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4-(9-蒽基)-6-辛氧基-1,3,5-三嗪-2-胺的合成及其在酸性介质中的光谱行为研究
引用本文:李春丽,李宗耀,徐莉,韩辉,王华.4-(9-蒽基)-6-辛氧基-1,3,5-三嗪-2-胺的合成及其在酸性介质中的光谱行为研究[J].感光科学与光化学,2011(1).
作者姓名:李春丽  李宗耀  徐莉  韩辉  王华
作者单位:河南大学特种功能材料教育部重点实验室;河南大学化学化工学院;
基金项目:国家自然科学基金资助项目(20972041,20672028); 河南省杰出青年基金(104100510011); 教育部新世纪优秀人才支持计划(NCET-05-0610)
摘    要:以2,4-二氯-6-辛氧基-1,3,5-三嗪为原料,经Kumada偶联及胺化两步反应合成了三嗪胺衍生物:4-(9-蒽基)-6-辛氧基-1,3,5-三嗪-2-胺(AOOTA),总产率为38%.通过紫外-可见吸收光谱及荧光光谱研究了氯仿溶液中AOOTA在乙酸(HOAc)及三氟乙酸(TFA)作用下的光谱行为.研究发现AOOTA与HOAc在基态及激发态下均不能发生双氢键作用,而AOOTA与TFA相互作用基态下形成双氢键复合物,激发态下由于分子中蒽基及辛氧基与三嗪环间的C—C单键以及C—O单键的自由旋转,从而使得AOOTA与TFA分子间不能形成有效的氢键相互作用.

关 键 词:4-(9-蒽基)-6-辛氧基-1  3  5-三嗪-2-胺  合成  乙酸  三氟乙酸  吸收  荧光  

Synthesis of 4-(anthracen-9-yl)-6-(octyloxy)-1,3,5-triazin-2-amine and its Spectroscopic Behavior in Acid Medium
LI Chun-li,LI Zong-yao,XU Li,HAN Hui,WANG Hua.Synthesis of 4-(anthracen-9-yl)-6-(octyloxy)-1,3,5-triazin-2-amine and its Spectroscopic Behavior in Acid Medium[J].Photographic Science and Photochemistry,2011(1).
Authors:LI Chun-li  LI Zong-yao  XU Li  HAN Hui  WANG Hua
Affiliation:LI Chun-li1,LI Zong-yao1,XU Li2,HAN Hui1,WANG Hua1,2(1.Key Lab for Special Functional Materials of Ministry of Education,Henan University,Kaifeng 475004,Henan,P.R.China,2.College of Chemistry and Chemical Engineering,P.R.China)
Abstract:The synthesis of aminotriazine derivative,4-(anthracen-9-yl)-6-(octyloxy)-1,3,5-triazin-2-amine(AOOTA) was reported in this paper.With 2,4-dichloro-6-(octyloxy)-1,3,5-triazine as starting material,AOOTA was obtained through Kumada coupling and amination reaction in total yield of 38%.Spectroscopic behaviors of AOOTA with HOAc and TFA in chloroform were investigated by UV-Vis absorption and fluorescence spectra.It is found that the dual hydrogen-bonded interaction between AOOTA and HOAc can not be observed a...
Keywords:4-(anthracen-9-yl)-6-(octyloxy)-1  3  5-triazin-2-amine  synthesis  acetic acid  trifluoroacetic acid  UV-Vis absorption  fluorescence  
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