Ultrafast formation of I2 following 350-nm photodissociation of CF2I2 in n-hexane

被引:26
作者
El-Khoury, Patrick Z. [1 ,2 ]
Tarnovsky, Alexander N. [1 ,2 ]
机构
[1] Bowling Green State Univ, Dept Chem, Bowling Green, OH 43403 USA
[2] Bowling Green State Univ, Ctr Photochem Sci, Bowling Green, OH 43403 USA
关键词
D O I
10.1016/j.cplett.2007.12.081
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 [物理化学]; 081704 [应用化学];
摘要
This study presents the photodissociation dynamics of difluorodiiodomethane (CF2I2) in n-hexane by femtosecond pump-probe spectroscopy. Following 350-nm excitation of CF2I2 into the lowest-lying excited electronic state, the transient absorption spectra are measured between 355 and 785 nm up to a time delay of 1200 ps. The results suggest that electronically excited CF2I2* molecules undergo a step-wise decay giving rise to two iodine fragments. The majority of the nascent iodine fragments combine on a 2-ps timescale to form molecular iodine. The spectral evolution is complete within 500 ps where the quantum yield of I-2 formation is measured to be 32%. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:160 / 166
页数:7
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