A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand

Anita Leitgeb; Mudassar E. Abbas; Roland C. Fischer; Albert Poater; Luigi Cavallo; Christian Slugovc

doi:10.1039/c2cy20311a

A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand

Anita Leitgeb, Mudassar E. Abbas, Roland C. Fischer, Albert Poater, Luigi Cavallo, Christian Slugovc

Research output: Contribution to journal › Article › peer-review

49 Scopus citations

Abstract

An olefin metathesis catalyst featuring a SIPr NHC and an ester chelating carbene ligand is introduced. In contrast to its previously published SIMes analogue, only the trans dichloro configurated isomer was obtained. The two counterparts are tested in various olefin metathesis reactions, revealing a striking superiority of the new complex in the cross metathesis of olefins with methyl vinyl ketone allowing for full conversion with only 500 ppm catalyst loading. © 2012 The Royal Society of Chemistry.

Original language	English (US)
Pages (from-to)	1640
Journal	Catalysis Science & Technology
Volume	2
Issue number	8
DOIs	https://doi.org/10.1039/c2cy20311a
State	Published - 2012

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: Financial support of this work from the Higher Education Commission of Pakistan (for M. A.) and the European Community (CP-FP 211468-2 EUMET) is gratefully acknowledged. A. P. thanks the Spanish MINECO for a Ramon y Cajal contract (ref. RYC-2009-05226) and the European Commission for a Career Integration Grant (CIG09-GA-2011-293900). The provision of complex M32 by Prof. S. P. Nolan and team (Univ. St. Andrews) is highly appreciated.

ASJC Scopus subject areas

Catalysis

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10.1039/c2cy20311a

Cite this

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title = "A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand",

abstract = "An olefin metathesis catalyst featuring a SIPr NHC and an ester chelating carbene ligand is introduced. In contrast to its previously published SIMes analogue, only the trans dichloro configurated isomer was obtained. The two counterparts are tested in various olefin metathesis reactions, revealing a striking superiority of the new complex in the cross metathesis of olefins with methyl vinyl ketone allowing for full conversion with only 500 ppm catalyst loading. {\textcopyright} 2012 The Royal Society of Chemistry.",

author = "Anita Leitgeb and Abbas, {Mudassar E.} and Fischer, {Roland C.} and Albert Poater and Luigi Cavallo and Christian Slugovc",

note = "KAUST Repository Item: Exported on 2020-10-01 Acknowledgements: Financial support of this work from the Higher Education Commission of Pakistan (for M. A.) and the European Community (CP-FP 211468-2 EUMET) is gratefully acknowledged. A. P. thanks the Spanish MINECO for a Ramon y Cajal contract (ref. RYC-2009-05226) and the European Commission for a Career Integration Grant (CIG09-GA-2011-293900). The provision of complex M32 by Prof. S. P. Nolan and team (Univ. St. Andrews) is highly appreciated.",

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AU - Leitgeb, Anita

AU - Abbas, Mudassar E.

AU - Fischer, Roland C.

AU - Poater, Albert

AU - Cavallo, Luigi

AU - Slugovc, Christian

N1 - KAUST Repository Item: Exported on 2020-10-01 Acknowledgements: Financial support of this work from the Higher Education Commission of Pakistan (for M. A.) and the European Community (CP-FP 211468-2 EUMET) is gratefully acknowledged. A. P. thanks the Spanish MINECO for a Ramon y Cajal contract (ref. RYC-2009-05226) and the European Commission for a Career Integration Grant (CIG09-GA-2011-293900). The provision of complex M32 by Prof. S. P. Nolan and team (Univ. St. Andrews) is highly appreciated.

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N2 - An olefin metathesis catalyst featuring a SIPr NHC and an ester chelating carbene ligand is introduced. In contrast to its previously published SIMes analogue, only the trans dichloro configurated isomer was obtained. The two counterparts are tested in various olefin metathesis reactions, revealing a striking superiority of the new complex in the cross metathesis of olefins with methyl vinyl ketone allowing for full conversion with only 500 ppm catalyst loading. © 2012 The Royal Society of Chemistry.

AB - An olefin metathesis catalyst featuring a SIPr NHC and an ester chelating carbene ligand is introduced. In contrast to its previously published SIMes analogue, only the trans dichloro configurated isomer was obtained. The two counterparts are tested in various olefin metathesis reactions, revealing a striking superiority of the new complex in the cross metathesis of olefins with methyl vinyl ketone allowing for full conversion with only 500 ppm catalyst loading. © 2012 The Royal Society of Chemistry.

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JF - Catalysis Science & Technology

IS - 8

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A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand

Abstract

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CCDC 866162: Experimental Crystal Structure Determination : dichloro-(1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene)-(2-(isopropoxycarbonyl)-5-methoxybenzylidene)-ruthenium dichloromethane solvate

Cite this

A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand

Abstract

Bibliographical note

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Datasets

CCDC 866162: Experimental Crystal Structure Determination : dichloro-(1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene)-(2-(isopropoxycarbonyl)-5-methoxybenzylidene)-ruthenium dichloromethane solvate

Cite this