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有机钛配合物的金属和配体K边X射线吸收光谱:金属4p和3d对边前强度的贡献及其对成键的贡献。

Metal and ligand K-edge XAS of organotitanium complexes: metal 4p and 3d contributions to pre-edge intensity and their contributions to bonding.

作者信息

George Serena DeBeer, Brant Patrick, Solomon Edward I

机构信息

Stanford Synchrotron Radiation Laboratory, SLAC, Stanford University, Stanford, California 94309, USA.

出版信息

J Am Chem Soc. 2005 Jan 19;127(2):667-74. doi: 10.1021/ja044827v.

Abstract

Titanium cyclopentadienyl (Cp) complexes play important roles as homogeneous polymerization catalysts and have recently received attention as potential anticancer agents. To systematically probe the contribution of the Cp to bonding in organotitanium complexes, Ti K-edge XAS has been applied to TiCl(4) and then to the mono- and bis-Cp complexes, TiCpCl(3) and TiCp(2)Cl(2). Ti K-edge XAS is used as a direct probe of metal 3d-4p mixing and provides insight into the contribution of the Cp to bonding. These data are complimented by Cl K-edge XAS data, which provide a direct probe of the effect of the Cp on the bonding to the spectator chloride ligand. The experimental results are correlated to DFT calculations. A model for metal 3d-4p mixing is proposed, which is based on covalent interactions with the ligands and demonstrates that metal K-pre-edge intensities may be used as a measure of ligand-metal covalency in molecular Ti(IV) systems in noncentrosymmetric environments.

摘要

钛茂(Cp)配合物作为均相聚合催化剂发挥着重要作用,并且最近作为潜在的抗癌剂受到关注。为了系统地探究Cp对有机钛配合物中键合的贡献,Ti K边X射线吸收光谱(XAS)已应用于TiCl(4),然后应用于单茂和双茂配合物TiCpCl(3)和TiCp(2)Cl(2)。Ti K边XAS用作金属3d - 4p混合的直接探针,并深入了解Cp对键合的贡献。这些数据得到了Cl K边XAS数据的补充,后者提供了Cp对与旁观氯配体键合影响的直接探针。实验结果与密度泛函理论(DFT)计算相关。提出了一种基于与配体共价相互作用的金属3d - 4p混合模型,该模型表明金属K边前峰强度可用于衡量非中心对称环境中分子Ti(IV)体系中配体 - 金属的共价性。

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