Photochemistry and Photophysics at Extended Seams of Conical Intersection

被引:68
作者
Blancafort, Lluis [1 ,2 ]
机构
[1] Univ Girona, Inst Quim Computac & Catalisi, Campus Montilivi, Girona 17071, Spain
[2] Univ Girona, Dept Quim, Girona 17071, Spain
关键词
extended seams; isomerization; photochemistry; photophysics; reaction mechanisms; EXCITED-STATE DYNAMICS; POTENTIAL-ENERGY SURFACES; INITIO MOLECULAR-DYNAMICS; DENSITY-FUNCTIONAL THEORY; INTRAMOLECULAR PROTON-TRANSFER; AGGREGATION-INDUCED EMISSION; AB-INITIO; NONADIABATIC DYNAMICS; STARK CONTROL; WOLFF-REARRANGEMENT;
D O I
10.1002/cphc.201402359
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 role of extended seams of conical intersection in excited-state mechanisms is reviewed. Seams are crossings of the potential energy surface in many dimensions where the decay from the excited to the ground state can occur, and the extended seam is composed of different segments lying along a reaction coordinate. Every segment is associated with a different primary photoproduct, which gives rise to competing pathways. This idea is first illustrated for fulvene and ethylene, and then it is used to explain more complex cases such as the dependence of the isomerisation of retinal chromophore isomers on the protein environment, the dependence of the efficiency of the azobenzene photochemical switch on the wavelength of irradiation and the direction of the isomerisation, and the coexistence of different mechanisms in the photo-induced Wolff rearrangement of diazonaphthoquinone. The role of extended seams in the photophysics of the DNA nucleobases and the relationship between two-state seams and three-state crossings is also discussed. As an outlook, the design of optical control strategies based on the passage of the excited molecule through the seam is considered, and it is shown how the excited-state lifetime of fulvene can be modulated by shaping the energy of the seam.
引用
收藏
页码:3166 / 3181
页数:16
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