苄基咪唑氯镍酸盐的合成、结构及催化醛醇酯化反应活性研究  

Syntheses and Structures of Tetrachloronickelate Benzylimidazolium Salts and Their Activities as Esterifiction Catalyst

作　　者：董思杰[1] 黄亮亮[1] 左萌萌[1] 周明东[1] 

机构地区：[1]辽宁石油化工大学化学与材料科学学院,抚顺113001

出　　处：《化学通报》2016年第7期645-649,共5页Chemistry

基　　金：国家自然科学基金项目(21201095)资助

摘　　要：合成了三种苄基咪唑氯镍酸盐,通过红外光谱、元素分析、1H NMR以及X-射线单晶衍射对其进行结构表征,并研究了其在醛醇酯化反应中的催化活性。结果表明,在优化条件下,苄基咪唑氯镍酸盐对醛醇酯化反应有着较好的催化活性,以1,3-二(4-甲基苄基)咪唑鎓氯镍酸盐为催化剂,通过一步氧化酯化路线可以有效地催化氧化苯甲醛进行酯化反应,产率为80%。Three tetrachloronickelate benzylimidazolium salts were synthesized and characterized by IR spectroscopy,elemental analysis,nuclear magnetic resonance,and single crystal X-ray diffraction analysis. Further more,the compounds were applied as catalysts for oxidative esterification of aldehydes with alcohol. The experimental results showed that tetrachloronickelate benzylimidazolium salt exhibited high catalytic activity in oxidative esterification reaction. Under the optimal reaction conditions,the 80 % yield of methyl benzoate was obtained by using 4-methylbenzylimidazolium tetrachloronickelate as catalyst.

关 键 词：苄基咪唑氯镍酸盐 结构 催化 醛醇酯化 

分 类 号：O643.36[理学—物理化学]