光子上转换
光化学
胸腺嘧啶
激发态
飞秒
尿嘧啶
乙腈
荧光
单重态
化学
超快激光光谱学
内部转换
系统间交叉
基态
激发
三重态
单重态裂变
分子
量子产额
光激发
含时密度泛函理论
分子内力
皮秒
圆锥交点
电子转移
发光
材料科学
光电子学
物理
原子物理学
光学
有机化学
DNA
激光器
生物化学
作者
T. Gustavsson,Nilmoni Sarkar,E. Lazzarotto,Dimitra Markovitsi,Roberto Improta
标识
DOI:10.1016/j.cplett.2006.08.058
摘要
The excited state properties of uracil, thymine and four analogous uracil compounds have been studied in acetonitrile by steady-state and time-resolved spectroscopy. The excited state lifetimes were measured using femtosecond UV fluorescence upconversion. The excited state lifetimes of uracil and its 1- and 3-methyl substituted derivatives are well described by one ultrafast (⩽100 fs) component. Five substituted compounds show a more complex behavior, exhibiting longer excited state lifetimes and bi-exponential fluorescence decays. These longer decays are substantially faster in acetonitrile than in aqueous solution showing that the excited state deactivation mechanism is in part governed by the solvent.
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