首页> 外文期刊>Chemistry: A European journal >Control over Excited State Intramolecular Proton Transfer and Photoinduced Tautomerization: Influence of the Hydrogen-Bond Geometry
【24h】

Control over Excited State Intramolecular Proton Transfer and Photoinduced Tautomerization: Influence of the Hydrogen-Bond Geometry

机译:激发态分子内质子转移和光致互变异构的控制:氢键几何的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

The influence of H-bond geometry on the dynamics of excited state intramolecular proton transfer (ESIPT) and photoinduced tautomerization in a series of phenol-quinoline compounds is investigated. Control over the proton donor-acceptor distance (d(DA)) and dihedral angle between the proton donor-acceptor subunits is achieved by introducing methylene backbone straps of increasing lengths to link the phenol and quinoline. We demonstrate that a long d(DA) correlates with a higher barrier for ESIPT, while a large dihedral angle opens highly efficient deactivation channels after ESIPT, preventing the formation of the fully relaxed tautomer photoproduct.
机译:研究了氢键几何结构对一系列酚-喹啉化合物的激发态分子内质子转移(ESIPT)和光致互变异构动力学的影响。质子供体-受体距离(d(DA))和质子供体-受体亚基之间的二面角的控制是通过引入长度增加的亚甲基骨架带连接苯酚和喹啉来实现的。我们证明,较长的d(DA)与ESIPT的较高壁垒相关,而较大的二面角在ESIPT之后打开了高效的失活通道,从而阻止了完全松弛的互变异构体光产物的形成。

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