Bull James N, West Christopher W, Verlet Jan R R
Department of Chemistry , Durham University , South Road , DH1 3LE , UK . Email:
Chem Sci. 2015 Feb 1;6(2):1578-1589. doi: 10.1039/c4sc03491k. Epub 2014 Dec 17.
Frequency-, angle-, and time-resolved photoelectron imaging of gas-phase menadione (vitamin K) radical anions was used to show that quasi-bound resonances of the anion can act as efficient doorway states to produce metastable ground electronic state anions on a sub-picosecond timescale. Several anion resonances have been experimentally observed and identified with the assistance of calculations, and ground state anion recovery was observed across the first 3 eV above threshold. Time-resolved measurements revealed the mechanism of electronic ground state anion formation, which first involves a cascade of very fast internal conversion processes to a bound electronic state that, in turn, decays by slower internal conversion to the ground state. Autodetachment processes from populated resonances are inefficient compared with electronic relaxation through internal conversion. The mechanistic understanding gained provides insight into the formation of radical anions in biological and astrochemical systems.
利用气相甲萘醌(维生素K)自由基阴离子的频率分辨、角度分辨和时间分辨光电子成像表明,阴离子的准束缚共振可以作为有效的门道态,在亚皮秒时间尺度上产生亚稳态基态电子态阴离子。借助计算实验观察并识别了几种阴离子共振,并且在高于阈值的首个3电子伏特范围内观察到了基态阴离子的恢复。时间分辨测量揭示了电子基态阴离子的形成机制,该机制首先涉及一系列非常快速的内转换过程,形成一个束缚电子态,该束缚电子态又通过较慢的内转换衰变为基态。与通过内转换进行的电子弛豫相比,从占据的共振态发生的自解离过程效率较低。所获得的机理理解为生物和天体化学系统中自由基阴离子的形成提供了见解。