The (A)over-tilde←(X)over-tilde (1+1) resonance-enhanced multiphoton ionization spectrum of the NO•C2H6 and NO•(C2H6)2 complexes

被引:16
作者
Daire, SE [1 ]
Lozeille, J [1 ]
Gamblin, SD [1 ]
Wright, TG [1 ]
机构
[1] Univ Sussex, Sch Chem Phys & Environm Sci, Brighton BN1 9QJ, E Sussex, England
关键词
D O I
10.1021/jp001858d
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 (A) over tilde <-- <(X)over tilde> transitions of NO .C2H6 and NO bullet>(*) over bar * (C2H6)(2) have been recorded using (1 + 1) resonance-enhanced multiphoton ionization spectroscopy. The NO .C2H6 origin is determined to be 44050 +/- 15 cm(-1), and the dissociation energy, D-0', of the (A) over tilde state is measured to be 340 +/- 20 cm(-1). The latter values allow the dissociation energy of the (X) over tilde state, D-0", to be determined as 190 +/- 20 cm(-1). In addition, estimates of the dissociation energies for the processes NO bullet>(*) over bar * (C2H6)(2) + NO .C2H6 + C2H6 and NO bullet>(*) over bar * (C2H6)(2) --> NO + 2C(2)H(6) in the (X) over tilde and (A) over tilde states are obtained; the (A) over tilde state is found to be dissociative along the NO .C2H6. . .C2H6 coordinate. Comparison of the NO .C2H6 (A) over tilde <-- <(X)over tilde> spectrum with that of NO . CH4 is made.
引用
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页码:9180 / 9183
页数:4
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