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通过宽带微波光谱法测量皮秒异构化动力学。

Measuring picosecond isomerization kinetics via broadband microwave spectroscopy.

作者信息

Dian Brian C, Brown Gordon G, Douglass Kevin O, Pate Brooks H

机构信息

Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, VA 22904-4319, USA.

出版信息

Science. 2008 May 16;320(5878):924-8. doi: 10.1126/science.1155736.

Abstract

The rotational spectrum of a highly excited molecule is qualitatively different from its pure rotational spectrum and contains information about the intramolecular dynamics. We have developed a broadband Fourier transform microwave spectrometer that uses chirped-pulse excitation to measure a rotational spectrum in the 7.5- to 18.5-gigahertz range in a single shot and thereby reduces acquisition time sufficiently to couple molecular rotational spectroscopy with tunable laser excitation. After vibrationally exciting a single molecular conformation of cyclopropane carboxaldehyde above the barrier to C-C single-bond isomerization, we applied line-shape analysis of the dynamic rotational spectrum to reveal a product yield and picosecond reaction rate that were significantly different from statistical predictions. The technique should be widely applicable to dynamical studies of radical intermediates, molecular complexes, and conformationally flexible molecules with biological interest.

摘要

高激发分子的转动光谱在性质上不同于其纯转动光谱,并且包含有关分子内动力学的信息。我们开发了一种宽带傅里叶变换微波光谱仪,它使用啁啾脉冲激发来单次测量7.5至18.5千兆赫兹范围内的转动光谱,从而充分减少采集时间,以便将分子转动光谱与可调谐激光激发相结合。在将环丙烷甲醛的单个分子构象振动激发到高于C-C单键异构化的势垒后,我们对动态转动光谱进行线形分析,以揭示与统计预测有显著差异的产物产率和皮秒反应速率。该技术应广泛适用于自由基中间体、分子复合物以及具有生物学意义的构象灵活分子的动力学研究。

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