Backbone tuning in indenylidene–ruthenium complexes bearing an unsaturated N-heterocyclic carbene
The steric and electronic influence of backbone substitution in IMes-based (IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene) N-heterocyclic carbenes (NHC) was probed by synthesizing the [RhCl(CO)2(NHC)] series of complexes to quantify experimentally the Tolman electronic parameter (electroni...
Ausführliche Beschreibung
Autor*in: |
César A. Urbina-Blanco [verfasserIn] Xavier Bantreil [verfasserIn] Hervé Clavier [verfasserIn] Alexandra M. Z. Slawin [verfasserIn] Steven P. Nolan [verfasserIn] |
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Englisch |
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2010 |
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Übergeordnetes Werk: |
In: Beilstein Journal of Organic Chemistry - Beilstein-Institut, 2005, 6(2010), 1, Seite 1120-1126 |
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Übergeordnetes Werk: |
volume:6 ; year:2010 ; number:1 ; pages:1120-1126 |
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DOI / URN: |
10.3762/bjoc.6.128 |
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DOAJ066383714 |
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César A. Urbina-Blanco misc QD241-441 misc N-heterocyclic carbene misc olefin metathesis misc percent buried volume misc ruthenium–indenylidene misc Tolman electronic parameter misc Science misc Q misc Organic chemistry Backbone tuning in indenylidene–ruthenium complexes bearing an unsaturated N-heterocyclic carbene |
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QD241-441 Backbone tuning in indenylidene–ruthenium complexes bearing an unsaturated N-heterocyclic carbene N-heterocyclic carbene olefin metathesis percent buried volume ruthenium–indenylidene Tolman electronic parameter |
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Backbone tuning in indenylidene–ruthenium complexes bearing an unsaturated N-heterocyclic carbene |
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The steric and electronic influence of backbone substitution in IMes-based (IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene) N-heterocyclic carbenes (NHC) was probed by synthesizing the [RhCl(CO)2(NHC)] series of complexes to quantify experimentally the Tolman electronic parameter (electronic) and the percent buried volume (%Vbur, steric) parameters. The corresponding ruthenium–indenylidene complexes were also synthesized and tested in benchmark metathesis transformations to establish possible correlations between reactivity and NHC electronic and steric parameters. |
abstractGer |
The steric and electronic influence of backbone substitution in IMes-based (IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene) N-heterocyclic carbenes (NHC) was probed by synthesizing the [RhCl(CO)2(NHC)] series of complexes to quantify experimentally the Tolman electronic parameter (electronic) and the percent buried volume (%Vbur, steric) parameters. The corresponding ruthenium–indenylidene complexes were also synthesized and tested in benchmark metathesis transformations to establish possible correlations between reactivity and NHC electronic and steric parameters. |
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The steric and electronic influence of backbone substitution in IMes-based (IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene) N-heterocyclic carbenes (NHC) was probed by synthesizing the [RhCl(CO)2(NHC)] series of complexes to quantify experimentally the Tolman electronic parameter (electronic) and the percent buried volume (%Vbur, steric) parameters. The corresponding ruthenium–indenylidene complexes were also synthesized and tested in benchmark metathesis transformations to establish possible correlations between reactivity and NHC electronic and steric parameters. |
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Backbone tuning in indenylidene–ruthenium complexes bearing an unsaturated N-heterocyclic carbene |
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