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941.
ThecombinationofstrippingvoltammetrywithUPDcanleadtotheimprovementofsensitivity ,selectivi tyandreversibilityforelectroanalyticalpurposeandavoidtheuseoftoxicmercuryastheworkelectrode1andthenanalyticalapplicationshavebeendescribed .2 4 Inthiswork ,wedevelo… 相似文献
942.
943.
AIBN/SmCl3/乳酸体系催化甲基丙烯酸甲酯的反向原子转移自由基聚合 总被引:5,自引:0,他引:5
利用稀土金属化合物三氯化钐(SmCl3)和二氯化钐(SmCl2)之间的单电子转移反应,以AIBN/SmCl3/乳酸作为反向原子转移自由基聚合(ReverseATRP)的催化体系,成功地实现了甲基丙烯酸甲酯(MMA)的反向ATRP,并考察了温度、溶剂和组分比对聚合反应的影响.MMA在该体系中的聚合反应是一级反应,所得PMMA的分子量与单体转化率成正比,聚合物的分子量分布较窄(Mw/Mn<1.5),具有活性聚合的特征. 相似文献
944.
基于卟啉对癌细胞的特殊亲和作用和哌嗪化合物的抗肿瘤、抗病毒作用,设计并合成了具有哌嗪结构的新型卟啉化合物5,10,15,20-四[4-(4'-乙基哌嗪基)苯基]卟啉(TEPPPH2),其结构经UV-Vis, 元素分析,1H NMR等手段证明。采用UV-Vis光谱和荧光光谱研究了TEPPPH2和小牛胸腺DNA 的相互作用模式和结合机理。实验发现,TEPPPH2能嵌入到DNA的碱基对中,1个小牛胸腺DNA分子对TEPPPH2分子的最大结合数n约为88,结合常数为8.4×106mol•L-1 。TEPPPH2与DNA的结合数和结合常数大于已知的四(4-N-甲基吡啶基)卟啉和Ca/sal-his、Ni/sal–aln型席夫碱抗癌药物。 相似文献
945.
At different temperatures, the interactions between imidacloprid (IMI) and bovine serum albumin (BSA) were investigated with a fluorescence quenching spectrum, a synchronous fluorescence spectrum, a three-dimensional fluorescence spectrum and an ultraviolet-visible spectrum. The average values of bonding constants (KLB: 3.424 × 10^4 L,mol^-1), thermodynamic parameters (△H: 5.188 kJ,mol^-1, △G^(○—):-26.36 kJ,mol^-1, △S: 103.9 J,K^-1,mol^-1) and the numbers of bonding sites (n: 1.156) could be obtained through Stern-Volmer, Lineweaver-Burk and ther- modynamic equations. It was shown that the fluorescence of BSA could be quenched for its reactions with IMI to form a certain kind of new compound. The quenching belonged to a static fluorescence quenching, with a non-radiation energy transfer happening within a single molecule. The thermodynamic parameters agree with △H〉 0, △S〉0 and△G^(○-)〈0, suggesting that the binding power between IMI and BSA should be mainly a hydrophobic interaction. 相似文献
946.
Xiao‐Ping Chen Anne Buyle Padias H. K. Hall 《Journal of polymer science. Part A, Polymer chemistry》2002,40(12):1929-1936
A non‐olefinic monomer, methyl 1‐bicyclobutanecarboxylate (MBC), was successfully polymerized by the controlled/“living” atom transfer radical polymerization (ATRP) technique, resulting in a well‐defined homopolymer, PMBC, with only cyclobutane ring units in the polymer chain. An AB block copolymer poly(methyl 1‐bicyclobutanecarboxylate)‐b‐polystyrene (PMBC‐b‐PS), having an all‐ring unit segment, was also synthesized with narrow polydispersity and designed number‐average molecular weight in addition to precise end groups. The 1H NMR spectra, glass‐transition temperature, and thermal stability of PMBC, PMBC‐b‐PS, and PS‐b‐PMBC were investigated. The experimental results showed that the cyclobutane rings in the two block polymers improved their thermal stability. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 1929–1936, 2002 相似文献
947.
