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Perspective: Bimolecular chemical reaction dynamics in liquids
被引:42
作者:
Orr-Ewing, Andrew J.
[1
]
机构:
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
基金:
英国科学技术设施理事会;
英国工程与自然科学研究理事会;
欧洲研究理事会;
关键词:
RESOLVED RESONANCE RAMAN;
CN RADICAL REACTIONS;
MOLECULAR REACTION DYNAMICS;
ROOM-TEMPERATURE LIQUIDS;
BOND-SPECIFIC CHEMISTRY;
SOLUTION-PHASE;
ULTRAVIOLET PHOTOLYSIS;
CHLORINE-ATOM;
PHOTOISOMERIZATION REACTION;
INFRARED-SPECTROSCOPY;
D O I:
10.1063/1.4866761
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:
Bimolecular reactions in the gas phase exhibit rich and varied dynamical behaviour, but whether a profound knowledge of the mechanisms of isolated reactive collisions can usefully inform our understanding of reactions in liquid solutions remains an open question. The fluctuating environment in a liquid may significantly alter the motions of the reacting particles and the flow of energy into the reaction products after a transition state has been crossed. Recent experimental and computational studies of exothermic reactions of CN radicals with organic molecules indicate that many features of the gas-phase dynamics are retained in solution. However, observed differences may also provide information on the ways in which a solvent modifies fundamental chemical mechanisms. This perspective examines progress in the use of time-resolved infra-red spectroscopy to study reaction dynamics in liquids, discusses how existing theories can guide the interpretation of experimental data, and suggests future challenges for this field of research. (C) 2014 AIP Publishing LLC.
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页数:12
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