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3-烷基-4-氨基-1,2,4-三唑-5-硫酮席夫碱的合成和晶体结构表征
引用本文:曲波,文丽荣,曹玮,赵桂龙. 3-烷基-4-氨基-1,2,4-三唑-5-硫酮席夫碱的合成和晶体结构表征[J]. 青岛科技大学学报(自然科学版), 2005, 26(4): 287-290
作者姓名:曲波  文丽荣  曹玮  赵桂龙
作者单位:青岛科技大学化学与分子工程学院,山东青岛266042
基金项目:山东省自然科学基金项目(No.Y2003B01)
摘    要:在酸性条件下,通过缩合反应制备了一系列3-烷基-4-氨基-1,2,4-三唑-5-硫酮席夫碱,用EAI、R1、H NMR和13C NMR确定了结构。通过对化合物IIa X-ray单晶衍射分析表明:在化合物Ⅱ、Ⅲ中的亚胺(—C N—)构型是E构型(反式),其结构是硫酮式互变而非硫醇式。

关 键 词:1,2,4-三唑  席夫碱  晶体结构  合成
文章编号:1672-6987(2005)04-0287-04
修稿时间:2005-01-20

Synthesis and Crystal Structure of 3-Alkyl-4-amino-1,2,4-triazol-5-thione Schiff Bases
QU Bo,WEN Li-rong,CAO Wei,ZHAO Gui-long. Synthesis and Crystal Structure of 3-Alkyl-4-amino-1,2,4-triazol-5-thione Schiff Bases[J]. Journal of Qingdao University of Science and Technology:Natutral Science Edition, 2005, 26(4): 287-290
Authors:QU Bo  WEN Li-rong  CAO Wei  ZHAO Gui-long
Abstract:A series of new Schiff bases of 3-alkyl-4-amino-1,2,4-triazol-5-thione were prepared by condensation reaction in the presence of concentrated hydrochloric acid. The structures of obtained compounds were characterized by EA, IR, ~(1)H NMR and ~(13)C NMR. The X-ray crystallographic analysis of compound IIa indicated that the configuration of the CN double bond in compounds II and III was E and its structure was thione tautomer rather than thiol tautomer.
Keywords:1  2  4-triazol  Schiff base  crystal structure  synthesis
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