首页> 外文期刊>The Journal of Chemical Physics >Ultrafast transient absorption spectroscopy of the photodecarbonylation of photo-oxadibenzocyclooctyne (photo-ODIBO)
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Ultrafast transient absorption spectroscopy of the photodecarbonylation of photo-oxadibenzocyclooctyne (photo-ODIBO)

机译:光二苯苯并屈绝康锡(Photo-Odibo)光二羰基化的超快瞬态吸收光谱(Photo-Odibo)

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摘要

The ultrafast dynamics of photo-OxaDiBenzocycloOctyne (photo-ODIBO) photo-dissociation was studied using femtosecond transient absorption spectroscopy. Steady-state UV-Vis, time-dependent density functional theory, and 350 nm and 321 nm transient absorption studies are reported. Photo-ODIBO excitation with 321 nm and 350 nm light-induced photodecarbonylation of the cyclopropenone functional group results in the formation of ODIBO. The presence of the photoproduct was confirmed by the results of steady-state photolysis experiments and the observation of absorption signatures of ODIBO in the photo-ODIBO transient absorption spectra. Analysis of the latter revealed the underlying photochemical mechanisms and associated time constants, following excitation of the samples. The dynamics show a multi-exponential decay process, following the dissociation of photo-ODIBO into an excited state of the photoproduct ODIBO within <294 fs after 321 nm excitation. 350 nm excitation, on the other hand, is shown to produce ground state ODIBO via an intermediate species. Additional transient absorption measurements were performed directly on the photoproduct ODIBO to help distinguish spectral signatures associated with these processes.
机译:利用飞秒瞬态吸收光谱研究了光-恶二苯并环辛炔(photo-ODIBO)光离解的超快动力学。报道了稳态紫外-可见光谱、含时密度泛函理论、350nm和321nm瞬态吸收研究。在321nm和350nm光激发下,光诱导环丙烯酮官能团的光脱羰反应导致了ODIBO的形成。稳态光解实验的结果和在光ODIBO瞬态吸收光谱中观察到的ODIBO吸收特征证实了光产物的存在。对后者的分析揭示了激发样品后潜在的光化学机制和相关的时间常数。在321nm激发后<294fs内,光ODIBO分解为光产物ODIBO的激发态后,动力学表现出多指数衰减过程。另一方面,350 nm的激发通过中间物种产生基态ODIBO。直接在光产物ODIBO上进行额外的瞬态吸收测量,以帮助区分与这些过程相关的光谱特征。

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