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Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand

[Image: see text] Iridium(I) complexes of the type IrX(olefin)(α-diimine) (α-diimine = 1,4-bis(2,6-xylyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; X = Cl, I, Me, O(2)CCF(3); olefin = ethylene, cyclooctene (COE)) were synthesized from the readily available precursor [IrCl(COE)(2)](2). These complexes di...

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Autores principales: Kovach, James, Golisz, Suzanne R., Brennessel, William W., Jones, William D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710518/
https://www.ncbi.nlm.nih.gov/pubmed/36466792
http://dx.doi.org/10.1021/acs.organomet.2c00036
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author Kovach, James
Golisz, Suzanne R.
Brennessel, William W.
Jones, William D.
author_facet Kovach, James
Golisz, Suzanne R.
Brennessel, William W.
Jones, William D.
author_sort Kovach, James
collection PubMed
description [Image: see text] Iridium(I) complexes of the type IrX(olefin)(α-diimine) (α-diimine = 1,4-bis(2,6-xylyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; X = Cl, I, Me, O(2)CCF(3); olefin = ethylene, cyclooctene (COE)) were synthesized from the readily available precursor [IrCl(COE)(2)](2). These complexes display unusual (1)H NMR spectra and have large UV–vis extinction coefficients. NOESY and HSQC NMR experiments were used to provide rigorous NMR spectral assignments, and IrCl(C(2)H(4))(α-diimine), 1, and IrCl(COE)(α-diimine), 4, were structurally characterized by X-ray crystallography. The related rhodium complex [RhCl(α-diimine)](2), 6, was also synthesized and characterized by NMR and X-ray crystallography. 6 was observed to be in equilibrium with RhCl(C(2)H(4))(α-diimine), 7, under an ethylene atmosphere.
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spelling pubmed-97105182022-12-01 Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand Kovach, James Golisz, Suzanne R. Brennessel, William W. Jones, William D. Organometallics [Image: see text] Iridium(I) complexes of the type IrX(olefin)(α-diimine) (α-diimine = 1,4-bis(2,6-xylyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; X = Cl, I, Me, O(2)CCF(3); olefin = ethylene, cyclooctene (COE)) were synthesized from the readily available precursor [IrCl(COE)(2)](2). These complexes display unusual (1)H NMR spectra and have large UV–vis extinction coefficients. NOESY and HSQC NMR experiments were used to provide rigorous NMR spectral assignments, and IrCl(C(2)H(4))(α-diimine), 1, and IrCl(COE)(α-diimine), 4, were structurally characterized by X-ray crystallography. The related rhodium complex [RhCl(α-diimine)](2), 6, was also synthesized and characterized by NMR and X-ray crystallography. 6 was observed to be in equilibrium with RhCl(C(2)H(4))(α-diimine), 7, under an ethylene atmosphere. American Chemical Society 2022-04-05 2022-11-28 /pmc/articles/PMC9710518/ /pubmed/36466792 http://dx.doi.org/10.1021/acs.organomet.2c00036 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Kovach, James
Golisz, Suzanne R.
Brennessel, William W.
Jones, William D.
Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand
title Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand
title_full Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand
title_fullStr Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand
title_full_unstemmed Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand
title_short Iridium(I)– and Rhodium(I)–Olefin Complexes Containing an α-Diimine Supporting Ligand
title_sort iridium(i)– and rhodium(i)–olefin complexes containing an α-diimine supporting ligand
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710518/
https://www.ncbi.nlm.nih.gov/pubmed/36466792
http://dx.doi.org/10.1021/acs.organomet.2c00036
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