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Femtosecond relaxation of photoexcited p-nitroaniline in water: solvation, internal conversion and cooling

机译:飞秒光激发对硝基苯胺在水中的弛豫:溶剂化,内部转化和冷却

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Summary form only given. Para-nitroaniline (PNA) is the smallest organic molecule which exhibits strong photoexcited electron transfer from the NH/sub 2/ group to the NO/sub 2/ group. This charge transfer results in pronounced solvatochromic and nonlinear optical molecular properties. Therefore this molecule is of great interest both for chemists and engineers developing new nonlinear optical materials. However the photophysics of PNA is not fully understood yet. For example, fluorescence has not been observed due to very fast quenching processes in the first excited electronic state. Even a recent subpicosecond study, failed to detect the earliest (before 300 fs) spectral evolution. We observe for the first time and in spectroscopic detail all early stages of relaxation of PNA in water, by measuring transient absorption spectra with the pump-supercontinuum probe technique, after excitation at 400 nm with 50 fs pulses. The transient spectra are recorded in the range 300-700 nm with 20 fs time resolution.
机译:仅提供摘要表格。对硝基苯胺(PNA)是最小的有机分子,显示出从NH / sub 2 /基团到NO / sub 2 /基团的强光激发电子转移。这种电荷转移导致明显的溶剂变色和非线性光学分子性质。因此,该分子对于化学家和开发新的非线性光学材料的工程师都非常感兴趣。但是,对PNA的光物理还没有完全了解。例如,由于在第一激发电子状态下非常快速的淬灭过程,未观察到荧光。即使是最近的亚皮秒研究,也未能检测到最早的频谱演化(在300 fs之前)。我们首次观察到PNA在水中弛豫的所有早期阶段,并用光谱学的细节进行了观察,方法是用泵浦超连续谱探针技术测量瞬态吸收光谱,然后在50 nm脉冲下激发400 nm。瞬态光谱以20 fs的时间分辨率记录在300-700 nm范围内。

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