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带内取向柔性多醚链苯炔大环合成
引用本文:李全,郑盈,王力,易守兵,程晓红.带内取向柔性多醚链苯炔大环合成[J].有机化学,2012,32(1):81-87.
作者姓名:李全  郑盈  王力  易守兵  程晓红
作者单位:云南大学化学科学与工程学院 教育部自然资源药物化学重点实验室 昆明650091
摘    要:采用分子间Glaser半环闭环法合成了带内取向柔性多醚链的苯炔大环.用1H NMR,13C NMR,HRMS,UV及PL(photduminescence)确证了目标大环结构,凝胶色谱测定了目标大环纯度.经偏光显微镜(POM)和差热分析仪(DSC)测试表明大环没有呈现预期的液晶性质,可能是由于环内柔性链过于拥挤,不能形成与环平面共面结构,以至于难于进行有序堆积的缘故.

关 键 词:苯炔大环  合成  内取向  多醚链

Synthesis of Shape-Persistent Phenyl Ethynylene Macrocycles with Intrannular Flexible Oligooxylethylene Chains
Li,Quan , Zheng,Ying , Wang,Li , Yi,Shoubing , Cheng,Xiaohong.Synthesis of Shape-Persistent Phenyl Ethynylene Macrocycles with Intrannular Flexible Oligooxylethylene Chains[J].Chinese Journal of Organic Chemistry,2012,32(1):81-87.
Authors:Li  Quan  Zheng  Ying  Wang  Li  Yi  Shoubing  Cheng  Xiaohong
Institution:Li,Quan Zheng,Ying Wang,Li Yi,Shoubing Cheng,Xiaohong(School of Chemistry Science and Engineering,Key Laboratory of Medicinal Chemistry for Natural Resourse of Ministry of Education,Yunnan University,Kunming 650091)
Abstract:hape-persistent phenyl ethynylene macrocycles with intraanular flexible oligooxylethylene chains were synthesized by intramolecular Glaser coupling reaction of half rings.The structures of target phenyl ethynylene macrocycles were identifiedby 1H NMR,13C NMR,HRMS,UV and PL(photduminescence),The purity of the target macrocycles was determined by GPC.All the macrocycles are nomesogens as indicated by polarized optical microscopy(POM) and differential scanning calorimetry(DSC),the reason is analyzed as the streric hindrance of the intrannular flexible chains which led to the anordered aggregation of the macrocycles.
Keywords:phenyl ethynylene macrocycle  synthesis  intrannular  oligooxylethylene chain
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