2010OrganometallicsRequires access

Synthesis and Structure of the Dimethyl Sulfide Adducts of Mono- and Bis(pentafluorophenyl)borane

A. T. Fuller, David L. Hughes, S.J. Lancaster, Callum M. White

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Abstract

The borane dimethyl sulfide adduct H 3 B·SMe 2 and the diethyl ether adduct of tris(pentafluorophenyl)borane, (C 6 F 5 ) 3 B·OEt 2, undergo facile exchange of hydride and pentafluorophenyl ligands, yielding (C 6 F 5 ) 2 HB·SMe 2 ( 1 ) and (C 6 F 5 )H 2 B·SMe 2 ( 2 ) depending upon the ratio of reagents used. In the presence of excess dimethyl sulfide, both compounds can be isolated as colorless crystals, which have been structurally characterized.

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What this paper is about

The borane dimethyl sulfide adduct H 3 B·SMe 2 and the diethyl ether adduct of tris(pentafluorophenyl)borane, (C 6 F 5 ) 3 B·OEt 2, undergo facile exchange of hydride and pentafluorophenyl ligands, yielding (C 6 F 5 ) 2 HB·SMe 2 ( 1 ) and (C 6 F 5 )H 2 B·SMe 2 ( 2 ) depending upon the ratio of reagents used. In the presence of excess dimethyl sulfide, both compounds can be isolated as colorless crystals, which have been structurally characterized.

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Available abstract

The borane dimethyl sulfide adduct H 3 B·SMe 2 and the diethyl ether adduct of tris(pentafluorophenyl)borane, (C 6 F 5 ) 3 B·OEt 2, undergo facile exchange of hydride and pentafluorophenyl ligands, yielding (C 6 F 5 ) 2 HB·SMe 2 ( 1 ) and (C 6 F 5 )H 2 B·SMe 2 ( 2 ) depending upon the ratio of reagents used. In the presence of excess dimethyl sulfide, both compounds can be isolated as colorless crystals, which have been structurally characterized.

Key concepts: Chemistry, Borane, Adduct, Dimethyl sulfide, Reagent, Hydride, Medicinal chemistry, Sulfide

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