A Tour in the Chemistry of a Tricoordinate Rh(-I) Complex.

Chemistry

Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH) CSIC-Universidad de Zaragoza, Pedro Cerbuna 12, Facultad de Ciencias, Zaragoza, 50009, Spain.

Published: July 2025


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Article Abstract

The finding of the unprecedented 16-e tricoordinate planar rhodium(-Ι) complex, K[Rh(IPr)(dvtms)] (K[1]) (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazolyl-2-ylidene, dvtms = divinyltretramethyldisiloxane) prompted us to explore its reactivity. K[1] reacts as a nucleophile with methyliodide to give [Rh(IPr)(dvtms)Me], a Rh(Ι) compound with an exceptional trigonal-pyramidal structure. Other haloalkanes abstract one electron from K[1] to give the previously reported [Rh(IPr)(dvtms)] complex. K[1] also reacts with protonic acids and weak proton sources such as water and ketones to eventually give the rare tricoordinate 14-electron complex [Rh(IPr)(SiMeOSiMeCH = CH)] with a Rh -Si bond. The 16-electron complex [Rh(IPr)(SiMeOSiMeCH = CH)(HC = CH)] was characterized as an intermediate in this reaction. Furthermore, K[1] runs up to five cycles of catalytic condensation of nonenolizable aldehydes to esters, such as p-tolylaldehyde, before being fully converted into the inactive complex Rh(IPr)(η-CH tolyl)(CH)] with fragmentation of the diolefin dvtms. Computational studies have provided valuable insights into the reactivity patterns and behavior of this complex, including those of the rhodium(-I)/rhodium(I) catalytic cycle.

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http://dx.doi.org/10.1002/chem.202501877DOI Listing

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