Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis

<p>The synthesis of rhodium complexes with weakly binding highly fluorinated benzene ligands is described: 1,2,3‐F<sub>3</sub>C<sub>6</sub>H<sub>3</sub>, 1,2,3,4‐F<sub>4</sub>C<sub>6</sub>H<sub>2</sub>&nbsp;and 1,2,3,4...

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Main Authors: McKay, A, Barwick–Silk, J, Savage, M, Willis, M, Weller, A
Format: Journal article
Language:English
Published: Wiley 2019
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author McKay, A
Barwick–Silk, J
Savage, M
Willis, M
Weller, A
author_facet McKay, A
Barwick–Silk, J
Savage, M
Willis, M
Weller, A
author_sort McKay, A
collection OXFORD
description <p>The synthesis of rhodium complexes with weakly binding highly fluorinated benzene ligands is described: 1,2,3‐F<sub>3</sub>C<sub>6</sub>H<sub>3</sub>, 1,2,3,4‐F<sub>4</sub>C<sub>6</sub>H<sub>2</sub>&nbsp;and 1,2,3,4,5‐F<sub>5</sub>C<sub>6</sub>H are shown to bind with cationic [Rh(Cy<sub>2</sub>P(CH<sub>2</sub>)<sub><em>x</em></sub>PCy<sub>2</sub>)]<sup>+</sup>&nbsp;fragments (<em>x=</em>1, 2). Their structures and reactivity with alkenes, and use in catalysis for promoting the Tishchenko reaction of a simple aldehyde, are demonstrated. Key to the synthesis of these complexes is the highly concentrated reaction conditions and use of the [Al{OC(CF<sub>3</sub>)<sub>3</sub>}<sub>4</sub>]<sup>&minus;</sup>&nbsp;anion.</p>
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spelling oxford-uuid:e7b1f205-39dc-4034-80fc-e05f9540e4912022-03-27T10:40:51ZSynthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysisJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e7b1f205-39dc-4034-80fc-e05f9540e491EnglishSymplectic Elements at OxfordWiley2019McKay, ABarwick–Silk, JSavage, MWillis, MWeller, A<p>The synthesis of rhodium complexes with weakly binding highly fluorinated benzene ligands is described: 1,2,3‐F<sub>3</sub>C<sub>6</sub>H<sub>3</sub>, 1,2,3,4‐F<sub>4</sub>C<sub>6</sub>H<sub>2</sub>&nbsp;and 1,2,3,4,5‐F<sub>5</sub>C<sub>6</sub>H are shown to bind with cationic [Rh(Cy<sub>2</sub>P(CH<sub>2</sub>)<sub><em>x</em></sub>PCy<sub>2</sub>)]<sup>+</sup>&nbsp;fragments (<em>x=</em>1, 2). Their structures and reactivity with alkenes, and use in catalysis for promoting the Tishchenko reaction of a simple aldehyde, are demonstrated. Key to the synthesis of these complexes is the highly concentrated reaction conditions and use of the [Al{OC(CF<sub>3</sub>)<sub>3</sub>}<sub>4</sub>]<sup>&minus;</sup>&nbsp;anion.</p>
spellingShingle McKay, A
Barwick–Silk, J
Savage, M
Willis, M
Weller, A
Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis
title Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis
title_full Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis
title_fullStr Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis
title_full_unstemmed Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis
title_short Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine)]+ cations, and their use in synthesis and catalysis
title_sort synthesis of highly fluorinated arene complexes of rh chelating phosphine cations and their use in synthesis and catalysis
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