Issue 4, 2022

The reaction of rhenium nitrosyl with a sterically hindered NHC-carbene

Abstract

In this article, we present the serendipitous synthesis of the unknown Re(I) complex [(OPPh3)Re(NO)2Cl3] (3) that we obtained reacting the Re(V) complex trans-[(PPh3)2ReOCl3] (1) with NO gas in presence of CH3COOH. We found that 3 reacts with 1,3-bis (2,4,6-trimethylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene (IMes) to yield a stable oximate—Re(III) complex [(OPPh3)Re(NO)(ON[double bond, length as m-dash]IMes)Cl3] (4). We speculate that the IMes reacts with a bent NO, because the DFT calculations excluded the formation of both dimeric and η2–NO complexes in solution. The reactivity of the NO toward the carbene is probably due to an internal fluxional process in which the NO passes from linear to bent, triggered by the π-electrons given by the three chlorides to the Re through the mesomeric effect.

Graphical abstract: The reaction of rhenium nitrosyl with a sterically hindered NHC-carbene

Supplementary files

Article information

Article type
Paper
Submitted
23 Nov 2021
Accepted
24 Dec 2021
First published
06 Jan 2022
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2022,51, 1521-1526

The reaction of rhenium nitrosyl with a sterically hindered NHC-carbene

G. Grieco and O. Blacque, Dalton Trans., 2022, 51, 1521 DOI: 10.1039/D1DT03966K

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