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Reactivity of Gold Hydrides: O(2) Insertion into the Au–H Bond
[Image: see text] Dioxygen reacts with the gold(I) hydride (IPr)AuH under insertion to give the hydroperoxide (IPr)AuOOH, a long-postulated reaction in gold catalysis and the first demonstration of O(2) activation by Au–H in a well-defined system. Subsequent condensation gave the peroxide (IPr)Au–OO...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482408/ https://www.ncbi.nlm.nih.gov/pubmed/26146435 http://dx.doi.org/10.1021/om501165z |
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author | Roşca, Dragoş-Adrian Fernandez-Cestau, Julio Hughes, David L. Bochmann, Manfred |
author_facet | Roşca, Dragoş-Adrian Fernandez-Cestau, Julio Hughes, David L. Bochmann, Manfred |
author_sort | Roşca, Dragoş-Adrian |
collection | PubMed |
description | [Image: see text] Dioxygen reacts with the gold(I) hydride (IPr)AuH under insertion to give the hydroperoxide (IPr)AuOOH, a long-postulated reaction in gold catalysis and the first demonstration of O(2) activation by Au–H in a well-defined system. Subsequent condensation gave the peroxide (IPr)Au–OO–Au(IPr) (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene). The reaction kinetics are reported, as well as the reactivity of Au(I) hydrides with radical scavengers. |
format | Online Article Text |
id | pubmed-4482408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44824082015-12-18 Reactivity of Gold Hydrides: O(2) Insertion into the Au–H Bond Roşca, Dragoş-Adrian Fernandez-Cestau, Julio Hughes, David L. Bochmann, Manfred Organometallics [Image: see text] Dioxygen reacts with the gold(I) hydride (IPr)AuH under insertion to give the hydroperoxide (IPr)AuOOH, a long-postulated reaction in gold catalysis and the first demonstration of O(2) activation by Au–H in a well-defined system. Subsequent condensation gave the peroxide (IPr)Au–OO–Au(IPr) (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene). The reaction kinetics are reported, as well as the reactivity of Au(I) hydrides with radical scavengers. American Chemical Society 2014-12-18 2015-06-08 /pmc/articles/PMC4482408/ /pubmed/26146435 http://dx.doi.org/10.1021/om501165z Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Roşca, Dragoş-Adrian Fernandez-Cestau, Julio Hughes, David L. Bochmann, Manfred Reactivity of Gold Hydrides: O(2) Insertion into the Au–H Bond |
title | Reactivity of Gold Hydrides: O(2) Insertion
into the Au–H Bond |
title_full | Reactivity of Gold Hydrides: O(2) Insertion
into the Au–H Bond |
title_fullStr | Reactivity of Gold Hydrides: O(2) Insertion
into the Au–H Bond |
title_full_unstemmed | Reactivity of Gold Hydrides: O(2) Insertion
into the Au–H Bond |
title_short | Reactivity of Gold Hydrides: O(2) Insertion
into the Au–H Bond |
title_sort | reactivity of gold hydrides: o(2) insertion
into the au–h bond |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482408/ https://www.ncbi.nlm.nih.gov/pubmed/26146435 http://dx.doi.org/10.1021/om501165z |
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