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里德堡态介导的(η-CH)(η-CH)Cr多光子电离:密度泛函理论支持的对激发夹心配合物分子和电子结构的实验见解

Rydberg state mediated multiphoton ionization of (η-CH)(η-CH)Cr: DFT-supported experimental insights into the molecular and electronic structures of excited sandwich complexes.

作者信息

Ketkov Sergey Yu, Tzeng Sheng Yuan, Rychagova Elena A, Kalakutskaya Lyubov' V, Fuss Marco, Braunschweig Holger, Tzeng Wen-Bih

机构信息

G. A. Razuvaev Institute of Organometallic Chemistry RAS, NIzhny Novgorod 603950, Russian Federation.

出版信息

Phys Chem Chem Phys. 2019 May 15;21(19):9665-9671. doi: 10.1039/c9cp00888h.

Abstract

The resonance-enhanced multiphoton ionization (REMPI) of a mixed sandwich complex has been achieved for the first time when exciting (η7-C7H7)(η5-C5H5)Cr via the Rydberg 4pz state. The REMPI spectrum is indicative of unexpectedly small changes of the sandwich geometry on excitation. Time-dependent DFT calculations reveal fine effects of the ligand nature on the molecular and electronic structure variations accompanying electronic excitation. Different trends are predicted for the sandwich geometry transformations in the mixed sandwich complex and its symmetric isomer, (η6-C6H6)2Cr, both on Rydberg excitation and ionization.

摘要

当通过里德堡4pz态激发(η7-C7H7)(η5-C5H5)Cr时,首次实现了混合夹心配合物的共振增强多光子电离(REMPI)。REMPI光谱表明,激发时夹心结构的变化出乎意料地小。含时密度泛函理论计算揭示了配体性质对伴随电子激发的分子和电子结构变化的精细影响。对于混合夹心配合物及其对称异构体(η6-C6H6)2Cr,在里德堡激发和电离时,夹心结构转变的趋势不同。

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