Theoretische Chemie, Fakultät für Chemie, Universität Bielefeld, Universitätsstr. 25, 33615 Bielefeld (Germany).
Angew Chem Int Ed Engl. 2014 Jan 20;53(4):1122-6. doi: 10.1002/anie.201307822. Epub 2013 Dec 4.
Extending the fully quantum-state-resolved description of elementary chemical reactions beyond three or four atom systems is a crucial issue in fundamental chemical research. Reactions of methane with F, Cl, H or O are key examples that have been studied prominently. In particular, reactive resonances and nonintuitive mode-selective chemistry have been reported in experimental studies for the F+CH4 →HF+CH3 reaction. By investigating this reaction using transition-state spectroscopy, this joint theoretical and experimental study provides a clear picture of resonances in the F+CH4 system. This picture is deduced from high-resolution slow electron velocity-map imaging (SEVI) spectra and accurate full-dimensional (12D) quantum dynamics simulations in the picosecond regime.
将基本化学反应的全量子态分辨描述扩展到三四个原子系统之外,是基础化学研究中的一个关键问题。甲烷与 F、Cl、H 或 O 的反应是研究得最为突出的典型例子。特别是,在 F+CH4→HF+CH3 反应的实验研究中已经报道了反应共振和非直观的模态选择化学。通过使用过渡态光谱学研究这个反应,这项理论与实验的联合研究提供了 F+CH4 体系中共振的清晰图像。这个图像是从皮秒范围内的高分辨率慢电子速度映射成像(SEVI)光谱和精确的全维(12D)量子动力学模拟中推断出来的。