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rac-顺式-二羰基-氯代{1-[2-(二苯基-膦基-κP)苄基]-3-(苯基-κC(1))咪唑-2-亚基-κC(2)}钌(II) 二氯甲烷单溶剂合物

rac-cis-Dicarbonyl-chlorido{1-[2-(diphenyl-phosphanyl-κP)benz-yl]-3-(phenyl-κC(1))imidazol-2-yl-idene-κC(2)}ruthenium(II) dichloro-methane monosolvate.

作者信息

Domski Gregory J, Pecak Wiktoria H, Swenson Dale C

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2012 Sep 1;68(Pt 9):m1224-5. doi: 10.1107/S1600536812036665. Epub 2012 Aug 31.

DOI:10.1107/S1600536812036665
PMID:22969503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3435630/
Abstract

In the title compound, [Ru(C(28)H(22)N(2)P)Cl(CO)(2)]·CH(2)Cl(2), the Ru(II) atom exhibits a distorted octa-hedral coordination geometry. The N-phenyl group of the ligand has undergone orthometalation; as a result, the tridentate phosphane-functionalized N-heterocyclic carbene ligand is coordinating in a meridional fashion. This complex is of inter-est with respect to transfer hydrogenation catalysis and also provides an example of C-H activation behavior in late transition metal complexes. The dichloro-methane solvent mol-ecule is disordered over two sets of sites with an occupancy ratio of 0.873 (14):0.127 (14).

摘要

在标题化合物[Ru(C₂₈H₂₂N₂P)Cl(CO)₂]·CH₂Cl₂中,Ru(II)原子呈现出扭曲的八面体配位几何构型。配体的N-苯基发生了邻位金属化;因此,三齿膦功能化的N-杂环卡宾配体以经式方式配位。该配合物在转移氢化催化方面具有重要意义,同时也为后过渡金属配合物中的C-H活化行为提供了一个实例。二氯甲烷溶剂分子在两组位置上无序分布,占有率为0.873 (14):0.127 (14)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c38/3435630/839e89cd0854/e-68-m1224-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c38/3435630/839e89cd0854/e-68-m1224-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c38/3435630/839e89cd0854/e-68-m1224-fig1.jpg

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