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Decarbonylative ether dissection by iridium pincer complexes

A unique chain-rupturing transformation that converts an ether functionality into two hydrocarbyl units and carbon monoxide is reported, mediated by iridium(i) complexes supported by aminophenylphosphinite (NCOP) pincer ligands. The decarbonylation, which involves the cleavage of one C–C bond, one C...

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Autores principales: Yoo, Changho, Dodge, Henry M., Farquhar, Alexandra H., Gardner, Kristen E., Miller, Alexander J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162749/
https://www.ncbi.nlm.nih.gov/pubmed/34123222
http://dx.doi.org/10.1039/d0sc03736b
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author Yoo, Changho
Dodge, Henry M.
Farquhar, Alexandra H.
Gardner, Kristen E.
Miller, Alexander J. M.
author_facet Yoo, Changho
Dodge, Henry M.
Farquhar, Alexandra H.
Gardner, Kristen E.
Miller, Alexander J. M.
author_sort Yoo, Changho
collection PubMed
description A unique chain-rupturing transformation that converts an ether functionality into two hydrocarbyl units and carbon monoxide is reported, mediated by iridium(i) complexes supported by aminophenylphosphinite (NCOP) pincer ligands. The decarbonylation, which involves the cleavage of one C–C bond, one C–O bond, and two C–H bonds, along with formation of two new C–H bonds, was serendipitously discovered upon dehydrochlorination of an iridium(iii) complex containing an aza-18-crown-6 ether macrocycle. Intramolecular cleavage of macrocyclic and acyclic ethers was also found in analogous complexes featuring aza-15-crown-5 ether or bis(2-methoxyethyl)amino groups. Intermolecular decarbonylation of cyclic and linear ethers was observed when diethylaminophenylphosphinite iridium(i) dinitrogen or norbornene complexes were employed. Mechanistic studies reveal the nature of key intermediates along a pathway involving initial iridium(i)-mediated double C–H bond activation.
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spelling pubmed-81627492021-06-11 Decarbonylative ether dissection by iridium pincer complexes Yoo, Changho Dodge, Henry M. Farquhar, Alexandra H. Gardner, Kristen E. Miller, Alexander J. M. Chem Sci Chemistry A unique chain-rupturing transformation that converts an ether functionality into two hydrocarbyl units and carbon monoxide is reported, mediated by iridium(i) complexes supported by aminophenylphosphinite (NCOP) pincer ligands. The decarbonylation, which involves the cleavage of one C–C bond, one C–O bond, and two C–H bonds, along with formation of two new C–H bonds, was serendipitously discovered upon dehydrochlorination of an iridium(iii) complex containing an aza-18-crown-6 ether macrocycle. Intramolecular cleavage of macrocyclic and acyclic ethers was also found in analogous complexes featuring aza-15-crown-5 ether or bis(2-methoxyethyl)amino groups. Intermolecular decarbonylation of cyclic and linear ethers was observed when diethylaminophenylphosphinite iridium(i) dinitrogen or norbornene complexes were employed. Mechanistic studies reveal the nature of key intermediates along a pathway involving initial iridium(i)-mediated double C–H bond activation. The Royal Society of Chemistry 2020-09-24 /pmc/articles/PMC8162749/ /pubmed/34123222 http://dx.doi.org/10.1039/d0sc03736b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Yoo, Changho
Dodge, Henry M.
Farquhar, Alexandra H.
Gardner, Kristen E.
Miller, Alexander J. M.
Decarbonylative ether dissection by iridium pincer complexes
title Decarbonylative ether dissection by iridium pincer complexes
title_full Decarbonylative ether dissection by iridium pincer complexes
title_fullStr Decarbonylative ether dissection by iridium pincer complexes
title_full_unstemmed Decarbonylative ether dissection by iridium pincer complexes
title_short Decarbonylative ether dissection by iridium pincer complexes
title_sort decarbonylative ether dissection by iridium pincer complexes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162749/
https://www.ncbi.nlm.nih.gov/pubmed/34123222
http://dx.doi.org/10.1039/d0sc03736b
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