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镍的等结构一氧化二氮和二氧化碳配合物中的侧基配位

Side-on Coordination in Isostructural Nitrous Oxide and Carbon Dioxide Complexes of Nickel.

作者信息

Puerta Lombardi Braulio M, Gendy Chris, Gelfand Benjamin S, Bernard Guy M, Wasylishen Roderick E, Tuononen Heikki M, Roesler Roland

机构信息

Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB, T2N 1N4, Canada.

Department of Chemistry, Nanoscience Centre, University of Jyväskylä, P.O. Box 35, FI-40014, Jyväskylä, Finland.

出版信息

Angew Chem Int Ed Engl. 2021 Mar 22;60(13):7077-7081. doi: 10.1002/anie.202011301. Epub 2021 Feb 17.

Abstract

A nickel complex incorporating an N O ligand with a rare η -N,N'-coordination mode was isolated and characterized by X-ray crystallography, as well as by IR and solid-state NMR spectroscopy augmented by N-labeling experiments. The isoelectronic nickel CO complex reported for comparison features a very similar solid-state structure. Computational studies revealed that η -N O binds to nickel slightly stronger than η -CO in this case, and comparably to or slightly stronger than η -CO to transition metals in general. Comparable transition-state energies for the formation of isomeric η -N,N'- and η -N,O-complexes, and a negligible activation barrier for the decomposition of the latter likely account for the limited stability of the N O complex.

摘要

分离得到了一种包含具有罕见η-N,N'-配位模式的NO配体的镍配合物,并通过X射线晶体学以及通过N标记实验增强的红外光谱和固态核磁共振光谱对其进行了表征。报道用于比较的等电子镍羰基配合物具有非常相似的固态结构。计算研究表明,在这种情况下,η-NO与镍的结合比η-CO略强,并且与过渡金属的η-CO相比总体上相当或略强。异构η-N,N'-和η-N,O-配合物形成的可比过渡态能量,以及后者分解的可忽略不计的活化能垒可能是导致NO配合物稳定性有限的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf0f/8048599/927874b27c0e/ANIE-60-7077-g003.jpg

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