Suppr超能文献

区分通过芴低聚物进行分子内电荷转移的超交换和跳跃机制所面临的挑战。

Challenges in distinguishing superexchange and hopping mechanisms of intramolecular charge transfer through fluorene oligomers.

作者信息

Goldsmith Randall H, DeLeon Orlando, Wilson Thea M, Finkelstein-Shapiro Daniel, Ratner Mark A, Wasielewski Michael R

机构信息

Department of Chemistry, Argonne-Northwestern Solar Energy Research Center, and International Institute for Nanotechnology, Northwestern University, Evanston, Illinois 60208-3113, USA.

出版信息

J Phys Chem A. 2008 May 15;112(19):4410-4. doi: 10.1021/jp801084v. Epub 2008 Apr 18.

Abstract

The temperature dependence of intramolecular charge separation in a series of donor-bridge-acceptor molecules having phenothiazine (PTZ) donors, 2,7-oligofluorene FL(n) (n = 1-4) bridges, and perylene-3,4:9,10-bis(dicarboximide) (PDI) acceptors was studied. Photoexcitation of PDI to its lowest excited singlet state results in oxidation of PTZ via the FL(n) bridge. In toluene, the temperature dependence of the charge separation rate constants for PTZ-FL(n)-PDI, (n = 1-4) is relatively weak and is successfully described by the semiclassical Marcus equation. The activation energies for charge separation suggest that bridge charge carrier injection is not the rate limiting step. The difficulty of using temperature and length dependence to differentiate hopping and superexchange is discussed, with difficulties in the latter topic explored via an extension of a kinetic model proposed by Bixon and Jortner.

摘要

研究了一系列具有吩噻嗪(PTZ)供体、2,7-低聚芴FL(n)(n = 1 - 4)桥和苝-3,4:9,10-双(二甲酰亚胺)(PDI)受体的供体-桥-受体分子中分子内电荷分离的温度依赖性。PDI光激发到其最低激发单重态会通过FL(n)桥导致PTZ氧化。在甲苯中,PTZ-FL(n)-PDI(n = 1 - 4)电荷分离速率常数的温度依赖性相对较弱,并且可以通过半经典的马库斯方程成功描述。电荷分离的活化能表明桥电荷载流子注入不是速率限制步骤。讨论了利用温度和长度依赖性来区分跳跃和超交换的困难,并通过扩展Bixon和Jortner提出的动力学模型来探讨后一主题中的困难。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验