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异双核钌-硼配合物中一种显著的陈-钌相互作用的热化学和分子结构。

Thermochemistry and molecular structure of a remarkable agostic interaction in a heterobifunctional ruthenium-boron complex.

机构信息

Loker Hydrocarbon Research Institute and Department of Chemistry, University of Southern California, Los Angeles, California 90089-1661, USA.

出版信息

J Am Chem Soc. 2010 Feb 17;132(6):1764-5. doi: 10.1021/ja909858a.

Abstract

A boron-pendant ruthenium species forms a unique agostic methyl bridge between the boron and ruthenium atoms in the presence of a ligating solvent, acetonitrile. NMR inversion-recovery experiments enabled the activation and equilibrium thermochemistry for formation of the agostic bridge to be measured. The mechanism for bridge formation involves displacement of an acetonitrile ligand; thus, this is a rare example of a case where an agostic C-H ligand competitively displaces another tightly binding ligand from a coordinatively saturated complex. Characterization of this complex gives unique insights into the development of C-H activation catalysis based on this ligand-metal bifunctional motif.

摘要

在配位溶剂乙腈存在的情况下,硼原子和钌原子之间形成了一个独特的桥连桥接甲基,其中含有一个硼原子。NMR 反转恢复实验使得桥接的形成的活化和平衡热化学得以被测量。桥形成的机制涉及乙腈配体的取代;因此,这是一个罕见的例子,其中一个桥接的 C-H 配体从配位饱和的配合物中竞争取代另一个紧密结合的配体。对这个配合物的特征分析为基于这种配体-金属双功能基序的 C-H 活化催化提供了独特的见解。

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