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一种不对称1,2-双(硅烯)稳定的五羰基铬(0)物种的分离及多样反应性

Isolation and Diverse Reactivity of an Unsymmetrical 1,2-Bis(silylene)-Stabilized Pentacarbonyl Chromium(0) Species.

作者信息

Fan Jiawei, Wang Yuyi, Shi Tao, Yang Peng, Zhou Guijiang, Xu Jian, Su Bochao

机构信息

School of Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an Key Laboratory of Sustainable Energy Materials Chemistry, Xi'an Jiaotong University, Xi'an 710049, China.

Zhangye Dagong Pesticide Chemistry Co., Ltd., Zhangye 734000, China.

出版信息

Inorg Chem. 2024 Sep 23;63(38):17469-17477. doi: 10.1021/acs.inorgchem.4c01803. Epub 2024 Sep 3.

Abstract

The construction of the unsymmetrical 1,2-bis(silylene) pentacarbonyl chromium(0) complex was achieved through the reaction of chlorosilylene with half an equivalent of KCr(CO). X-ray diffraction analysis of confirms the formation of the Si-Si bond and the coordination of one of the silicon atoms to the Cr center. Density functional theory (DFT) calculations disclose that highest occupied molecular orbital (HOMO) mainly corresponds to the lone pair of electrons on the silicon atom and the σ-bonding interaction between two Si atoms. Based on its unique electronic structure, its diverse reactivity toward the transition metal compounds and small molecules was investigated in detail. The reactions of with Fe(CO) or CuCl yielded the 1,2-bis(silylene)-stabilized heterobimetallic complex or oxidized product , respectively. Additionally, treatments of with selenium, CO, or MeSiN led to the formation of the corresponding selenium-, oxo-, and nitrogen-bridged complexes . All compounds were characterized by multinuclear NMR spectroscopy and X-ray crystallography.

摘要

通过氯硅烯与半当量的KCr(CO)反应,实现了不对称1,2 - 双(硅烯)五羰基铬(0)配合物的构建。对其进行X射线衍射分析证实了Si - Si键的形成以及其中一个硅原子与Cr中心的配位。密度泛函理论(DFT)计算表明,最高占据分子轨道(HOMO)主要对应于硅原子上的孤对电子以及两个Si原子之间的σ键相互作用。基于其独特的电子结构,详细研究了其对过渡金属化合物和小分子的多种反应活性。与Fe(CO)或CuCl反应分别生成了1,2 - 双(硅烯)稳定的异双金属配合物或氧化产物。此外,用硒、CO或MeSiN处理会导致形成相应的硒桥、氧桥和氮桥配合物。所有化合物均通过多核NMR光谱和X射线晶体学进行了表征。

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