STATE-TO-STATE MEASUREMENTS OF INTERNAL ROTATIONAL PREDISSOCIATION IN OH-AR (A(2)SIGMA(+))

被引:19
作者
GIANCARLO, LC
RANDALL, RW
CHOI, SE
LESTER, MI
机构
[1] Department of Chemistry, University of Pennsylvania, Philadelphia
[2] Physical Chemistry Laboratory, Oxford University, Oxford OX13QZ, South Parks Road
关键词
D O I
10.1063/1.467604
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
Internal rotational predissociative levels of OH-Ar (A (2) Sigma(+)) have been identified lying up to 350 cm(-1) above the OH A (2) Sigma(+) (v = 0, 1)+Ar dissociation limit. The predissociative level energies, lifetimes, and OH A (2) Sigma(+) rotational product distributions have been measured. Complexes prepared in many of these predissociative levels are long lived with lifetimes greater than or equal to 50 ps. A novel variation of stimulated emission pumping has enabled quantitative OH A (2) Sigma(+) rotational distributions to be obtained following OH-Ar predissociation. The OH product distributions are highly selective. The highest energetically available channel is always populated, yet in many cases, low rotational levels are conspicuously absent. The OH-Ar predissociative levels have been assigned nearly good quantum numbers based on a rotational contour analysis of the predissociative features and/or the OH A (2) Sigma(+) rotational product distributions. A two-step mechanism involving Coriolis coupling and the potential anisotropy has been proposed to describe the predissociation process. A comparison between the experimentally measured and theoretically calculated observables provides a guide for further refinements of the OH A (2) Sigma(+) +Ar potential energy surface.
引用
收藏
页码:2914 / 2928
页数:15
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