i-Pr2-2,6)(SiMe3)]2LnCl(THF) (Ln=Nd, Yb) with two equivalents of MeLi in a mixture solution of toluene and Et2O gave [N(C6H3i-Pr2-2,6)(SiMe3)]2LnCH3(μ-CH3)Li(THF)3·PhCH3 (Ln=Nd (1), Yb (2)) in good isolated yields as crystalline solids. The single-crystal structural analysis of 2 revealed that the coordination geometry of ytterbium ion is best described as a distorted pseudo-tetrahedron. Both 1 and 2 are active for the polymerization of methyl methacrylate to give syndiotactic-rich and high molecular weight polymers (Mn>104) with relatively narrow molecular weight distributions (Mw/Mn<2). 相似文献
255.
光声量热法测定辅酶B12的光解量子产率 总被引:1,自引:0,他引:1
时间可分辨的光声最热法(Time-resolvedphotoacousticcalorimetry;简称PAC)是研究脉冲激光诱发的快速光化学和光生物化学反应过程动力学和热力学信息的一种有效方法[1-5]。本文采用压电陶瓷圆管同时作为样品油和换能器组成的PAC探测系统[6],以波长λ=355nm的脉冲激光(脉冲宽度8ns,脉冲重复频率10Hz)为光源激发辅酶B12甲醇溶液;研究其解量子产率,获得了满意的结果.1实验被测溶液注入两端用石英玻璃封口的压电陶瓷圆管内腔,激光束透过石英窗照射溶液(如图]所示)为标定被测样品的非辐射放热量,利用能在极短的时间内(<l… 相似文献
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257.
Determining PPARγ-ligand binding affinity using fluorescent assay with cis-parinaric acid as a probe
Gao Zhenting Luo Haibin Chen Lili Shen Jianhua CHEN Kaixian JIANG Hualiang SHEN Xu 《中国科学B辑(英文版)》2005,48(2)
Upon the study of small-molecules binding to proteins, the traditional methods for calculating dissociation constants (Kd and Ki) have shortcomings in dealing with the single binding site models. In this paper, two equations have been derived to solve this problem. These two equations are independent of the total concentration or initial degree of saturation of receptor and the activity of the competitive molecule. Through nonlinear fitting against these two equations, Kd value of a probe can be obtained by binding assay, and Ki value of a ligand can be obtained by competitive assay. Moreover, only the total concentrations of receptor([R]t), ligand([L]t) and probe([P]t) are required for the data fitting. In this work, Ki values of some typical ligands of PPARγ were successfully determined by use of our equations, among which the Ki value of PPARγ-LY171883 was reported for the first time. 相似文献
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259.
本文提出一个以(10~(△pe)-1)~(-1)对△pe表示的离子选择电极一次加入标准法结果处理数值表。该表简单明了,不含电极斜率因素,适用于具有各种斜率的电极和不同价态离子的测定。 相似文献
260.
本文提出并研究了用辐射交联方法测定难溶高聚物的分子量问题。不同熔融指数FEP共聚物,辐射交联后,其凝胶化剂量随熔融指数增大而增高。由高温弹模测得FEP的交联G值为1.2。由交联G值和凝胶化剂量计算得FEP的,它与熔融指数的关系为log∞3.5log(1/Ml)·该结果与一般高聚物的本体粘度与分子量关系相一致。 相似文献