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Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity

We report an unusual series of discrete iodosyl- and iodoxyarene adducts of Co. The formation of these adducts was confirmed by a suite of techniques including single crystal X-ray diffraction. The reactivity of these adducts with O-atom acceptors and an H-atom donor has been investigated with parti...

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Autores principales: Hill, Ethan A., Kelty, Margaret L., Filatov, Alexander S., Anderson, John S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958341/
https://www.ncbi.nlm.nih.gov/pubmed/29896391
http://dx.doi.org/10.1039/c8sc01167b
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author Hill, Ethan A.
Kelty, Margaret L.
Filatov, Alexander S.
Anderson, John S.
author_facet Hill, Ethan A.
Kelty, Margaret L.
Filatov, Alexander S.
Anderson, John S.
author_sort Hill, Ethan A.
collection PubMed
description We report an unusual series of discrete iodosyl- and iodoxyarene adducts of Co. The formation of these adducts was confirmed by a suite of techniques including single crystal X-ray diffraction. The reactivity of these adducts with O-atom acceptors and an H-atom donor has been investigated with particular focus on elucidating mechanistic details. Detailed kinetic analysis allows for discrimination between proposed oxo and adduct mediated mechanisms. In particular, these reactions have been interrogated by competition experiments with isotopically labelled mixtures which shows that all of the studied adducts display a large KIE. These studies suggest different mechanisms may be relevant depending on subtle substituent changes in the adduct complexes. Reactivity data are consistent with the involvement of a transient oxo complex in one case, while the two other systems appear to react with substrates directly as iodosyl- or iodoxyarene adducts. These results support that reactivity typically ascribed to metal-oxo complexes, such as O-atom transfer and C–H activation, can also be mediated by discrete transition metal iodosyl- or iodoxyarene adducts that are frequent intermediates in the generation of oxo complexes. The influence of additional Lewis acids such as Sc(3+) on the reactivity of these systems has also been investigated.
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spelling pubmed-59583412018-06-12 Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity Hill, Ethan A. Kelty, Margaret L. Filatov, Alexander S. Anderson, John S. Chem Sci Chemistry We report an unusual series of discrete iodosyl- and iodoxyarene adducts of Co. The formation of these adducts was confirmed by a suite of techniques including single crystal X-ray diffraction. The reactivity of these adducts with O-atom acceptors and an H-atom donor has been investigated with particular focus on elucidating mechanistic details. Detailed kinetic analysis allows for discrimination between proposed oxo and adduct mediated mechanisms. In particular, these reactions have been interrogated by competition experiments with isotopically labelled mixtures which shows that all of the studied adducts display a large KIE. These studies suggest different mechanisms may be relevant depending on subtle substituent changes in the adduct complexes. Reactivity data are consistent with the involvement of a transient oxo complex in one case, while the two other systems appear to react with substrates directly as iodosyl- or iodoxyarene adducts. These results support that reactivity typically ascribed to metal-oxo complexes, such as O-atom transfer and C–H activation, can also be mediated by discrete transition metal iodosyl- or iodoxyarene adducts that are frequent intermediates in the generation of oxo complexes. The influence of additional Lewis acids such as Sc(3+) on the reactivity of these systems has also been investigated. Royal Society of Chemistry 2018-04-23 /pmc/articles/PMC5958341/ /pubmed/29896391 http://dx.doi.org/10.1039/c8sc01167b Text en This journal is © The Royal Society of Chemistry 2018 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Hill, Ethan A.
Kelty, Margaret L.
Filatov, Alexander S.
Anderson, John S.
Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity
title Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity
title_full Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity
title_fullStr Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity
title_full_unstemmed Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity
title_short Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity
title_sort isolable iodosylarene and iodoxyarene adducts of co and their o-atom transfer and c–h activation reactivity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958341/
https://www.ncbi.nlm.nih.gov/pubmed/29896391
http://dx.doi.org/10.1039/c8sc01167b
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