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侧向氟代四环类液晶单体的合成
引用本文:李娟利,安忠维,杜渭松,李建,郑敏燕.侧向氟代四环类液晶单体的合成[J].化学世界,2009,50(9).
作者姓名:李娟利  安忠维  杜渭松  李建  郑敏燕
作者单位:1. 西安近代化学研究所光电材料中心,陕西,西安,710065
2. 成阳师范学院,陕西,咸阳,712000
摘    要:以4-(反式-4-烷基环己基)-2-氟苯硼酸和卤代苯为起始原料,采用Suzuki偶联反应合成了2个系列15个侧向氟取代双烷基环己基联苯类液晶,采用1H NMR、IR和MS对其结构进行了确证。讨论了不同催化剂、反应底物量以及不同的碱对反应结果的影响,结果表明:在强碱碳酸钾作用下,Pd(PPh3)4作催化剂、4-(反式-4-烷基环己基)-2-氟代苯硼酸∶卤代苯(摩尔比)=1.1∶1时,反应选择性和收率较高,产品收率最高达89%。

关 键 词:Suzuki偶联反应  合成  液晶

Synthesis of Lateral Fluorine Substituted 4, 4'-Bis-(trans-4-n-alkylcyelohexyl) Biphenyl Liquid Crystals
LI Juan-li,AN Zhong-wei,DU Wei-song,LI Jian,ZHENG Min-yan.Synthesis of Lateral Fluorine Substituted 4, 4'-Bis-(trans-4-n-alkylcyelohexyl) Biphenyl Liquid Crystals[J].Chemical World,2009,50(9).
Authors:LI Juan-li  AN Zhong-wei  DU Wei-song  LI Jian  ZHENG Min-yan
Affiliation:1.Optical and Electrical Material Center;Xi'an Modern Chemistry Research Institute;Shaanxi Xi'an 710065;China;2.Department of Chemistry;Xianyang Normal University;Shaanxi Xianyang 712000;China
Abstract:Two series of fifteen lateral fluorine substituted by 4,4′-bis-(trans-4-n-alkylcyclohexyl)biphenyl liquid crystals were synthesized via Suzuki coupling reaction with 2-fluoro-4-(trans-4-alkylcyclohexyl)phenylboronic and halobenzenes as starting materials.Their structures were confirmed using ~1H NMR,IR and MS.The influence of various catalysts,various ratio of reactants and bases on the reaction was studied.The results showed that with Pd(PPh_3)_4 as catalyst,2-fluoro-4-(trans-4-alkylcyclohexyl) phenylboronic: halobenzenes=1.1∶1(mole ratio) and potassium carbonate as base was the best choice,and the best yield was 89%.
Keywords:Suzuki cross-coupling reaction  synthesis  liquid crystals  
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