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论文摘要

咔唑肟酯衍生物的合成和光引发性

Synthesis and photoinitiativity of carbazole oxime ester derivatives

作者:谢川(四川大学化工学院);李万舜(四川大学 化工学院,四川 成都 610065);冯岩(四川大学 化工学院,四川 成都 610065)

Author:Xie Chuan(College of chem.Eng.,Sichuan University);李万舜();冯岩()

收稿日期:2008-07-28          年卷(期)页码:2009,41(4):109-113

期刊名称:工程科学与技术

Journal Name:Advanced Engineering Sciences

关键字:咔唑肟酯 合成 正交实验 光引发性能

Key words:carbazole oxime ester ; synthesis ; orthogonal experiment ; photoinitiativity

基金项目:其它

中文摘要

以N-烃基咔唑为原料,经Friedel-Crafts 酰化、成肟和酯化反应,合成了6种咔唑肟酯衍生物。通过正交设计实验,探讨了产物Ⅰ的Friedel-Crafts 酰化的最佳反应条件:N-乙基咔唑为0.02mol时,反应物苯甲酰氯与N-乙基咔唑摩尔配比为1.2.,催化剂AlCl3与N-乙基咔唑摩尔配比为1.2, 25℃下反应3.5h,产率可达94.6%。利用1H NMR,IR,UV和元素分析对目标产物进行了结构表征。并进行了光引发性能测试。

英文摘要

In this paper six carbazole oxime ester derivatives were synthesized through Friedel-Crafts acylation, oximation and esterification from N-alkyl-carbazole. The optimal operation condition of Friedel-Crafts acylation for product Ⅰ was determined by orthogonal experiment: 0.02mol N-ethyl- carbazol, n Benzoyl chloride/n N-ethyl- carbazol=1.2, n AlCl3/n N-ethyl- carbazol=1.2 , at 25 oC for 3.5h. The yield was 94.6%. The structure of the target compounds was characterized by 1HNMR, IR ,UV and elemental analysis. Photoinitiativity of the products was studied .

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