Two copper complexes [Cu(TTA)2(4,4′‐azpy)] (1) and [Cu‐(TTA)2(3,3′‐azpy)] (2) (HTTA = 1,1,1‐trifluoro‐3‐(2‐thenoyl)‐acetone, 4,4′‐azpy = 4,4′‐azobispyridine, 3,3′‐azpy = 3,3′‐azobispyridine) were synthesized and characterized. The crystal structures were determined by X‐ray diffraction analysis. The crystal 1 belongs to triclinic with space group P1 , a = 0.8515(2) nm, b = 0.9259(2) nm, c = 0.9468(2) nm, a = 66.126(9)°, β = 79.667(9)°, γ = 90.13(1)°, Z = 1, V = 0.6692(2) nm3, Dc = 3.425 g/cm3, γ = 2.113 mm?1, F(000) = 694, R1 = 0.0594, wR2 = 0.1499. The crystal 2 belongs to monoclinic with space group P21/c, a = 1.0661(2) nm, b = 1.4296(3) ran, c = 1.0041(3) nm, β = 114.50(3)°, V = 1.3926(5) nm3, Z = 2, Dc = 1.646 g/ cm3, μ = 1.015 mm?1, F(000) = 694, R1, = 0.0535, wR2 = 0.1113. In the crystals of complexes 1 and 2, the copper atoms have distorted octahedral symmetry. The two compounds possess very similar one‐dimensional linear chains linked through the rodlike 4,4′‐azpy ligands or 3,3′‐azpy ligands. 相似文献
948.
Summary A new stationary phase [bikis(2,6-di-O-pentyl-3-O-hex-6-enyl)-pentakis(2,6-di-O-pentyl-3-O-methyl)-β-CD-polysiloxane] was
synthesized and successfully applied in GC for the separation of chiral and achiral isomers. It possesses high column efficiency
and exhibits excellent separation ability for disubstituted benzenes. Some typical enantiomers and optical isomers are well
separated. The separation behavior of this new phase is characterized and discussed. 相似文献
949.
Jian Zhun JIANG Wei Hong LI Wei Jin ZHOU Hong Cheng GAO* Jin Guang WU Guang Xian XU Department of Applied Chemistry College of Chemistry Molecular Engineering Peking University Beijing 《中国化学快报》2003,14(4):397-400
During the past decades, there has been a renewed interest in the application of solvent extraction to the recovery of Au (I) from cyanide solutions1,2. Among those various extractants, the amine extractants with the addition of organic phosphorus oxide as cosolvent have been widely investigated3,4. Various diluents and modifiers have been selected to optimize the extraction system so as to increase the loading capacity, improve the selectivity and/or reduce emulsification5. Quaternary amm… 相似文献
950.
应用扫描电化学显微镜研究了室温离子液体(Omim·Tf2N)与1,2-二氯乙烷(DCE)混合溶液/水界面上的电子转移反应. 在保持共同离子(Tf2N-)的浓度比恒定及异相电子转移反应由界面电势差所决定的条件下, 研究了离子液体和DCE混合溶液中二茂铁(Fc)与水相中亚铁氰化钾[K4Fe(CN)6]之间异相电子转移反应. 探讨了混合溶液中离子液体的体积分数(xRTIL)的变化对混合溶液/水界面上电子转移反应的影响. 结果表明, 随着xRTIL的减小(从1减小到0.1), Fc在混合溶液中的扩散系数单调递增(从2.730×10-7 cm2·s-1增加到9.131×10-6 cm2·s-1); 而异相电子转移反应速率常数(k)则先逐渐减小(从8.0 mol-1·cm·s-1减小到0.32 mol-1·cm·s-1), 之后又略有增大(从0.32 mol-1·cm·s-1增大到0.48 mol-1·cm·s-1). 对这种现象可能的原因进行了较详细探讨. 相似文献