FEMTOSECOND TRANSIENT ABSORPTION STUDY OF THE RING-OPENING REACTION OF 1,3-CYCLOHEXADIENE

被引:68
作者
PULLEN, S
WALKER, LA
DONOVAN, B
SENSION, RJ
机构
[1] Department of Chemistry, University of Michigan, Ann Arbor
基金
美国国家科学基金会;
关键词
D O I
10.1016/0009-2614(95)00772-V
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
Deep ultraviolet femtosecond transient absorption measurements of the photoisomerization reaction of 1,3-cyclohexadiene to form cis-1,3,5-hexatriene demonstrate that the rate of the photochemical ring-opening reaction is greater than or equal to 1 ps(-1). The subsequent kinetics observed in picosecond resonance Raman and transient absorption measurements represent the time scales for vibrational and conformational relaxation of the photoproduct.
引用
收藏
页码:415 / 420
页数:6
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