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Cationic iridium complexes bearing imidazol-2-ylidene ligands as transfer hydrogenation catalysts

Anna C. Hillier, +2 more
- Vol. 222, Iss: 1
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TLDR
In this article, the synthesis and characterization of the PF6 and diazabutadienes complexes were reported. But their activity was not compared with that of the related cationic iridium(I) species.
Abstract
The synthesis and characterization by X-ray crystallography of the complexes [Ir(cod)(py)(L)]PF6 (L = IMes, 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (2); L = IPr, 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (3); L = ICy, 1,3-bis(cyclohexyl)imidazol-2-ylidene (4)) are reported. Complexes 2−4 have been employed as catalysts for transfer hydrogenation reactions from 2-propanol to a number of unsaturated substrates and their activity compared with that of the related cationic iridium(I) species [Ir(cod)(py)(SIMes)]PF6 (1), [Ir(cod)(py)(PCy3)]PF6 (5), and complexes formed in situ from [Ir(cod)(py)2]PF6 and diazabutadienes (RNCHCHNR, DAB-R; R = cyclohexyl, DAB-Cy; R = 2,4,6-trimethylphenyl, DAB-Mes; R = adamantyl, DAB-Ad; R = 2,4,6-trimethoxyphenyl, DAB-trimethoxyphenyl). All complexes tested were found to be active catalysts for transfer hydrogenation of ketones, with complex 4 displaying the highest activity. Complex 4 also exhibits moderate activity toward simple olefins and an aromatic nitro co...

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Citations
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N-heterocyclic carbenes: a new concept in organometallic catalysis.

TL;DR: N-Heterocyclic carbenes have become universal ligands in organometallic and inorganic coordination chemistry as mentioned in this paper, and they not only bind to any transition metal, be it in low or high oxidation states, but also to main group elements such as beryllium, sulfur, and iodine.
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Percent buried volume for phosphine and N-heterocyclic carbene ligands : steric properties in organometallic chemistry

TL;DR: This review presents the development of a more general method to determine the steric parameter of organometallic ligands and two case studies are presented: the tertiary phosphines and the N-heterocyclic carbenes.
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SambVca: A Web Application for the Calculation of the Buried Volume of N‐Heterocyclic Carbene Ligands

TL;DR: In this article, a free web application for the calculation of the buried volume of NHC ligands is presented, which provides a graphic and user-friendly interface to the SambVca program.
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Understanding the M(NHC) (NHC = N-heterocyclic carbene) bond

TL;DR: In this article, the authors provide an overview of the main contributions achieved by the application of advanced computational techniques in the N-heterocyclic carbenes (NHC) bond.
References
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Journal ArticleDOI

N-heterocyclic carbenes: a new concept in organometallic catalysis.

TL;DR: N-Heterocyclic carbenes have become universal ligands in organometallic and inorganic coordination chemistry as mentioned in this paper, and they not only bind to any transition metal, be it in low or high oxidation states, but also to main group elements such as beryllium, sulfur, and iodine.
Journal ArticleDOI

Percent buried volume for phosphine and N-heterocyclic carbene ligands : steric properties in organometallic chemistry

TL;DR: This review presents the development of a more general method to determine the steric parameter of organometallic ligands and two case studies are presented: the tertiary phosphines and the N-heterocyclic carbenes.
Journal ArticleDOI

SambVca: A Web Application for the Calculation of the Buried Volume of N‐Heterocyclic Carbene Ligands

TL;DR: In this article, a free web application for the calculation of the buried volume of NHC ligands is presented, which provides a graphic and user-friendly interface to the SambVca program.
Journal ArticleDOI

Understanding the M(NHC) (NHC = N-heterocyclic carbene) bond

TL;DR: In this article, the authors provide an overview of the main contributions achieved by the application of advanced computational techniques in the N-heterocyclic carbenes (NHC) bond.
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