云南化工2024,Vol.51Issue(9) :39-41.DOI:10.3969/j.issn.1004-275X.2024.09.08

三溴苯并菲的合成方法研究

The Synthesis of Trisubstituted Triphenylene

何丽敏 周萧茂 刘黔希 曾静 李湘广 杨艳华 雷萍
云南化工2024,Vol.51Issue(9) :39-41.DOI:10.3969/j.issn.1004-275X.2024.09.08

三溴苯并菲的合成方法研究

The Synthesis of Trisubstituted Triphenylene

何丽敏 1周萧茂 1刘黔希 1曾静 1李湘广 1杨艳华 1雷萍2
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作者信息

  • 1. 云南省金属有机分子材料与器件重点实验室,昆明学院 化学化工学院,云南 昆明 650214
  • 2. 云南中烟工业有限责任公司技术中心,云南 昆明 650231
  • 折叠

摘要

苯并菲是多环芳烃家族中的一员,它具有大共轭结构、电子迁移率高等优点,同时,还具有盘状液晶高分子材料的结构稳定、高机械强度及良好的液晶性能等,被广泛应用于有机光电材料、高强度材料等领域.从2,3-二氯硝基苯出发,通过乌尔曼反应、还原反应、重氮化反应合成一种具有多卤素的苯并菲衍生物——1,5,9-三溴苯并菲,该化合物由于卤素原子的存在,具有较多的反应位点,可直接应用于其他苯并菲衍生物和高聚体的合成当中.

Abstract

Triphenylene is a member of the family of polycyclic aromatic hydrocarbons,which has the advantages of large conjugate structure and high electron migration rate,as well as the stable structure of disc-shaped liquid crystal polymer materials,high mechanical strength,good liq-uid crystal performance and so on.Therefore,triphenylene and their derivatives are widely used in organic photoelectric materials,high-strength materials,selective permeable membrances and other different fields.In this paper,an intermediate 1,5,9-triphenylene was synthesized through Ullman reaction,reduction reaction and diazotization from the cheap and easily available raw material 2,3-dichlorotronylbenzene.which can be used by follow-up researchers to synthesize other triphenylene derivatives and their polymers.It has a high number of reactive sites due to the presence of halogen atoms and can be directly applied in the synthesis of other triphenylene derivatives and polymers.

关键词

苯并菲/1,5,9-三溴苯并菲/有机合成

Key words

Triphenylene/1,5,9-tribromide triphenylene/Synthesis

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出版年

2024
云南化工
云南省化工研究院 云天化集团有限责任公司 云南煤化工集团有限公司 云南省化学化工学会

云南化工

影响因子:0.272
ISSN:1004-275X
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