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Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i)

Catalytic activity of copper(i) complexes supported by phenanthroline-containing catenane ligands towards a new C(sp(3))–O dehydrogenative cross-coupling of phenols and bromodicarbonyls is reported. As the phenanthrolines are interlocked by the strong and flexible mechanical bond in the catenane, th...

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Autores principales: Zhu, Lihui, Li, Jiasheng, Yang, Jun, Au-Yeung, Ho Yu
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/PMC8163234/
https://www.ncbi.nlm.nih.gov/pubmed/34094485
http://dx.doi.org/10.1039/d0sc05133k
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author Zhu, Lihui
Li, Jiasheng
Yang, Jun
Au-Yeung, Ho Yu
author_facet Zhu, Lihui
Li, Jiasheng
Yang, Jun
Au-Yeung, Ho Yu
author_sort Zhu, Lihui
collection PubMed
description Catalytic activity of copper(i) complexes supported by phenanthroline-containing catenane ligands towards a new C(sp(3))–O dehydrogenative cross-coupling of phenols and bromodicarbonyls is reported. As the phenanthrolines are interlocked by the strong and flexible mechanical bond in the catenane, the active catalyst with an open copper coordination site can be revealed only transiently and the stable, coordinatively saturated Cu(i) pre-catalyst is quickly regenerated after substrate transformation. Compared with a control Cu(i) complex supported by non-interlocked phenanthrolines, the catenane-supported Cu(i) is highly efficient with a broad substrate scope, and can be applied in gram-scale transformations without a significant loss of the catalytic activity. This work demonstrates the advantages of the catenane ligands that provide a dynamic and responsive copper coordination sphere, highlighting the potential of the mechanical bond as a design element in transition metal catalyst development.
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spelling pubmed-81632342021-06-04 Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i) Zhu, Lihui Li, Jiasheng Yang, Jun Au-Yeung, Ho Yu Chem Sci Chemistry Catalytic activity of copper(i) complexes supported by phenanthroline-containing catenane ligands towards a new C(sp(3))–O dehydrogenative cross-coupling of phenols and bromodicarbonyls is reported. As the phenanthrolines are interlocked by the strong and flexible mechanical bond in the catenane, the active catalyst with an open copper coordination site can be revealed only transiently and the stable, coordinatively saturated Cu(i) pre-catalyst is quickly regenerated after substrate transformation. Compared with a control Cu(i) complex supported by non-interlocked phenanthrolines, the catenane-supported Cu(i) is highly efficient with a broad substrate scope, and can be applied in gram-scale transformations without a significant loss of the catalytic activity. This work demonstrates the advantages of the catenane ligands that provide a dynamic and responsive copper coordination sphere, highlighting the potential of the mechanical bond as a design element in transition metal catalyst development. The Royal Society of Chemistry 2020-11-01 /pmc/articles/PMC8163234/ /pubmed/34094485 http://dx.doi.org/10.1039/d0sc05133k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhu, Lihui
Li, Jiasheng
Yang, Jun
Au-Yeung, Ho Yu
Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i)
title Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i)
title_full Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i)
title_fullStr Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i)
title_full_unstemmed Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i)
title_short Cross dehydrogenative C–O coupling catalysed by a catenane-coordinated copper(i)
title_sort cross dehydrogenative c–o coupling catalysed by a catenane-coordinated copper(i)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163234/
https://www.ncbi.nlm.nih.gov/pubmed/34094485
http://dx.doi.org/10.1039/d0sc05133k
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