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Issue 22, 2006
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Use of the tetrahydroborate ligand as “gate-keeper” and protected hydride ligand: preparation and study of alkyl hydride and acyl hydride complexes of ruthenium(II)

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Abstract

Complex 3, [Ru(η2-BH4)(CO)(Et)L2] (L = PMe2Ph) can be converted by nucleophiles L′ {a, PMe2Ph; b, P(OMe)3; c, Me3CNC; d, CO} to alkyl and acyl complexes [Ru(η1-BH4)(CO)(Et)L2L′] (4a), [Ru(η2-BH4)(COEt)L2L′] (5a–d), and [Ru(η1-BH4)(COEt)L2L′2] (7d and isomers 7c and 10c). Deprotection can then be achieved under conditions mild enough to allow study of the resulting alkyl hydride complexes [Ru(CO)(Et)HL2L′] (1a, 1b) and acyl hydride complexes [Ru(COEt)HL2L′2] (8c, 8d) prior to elimination of ethane and propanal respectively, with formation of ruthenium(0) complexes [Ru(CO)L2L′2] (6a, 6b, 6d). With Me3CNC, however, the final product is (depending on the solvent used) [Ru(CNCMe3)2{C(H)NCMe3}(COEt)L2] (9c) or [Ru(CNCMe3)3(COEt)L2]+ (11c). Successive treatment of [Ru(η2-BH4)(CO)HL2], 2, with ethene and then CO yields propanal, but turning this into a catalytic cycle is hindered by the greater readiness of 5d to yield propanal non-catalytically (reacting with CO) than catalytically (reacting with H2).

Graphical abstract: Use of the tetrahydroborate ligand as “gate-keeper” and protected hydride ligand: preparation and study of alkyl hydride and acyl hydride complexes of ruthenium(ii)

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Publication details

The article was received on 04 Jan 2006, accepted on 13 Feb 2006 and first published on 06 Mar 2006


Article type: Paper
DOI: 10.1039/B600036C
Citation: Dalton Trans., 2006,0, 2661-2670
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    Use of the tetrahydroborate ligand as “gate-keeper” and protected hydride ligand: preparation and study of alkyl hydride and acyl hydride complexes of ruthenium(II)

    S. B. Duckett, J. P. Lowe and R. J. Mawby, Dalton Trans., 2006, 0, 2661
    DOI: 10.1039/B600036C

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