分子内力
光激发
溶剂变色
电荷(物理)
光化学
偶极子
激发态
接受者
化学物理
化学
基态
材料科学
分子物理学
光电子学
原子物理学
物理
分子
立体化学
有机化学
凝聚态物理
量子力学
作者
Mengyao Hao,Weijie Chi,Chao Wang,Zhaochao Xu,Ze‐Sheng Li,Xiaogang Liu
标识
DOI:10.1021/acs.jpcc.0c04218
摘要
Intramolecular charge transfer (ICT) is a fundamental process in photochemistry, during which charge flows from a donor (D) to an acceptor (A). In (probably) most dyes, ICT is enhanced upon photoexcitation (namely, forward ICT or FICT), endowing these compounds with positive solvatochromism. Yet, many dyes display negative solvatochromism, suggesting backward ICT (BICT). That is, a significant charge separation from D to A is achieved in the ground state, but charge transports back from A to D upon photoexcitation, leading to a reduced dipole moment in the excited state. In contrast to the well-studied FICT systems, molecular design guidelines to realize BICT remain elusive, precluding potential applications. In this paper, we showed that BICT could be achieved by incorporating double donors and double acceptors with a quinoid π-bridge. The establishment of the BICT design rules not only deepens our understanding of charge transfer but also inspires future applications (i.e., nonlinear optics).
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