Establishing new mechanisms with triplet and singlet excited-state hydrogen bonding roles in photoinduced liquid dynamics

被引:63
作者
Chu, Tian-shu [1 ,2 ,3 ]
Liu, Bai-tong [1 ,2 ,3 ]
机构
[1] Qingdao Univ, Growing Base State Key Lab, Lab New Fiber Mat & Modern Text, Inst Computat Sci & Engn, Qingdao 266071, Peoples R China
[2] Qingdao Univ, Coll Chem Sci & Engn, Coll Phys, Qingdao 266071, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
excited-state hydrogen bonding; photosensitized synthesis; fluorescence emission; hydrogen-atom abstracting reaction; rotational reorientation; excited-state proton transfer coupled with twisted intramolecular charge transfer; INTRAMOLECULAR CHARGE-TRANSFER; GAUSSIAN-BASIS SETS; ROTATIONAL REORIENTATION DYNAMICS; DENSITY-FUNCTIONAL THEORY; SENSING MECHANISM; PROTON-TRANSFER; ELECTRON-TRANSFER; DYE MOLECULES; TD-DFT; ULTRAFAST DYNAMICS;
D O I
10.1080/0144235X.2016.1148450
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interaction between hydrogen donor and acceptor molecules, known well as hydrogen bonding, forms a ubiquitous network in the natural and synthesis world. The hydrogen bonding role has thus been the subject of intensive work in the past. In this article, we discuss and show how the new mechanisms have been established in terms of the hydrogen bonding changes by reviewing some of the combined experimental and theoretical studies that have recently shed light on the intricate role of both triplet and singlet excited-state hydrogen bondings in photoinduced liquid dynamics and phenomena.
引用
收藏
页码:187 / 208
页数:22
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