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首页> 外文期刊>The Journal of Chemical Physics >Photodissociation yield spectroscopy of vinyl bromide cation generated by mass-analyzed threshold ionization: Vibrational spectroscopy and decay dynamics in the (B)over-tilde state
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Photodissociation yield spectroscopy of vinyl bromide cation generated by mass-analyzed threshold ionization: Vibrational spectroscopy and decay dynamics in the (B)over-tilde state

机译:质谱分析阈值电离产生的乙烯基溴阳离子的光解离产率光谱:(B)倾斜状态下的振动光谱和衰减动力学

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摘要

A new technique [mass-analyzed threshold ionization (MATI)-photodissociation yield spectroscopy] to probe bound excited states of a cation was developed, which measures photodissociation yield of the cation generated by mass-analyzed threshold ionization. A vibrational spectrum of vinyl bromide cation in the B state was obtained using this technique. Optical resolution in the low vibrational energy range of the spectrum was far better than in conventional MATI spectra. The origin of the B state was found at 2.2578 +/- 0.0003 eV above the first ionization onset. Almost complete vibrational assignment was possible for peaks appearing in the spectrum. Analysis of time-of-flight profiles of C2H3+ product ion obtained with different laser polarization angles suggested that photoexcited vinyl bromide cation remained in the B state for several hundred picoseconds prior to internal conversion to the ground state and dissociation therein. (c) 2007 American Institute of Physics.
机译:开发了一种新技术[质谱分析阈值电离(MATI)-光解离产率谱],用于探测阳离子的束缚激发态,该技术可测量由质量分析的阈值电离产生的阳离子的光解离产率。使用该技术获得处于B状态的乙烯基溴阳离子的振动光谱。光谱的低振动能范围内的光学分辨率远优于常规MATI光谱。发现B态的起源在第一次电离开始之上2.2578 +/- 0.0003eV。频谱中出现的峰几乎可以完全振动分配。分析以不同的激光偏振角获得的C2H3 +产物离子的飞行时间分布曲线表明,光激发的乙烯基溴阳离子在内部转化为基态并解离之前,在B态保持了数百皮秒。 (c)2007年美国物理研究所。

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