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一种循环延长1,3,4-噁二唑-苯链的合成方法
引用本文:魏丽莹,孟国云,杨付锐,唐怀军. 一种循环延长1,3,4-噁二唑-苯链的合成方法[J]. 云南民族大学学报(自然科学版), 2014, 0(6): 411-414
作者姓名:魏丽莹  孟国云  杨付锐  唐怀军
作者单位:云南民族大学民族药资源化学国家民委-教育部重点实验室
基金项目:国家自然科学基金(21262046);云南省教育厅理工重点项目(2011Z003);云南民族大学青年基金(11QN05)
摘    要:
1,3,4-噁二唑类化合物因具有独特的生物活性和光电性能而被广泛研究,在医药、有机电子和发光材料等领域具有广泛的应用价值.引入多个1,3,4-噁二唑结构单元,常常可以进一步提高此类化合物的功效性.通过将苯甲醛类化合物上的醛基转化为氰基后,再转化为四唑基,然后由苯四唑类化合物和对甲酰基苯甲酰氯反应生成1,3,4-噁二唑类化合物,此化合物保留了对甲酰基苯甲酰氯带入的醛基,可以进一步地采用相同方法循环反应下去,从而可以得到含有多个1,3,4-噁二唑-苯结构单元的系列链状化合物.

关 键 词:1,3,4–噁二唑  链状化合物  苯甲腈  苯四唑  对甲酰基苯甲酰氯

A synthetic method for extending the organic chain composed of cyclical 1,3,4-oxadiazole-benzene units
WEI Li-ying;MENG Guo-yun;YANG Fu-rui;TANG Huai-jun. A synthetic method for extending the organic chain composed of cyclical 1,3,4-oxadiazole-benzene units[J]. Journal of Yunnan Nationalities University:Natural Sciences Edition, 2014, 0(6): 411-414
Authors:WEI Li-ying  MENG Guo-yun  YANG Fu-rui  TANG Huai-jun
Affiliation:WEI Li-ying;MENG Guo-yun;YANG Fu-rui;TANG Huai-jun;Key Laboratory of Chemistry in Ethnic Medicinal Resources,State Ethnic Affairs Commission and Ministry of Education,Yunnan Minzu University;
Abstract:
Due to particular bioactivities and photoelectric properties,organic compounds containing 1,3,4-oxadiazole have been widely investigated and applied in many fields,such as pharmaceutics,organic electronics and luminescent materials. The performances of these compounds usually would be improved by introducing multiple 1,3,4-oxadiazole groups. In this paper,a series of chain compounds composed of cyclical 1,3,4-oxadiazole-benzene units were synthesized through the aldehyde group on benzene ring being transformed successively into the cyano and 1H-tetrazole group,and then reacting with 4-formylbenzoyl chloride. Such reactions can be recycled continuously due to a new aldehyde group on benzene ring being introduced in the resultant compounds deriving from 4-formylbenzoyl chloride.
Keywords:1,3,4-oxadiazole  chain compound  benzonitrile  5-phenyl-1H-tetrazole  4-formylbenzoyl chloride
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