首页 | 本学科首页   官方微博 | 高级检索  
     检索      

缩合腐植酸/钯催化剂对芳基卤与丙烯酸Heck反应的催化性能研究
引用本文:褚意新,徐启杰,左春山,刘大勇,时文中.缩合腐植酸/钯催化剂对芳基卤与丙烯酸Heck反应的催化性能研究[J].江西师范大学学报(自然科学版),2014,0(2):201-205.
作者姓名:褚意新  徐启杰  左春山  刘大勇  时文中
作者单位:河南中医学院药学院,河南郑州,450046;黄淮学院化学化工系,河南驻马店,463000
基金项目:河南省科技发展计划(112300410184;0611020500;092300410121)资助项目
摘    要:利用N,N-二异丙基碳二亚胺(D IC)结构中的氨基与腐植酸结构中的羧基反应,制得腐植酸缩合产物.缩合反应提高了腐植酸的稳定性能,作为催化剂的载体有利于保持催化剂的活性.然后,通过简便的方法制得了缩合腐植酸负载钯催化剂,研究了该催化剂对芳基卤与乙烯基化合物的Heck反应的催化性能.通过对温度、时间、催化剂用量、溶剂等条件对催化剂催化活性影响的研究,找出该催化剂对芳基卤与乙烯基化合物Heck反应的适宜条件,并用于催化不同取代基芳基卤与乙烯基化合物的Heck反应.结果表明:该催化剂在较温和的条件下对Heck反应也有很高的催化活性.

关 键 词:缩合腐植酸  氯化钯  Heck反应

The Studies on Heck Reaction between Aryl Halide and Acrylic Acid Catalyzed by Using As-Condensed Humic Acid/Palladium Catalyst
CHU Yi-xin,XU Qi-jie,ZUO Chun-shan,LIU Da-yong,SHI Wen-zhong.The Studies on Heck Reaction between Aryl Halide and Acrylic Acid Catalyzed by Using As-Condensed Humic Acid/Palladium Catalyst[J].Journal of Jiangxi Normal University (Natural Sciences Edition),2014,0(2):201-205.
Authors:CHU Yi-xin  XU Qi-jie  ZUO Chun-shan  LIU Da-yong  SHI Wen-zhong
Abstract:Modified humic acid was synthesized from the condensing reaction between amino groups of N,N-diisopropylcarbodiimide(DIC)with carboxyl group of humic acid.The condensing reaction can improve the stability of humic acid thereby enhance the catalytic performance of humic acid supporting Pd catalyst,with which the catalyst was prepared readily by humic acid as support and PdCl2 as Pd resource.Moreover,catalytic properties of the catalyst for Heck reaction of aryl halide with vinyl compounds were studied.Additionally,the effects of temperature,time,catalyst dosage and solvent on catalytic reaction of Heck reaction were investigated,and the activity of catalyst with the different substituted aryl halide and acrylic acid in this reaction was also studied.It was showed that the catalyst had higher catalysis activity.
Keywords:modified humic acid  PdCl2  Heck reaction
本文献已被 CNKI 等数据库收录!
点击此处可从《江西师范大学学报(自然科学版)》浏览原始摘要信息
点击此处可从《江西师范大学学报(自然科学版)》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号