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通过脉冲场电离电子能谱研究中性和阳离子双(苯)钛和钒夹心配合物的电子态。

Electronic states of neutral and cationic bis(benzene) titanium and vanadium sandwich complexes studied by pulsed field ionization electron spectroscopy.

作者信息

Sohnlein Bradford R, Lei Yuxiu, Yang Dong-Sheng

机构信息

Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506-0055, USA.

出版信息

J Chem Phys. 2007 Sep 21;127(11):114302. doi: 10.1063/1.2771158.

Abstract

Ti- and V-bz2 (bz=C6H6) sandwich complexes have been prepared in a laser-ablation cluster beam source and studied by pulsed field ionization-zero electron kinetic energy photoelectron spectroscopy and theoretical calculations. The ground electronic states of the neutral Ti- and V-bz2 complexes are determined to be 1A1g and 2A1g, and their ionization energies are measured to be 5.732+/-0.001 and 5.784+/-0.002 eV, respectively. These neutral complexes have eta6 binding and are in an eclipsed D6h configuration with flat benzene rings. Ionization of the 1A1g and 2A1g neutral states of Ti- and V-bz2 yields the 2B1g and 3B1g ion states, respectively, in a D2h point group with slightly puckered benzene rings. In addition, the binding and structures of these two complexes are compared with other first-row transition metal bis(benzene) sandwiches.

摘要

钛和钒的二苯并二茂夹心配合物(bz = C6H6)已在激光烧蚀团簇束源中制备,并通过脉冲场电离-零电子动能光电子能谱和理论计算进行了研究。中性钛和钒的二苯并二茂配合物的基态电子态分别确定为1A1g和2A1g,其电离能分别测量为5.732±0.001和5.784±0.002 eV。这些中性配合物具有η6键合,并且处于苯环扁平的重叠D6h构型。钛和钒的二苯并二茂配合物的1A1g和2A1g中性态的电离分别产生具有略微褶皱苯环的D2h点群中的2B1g和3B1g离子态。此外,将这两种配合物的键合和结构与其他第一行过渡金属双(苯)夹心配合物进行了比较。

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