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Ultrafast Elementary Photochemical Processes of Organic Molecules in Liquid Solution
被引:371
作者:
Kumpulainen, Tatu
[1
]
Lang, Bernhard
[1
]
Rosspeintner, Amulf
[1
]
Vauthey, Eric
[1
]
机构:
[1] Univ Geneva, Dept Phys Chem Sci 2, 30 Quai Ernest Ansermet, CH-1211 Geneva 4, Switzerland
基金:
瑞士国家科学基金会;
关键词:
EXCITED-STATE PROTON;
PHOTOINDUCED ELECTRON-TRANSFER;
INTRAMOLECULAR-CHARGE-TRANSFER;
TIME-RESOLVED FLUORESCENCE;
RING-OPENING REACTION;
PICOSECOND LASER PHOTOLYSIS;
ENERGY-GAP DEPENDENCE;
EXCITATION WAVELENGTH DEPENDENCE;
DIFFUSION-CONTROLLED REACTIONS;
CIS-TRANS PHOTOISOMERIZATION;
D O I:
10.1021/acs.chemrev.6b00491
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Ultrafast photochemical reactions in liquids occur on similar or shorter time scales compared to the equilibration of the optically populated excited state: This equilibration involves the relaxation of intramolecular and/or solvent modes.-As-a consequence, the reaction dynamics are no longer exponential, cannot be quantified by rate constants, and-may depend on the excitation wavelength contrary to slower photochemical processes occurring from equilibrated excited states. Such ultrafast photoinduced reactions do no longer obey the Kasha-Vavilov rule. Nonequilibrium effects are also observed:in diffusion-controlled intermolecular processes directly after photoexcitation and their proper description gives. access to the intrinsic reaction dynamics that are normally hidden by diffusion. Here we discuss these topics in relation to ultrafast: organic photochemical reactions in homogeneous-liquids. Discussed reactions include intra- and intermolecular electron- and proton-transfer processes, as well as photochromic reactions-occurring with and without bond breaking or bond formation, namely ring-opening reactions and cis-trans isomerizations, respectively.
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页码:10826 / 10939
页数:114
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