Photodissociation of dimethyl sulfide at 227.5 nm:: resonance-enhanced multiphoton ionization of the methyl fragment

被引:17
|
作者
Martínez-Haya, B
Zapater, I
Quintana, P
Menéndez, M
Verdasco, E
Santamaría, J
Bañares, L
Aoiz, FJ [1 ]
机构
[1] Univ Complutense, Fac Quim, Dept Quim Fis 1, E-28040 Madrid, Spain
[2] Univ Complutense, Fac Quim, CAI Espectroscopia, E-28040 Madrid, Spain
关键词
D O I
10.1016/S0009-2614(99)00855-6
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 photodissociation of CH3-S-CH3 following the lowest dipole-allowed transition 1 B-1(1)(9a(1) <-- 3b(1)) <-- X(1)A(1) has been studied. The CH, photofragment has been detected by 2 + 1 resonance-enhanced multiphoton ionization through the 3p(z)(2)A "(2) <-- X(2)A "(2) and 4p(z) (2)A "(2) <-- X(2)A "(2) Rydberg transitions. The vibronic spectrum corresponding to the nu(2) ,'umbrella' mode of CH3 has been measured and fragments with nu(2) = 0 to nu(2) = 4 quanta of vibrational excitation have been detected. From the analysis of the 4p(z) rotationally resolved 0(0)(0) band of CH3, rotational temperatures T-N= 325 +/- 75 K and T-K= 125 +/- 50 K have been obtained for the ground vibrational state of the nascent CH, fragment. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:159 / 166
页数:8
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