Issue 23, 2000

Use of the monocationic fragment [Ru(η5-C5H5)(MeCN)3]+ as an ionic coupling reagent in the synthesis of mixed-metal phosphine clusters

Abstract

Deprotonation of [Os3H2(CO)10(PPh3)], with DBU (1,8-diazabicyclo[5.4.0]undec-7-ene), and subsequent treatment with the ionic coupling reagent [Ru(η5-C5H5)(MeCN)3][PF6] afforded the tetrahedral cluster [Os3H(CO)10(PPh3){Ru(η5-C5H5)}]. Reduction of the trinuclear osmium cluster [Os3(CO)11(PPh3)] with K/Ph2CO and subsequent coupling with [Ru(η5-C5H5)(MeCN)3][PF6] yielded the pentanuclear clusters [Os3(CO)11(PPh3){Ru(η5-C5H5)}2], [Os3H2(CO)11(PPh3){Ru(η5-C5H5)}2] and the butterfly cluster [Os3H(CO)11(PPh3){Ru(η5-C5H5)}]. In an analogous reaction using [Os3(CO)11{P(OMe)3}] only one complex [Os3(CO)11{P(OMe)3}{Ru(η5-C5H5)}2] was isolated. This undergoes an orthometallation when heated under reflux in toluene to yield the novel spiked tetrahedral cluster [Os3Ru2H(CO)11{P(OMe)3}(η5-C5H5)(μ35-C5H4)]. All the new complexes have been characterised spectroscopically and the molecular and crystal structures of three have been determined by single-crystal X-ray diffraction. The structure of [Os3Ru2H(CO)11{P(OMe)3}(η5-C5H5)(μ35-C5H4)] shows an uncommon μ35-bonding mode for the deprotonated cyclopentadiene ring.

Supplementary files

Article information

Article type
Paper
Submitted
17 Aug 2000
Accepted
09 Oct 2000
First published
15 Nov 2000

J. Chem. Soc., Dalton Trans., 2000, 4297-4303

Use of the monocationic fragment [Ru(η5-C5H5)(MeCN)3]+ as an ionic coupling reagent in the synthesis of mixed-metal phosphine clusters

R. Buntem, J. F. Gallagher, J. Lewis, P. R. Raithby<img border="0" src="https://www.rsc.org/images/entities/char_200a.gif" alt=" " xmlns="http://www.rsc.org/schema/rscart38" />, M. Rennie and G. P. Shields, J. Chem. Soc., Dalton Trans., 2000, 4297 DOI: 10.1039/B006746F

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