首页> 外文期刊>International journal of organic chemistry >Synthesis and Photophysical Properties of Fluorene or Carbazole-Based Alternating Copolymers Containing Si and Ethynylene Units in the Main Chain
【24h】

Synthesis and Photophysical Properties of Fluorene or Carbazole-Based Alternating Copolymers Containing Si and Ethynylene Units in the Main Chain

机译:主链上含有Si和亚乙炔基单元的芴或咔唑基交替共聚物的合成及光物理性质

获取原文
       

摘要

Alternating copolymerization of 9,9-dihexyl-2,7-dibromofluorene, N-hexyl-2,7-dibromocarbazole (HCz) with diethynyldimethylsilane, diethynyldiphenylsilane, has been investigated using Sonogashira coupling reaction. Photophysical properties of the resulting copolymers were investigated with UV-Vis absorption and photoluminescence spectroscopy. All the copolymers in chloro-form solution showed absorption peaks at 270 - 280 nm with shoulder peaks at around 380 nm derived from π-π* transition or intra-molecular charge transfer through σ-π moiety, respectively. The chloroform solutions of the copolymers showed broad emission peaks at 415 - 425 nm. The emission wave lengths of the copolymers in the solid state (cast film) detected at 360 - 385 nm were remarkably blue-shifted in comparison with those in the chloroform solutions. Hydrosilylation reaction of the copolymers with 1,4-bis(dimethylsilyl)benzene yielded networked copolymers soluble in chloroform, indicating formation of branching polymers. The chloroform solutions of the HCz-based networked copolymers showed bimodal emission derived from new highly energy states in the σ-π conjugation.
机译:已经使用Sonogashira偶联反应研究了9,9-二己基-2,7-二溴芴,N-己基-2,7-二溴咔唑(HCz)与二乙炔基二甲基硅烷,二乙炔基二苯基硅烷的交替共聚。用UV-Vis吸收和光致发光光谱研究了所得共聚物的光物理性质。氯仿溶液中的所有共聚物分别在270-280 nm处出现吸收峰,并在380 nm处出现肩峰,分别是由π-π*跃迁或分子内电荷通过σ-π部分转移引起的。共聚物的氯仿溶液在415-425 nm处显示出宽的发射峰。与氯仿溶液相比,在360-385 nm处检测到的固态(浇铸膜)共聚物的发射波长发生了明显的蓝移。共聚物与1,4-双(二甲基甲硅烷基)苯的硅氢化反应生成可溶于氯仿的网状共聚物,表明形成支化聚合物。 HCz基网络共聚物的氯仿溶液显示出双峰发射,是由σ-π共轭中的新高能态引起的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号