首页> 外文期刊>Dyes and Pigments >Terpyridine-based donor-acceptor metallo-supramolecular polymers with tunable band gaps: Synthesis and characterization
【24h】

Terpyridine-based donor-acceptor metallo-supramolecular polymers with tunable band gaps: Synthesis and characterization

机译:带隙可调的基于吡啶的供体-受体金属超分子聚合物:合成与表征

获取原文
获取原文并翻译 | 示例
           

摘要

Three new building blocks containing the electron-donor fused-ring motifs carbazole, dithienosilole (DTS) and dithienopyrrole (DTP) and the 2,2':6',2 ''-terpyridine electron-acceptor motif were designed and synthesized. Directed by transition metal ions, the self-assembly of the building blocks triggered polymerization to form the corresponding metallo-supramolecular polymers PCzTPY, PSiTPY and PNTPY, respectively. The UV-vis absorption maxima of the building blocks occur at long wavelengths (351, 368 and 430 nm for CzTPY, SiTPY and NTPY, respectively), which arises from intramolecular charge transfer (ICT) transitions. However, the absorption maxima of their corresponding metallosupramolecular polymers are clearly red-shifted (to 394, 431 and 509 nm for PCzTPY, PSiTPY and PNTPY, respectively), which is caused by the incorporation of the transition metal ion into the backbones of the target polymers. Based on the above strategies, the resulting metallo-polymers exhibit reduced energy gaps, which are 2.07,1.97 and 1.56 eV for the PCzTPY, PSiTPY and PNTPY metallo-supramolecular polymers, respectively. (C) 2016 Elsevier Ltd. All rights reserved.
机译:设计并合成了三个新的构建基块,它们分别包含咔唑,二噻吩甲硅醇(DTS)和二噻吩并吡咯(DTP)和2,2':6',2''-三吡啶吡啶电子受体基团。在过渡金属离子的引导下,结构单元的自组装引发聚合反应,分别形成相应的金属-超分子聚合物PCzTPY,PSiTPY和PNTPY。构件的最大紫外可见吸收发生在长波长(CzTPY,SiTPY和NTPY分别为351、368和430 nm)处,这是由于分子内电荷转移(ICT)跃迁引起的。但是,其相应的金属超分子聚合物的吸收最大值明显发生了红移(PCzTPY,PSiTPY和PNTPY分别为394、431和509 nm),这是由于过渡金属离子掺入了靶标的主链而引起的。聚合物。基于上述策略,所得的金属聚合物显示出减小的能隙,对于PCzTPY,PSiTPY和PNTPY金属超分子聚合物,其能隙分别为2.07、1.97和1.56eV。 (C)2016 Elsevier Ltd.保留所有权利。

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