Facile modifications of a polyimide via chloromethylation. I. Novel synthesis of a new photosensitive polyimide

A soluble aromatic polyimide was chloromethylated via a reaction with chloromethyl methyl ether in the presence of tin(IV) chloride to produce a new starting material for the modification of aromatic polyimides. The chemical structure of the resulting polymer was confirmed by ¹H NMR and Fourier transform infrared spectroscopy. The maximum number of chloromethyl groups per repeat unit was 1.81. The chloromethylated polyimide was stable up to 250 °C and soluble in both chloroform and tetrahydrofuran. So that its utilization for further modification could be demonstrated, cinnamic acid was reacted with the formed polyimide, and it produced a new photosensitive polyimide with a cinnamoyl side chain. The photosensitivity of the resulting polyimide was investigated with ultraviolet spectroscopic methods. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 22–29, 2003     

PPG侧链修饰聚酰亚胺的制备与表征

以可溶性聚酰亚胺为反应底物，经氯甲基化反应制得氯甲基化聚酰亚胺，再以氯甲基为活性反应中心，在聚酰亚胺侧链上接枝聚丙二醇单丁醚（PPG），从而得到PPG侧链修饰聚酰亚胺．所制备的产物结构经红外光谱和核磁共振氢谱得以证实．介电常数及吸附脱附测试结果表明：经过大体积侧链PPG修饰后，聚合物的介电常数明显降低，由3．147降低至2．976；比体积和比表面积增大．同时，所制得的聚合物具有优良的溶解性能，在微电子工业中易于加工应用．     

含氧膦结构的可溶性感光聚酰亚胺合成与表征

聚酰亚胺(PI)是一类综合性能优异的功能性材料,广泛应用于航天、航空及电子工业等领域[1].感光聚酰亚胺可以采用光刻工艺,大大简化了其应用加工程序[2,3],因而备受人们所青睐.含查尔酮结构的聚合物对UV辐射敏感度高和化学稳定性好,最近被广泛的研究和应用[4～7].主链含查尔酮结     

二(2,4,4-三甲基戊基)膦酸-上胺205-正庚烷乳状液膜分离钪(Ⅲ)、铁(Ⅲ)和镥(Ⅲ)

本文研究了二（2，4，4-三甲基戊基）膦酸（Cyanex272）-上胺205-正庚烷乳状液膜分离Sc（Ⅲ）、Fe（Ⅲ）和Lu（Ⅲ）。考察了外相酸度、表面活性剂浓度、流动载体浓度及内相盐酸浓度对Sc（Ⅲ）迁移的影响。并探讨了该液膜体系分离Sc（Ⅲ）、Fe（Ⅲ）和Lu（Ⅲ）的可能性，结果表明，该体系对于稀土矿中Sc（Ⅲ）的分离与分析有良好的应用前景。     

Solvent Effect on the Photocatalytic Activity of g-C3N4/BiOBr and its Effect on Degradation of Acetochlor

Russian Journal of Physical Chemistry A - g-C3N4/BiOBr composites were obtained via solvothermal method. XRD, SEM, FTIR, UV–Vis DRS, BET, and BJH methods were used to characterize the...     

Ni-B非晶态合金催化苯丙酮酸加氢合成苯丙氨酸

通过化学还原法制备了纳米非晶态Ni-B合金催化剂,考察了其对苯丙酮酸胺化加氢合成苯丙氨酸的催化性能.结果表明,相对于传统雷尼镍和漆原镍催化剂,非晶态合金催化剂表现出更为优异的活性和选择性,并且当非晶态Ni-B合金负载在SiO2载体上时,其活性和选择性均得到较大提高(高达97.67%).非晶态合金催化剂对苯丙氨酸合成反应表现出较好活性和选择性的原因主要是硼提供部分电子给镍的效应以及非晶态合金颗粒的纳米尺寸效应.     

Asymmetric Epoxidation of Terminal Olefins with Binaphthyl Strapped Porphyrin Catalysts: (‐( Stacking Interaction and Steric Effects on the Enantioselectivities

将两种具有相似手性联萘空腔的手性卟啉1b和2b作为催化剂,对苯乙烯衍生物及非芳香烯烃底物进行了催化不对称环氧化反应。应用理论计算方法研究了底物同两种催化剂之间的作用机理;应用1H NMR探讨了催化剂的手性空腔结构;结果表明芳香烯烃同催化剂的手性联萘基团之间的p-p相互作用是决定该类催化剂对映选择性的重要因素,同时催化剂手性结构的立体位阻效应使该类催化剂具有良好的ee值。     

A novel synthesis of tolunitriles by selective ammoxidation

A new approach to synthesize tolunitriles is reported. Tolunitriles can be prepared by selective ammoxidation of methylbenzyl chlorides prepared by chloromethylation of toluene. The total yields can reach 83% and the selectivity of tolunitriles is almost 100%. This approach provides a new path for preparing alkylbenzonitriles and other aromatic nitriles.     

Synthesis of water‐soluble monotosylated ethylenediamines and their application in ruthenium and iridium‐catalyzed transfer hydrogenation of aldehydes

Synthesis of novel water‐soluble monotosylated ethylenediamines and their application in ruthenium and iridium‐catalyzed transfer hydrogenation of aldehydes are described. Various aldehydes, including electron‐deficient and electron‐rich variants, were reduced with high conversions and chemoselectivity using sodium formate as a hydrogen source in neat water. Copyright © 2011 John Wiley & Sons, Ltd.     

Synthesis of 1,5-dinitroaryl-1,4-pentadien-3-ones under ultrasound irradiation

1,5-Dinitroaryl-1,4-pentadien-3-ones were synthesized with ultrasound irradiation in the presence of K(2)CO(3) as catalyst. The reaction mechanism and the factors influencing the product were also discussed. The present procedure is more convenient with shorter reaction time and higher yields compared with conventional methods.