Document Type

Article

Language

eng

Format of Original

8 p.

Publication Date

12-1-2009

Publisher

Elsevier

Source Publication

Inorganic Chimica Acta

Source ISSN

0020-1693

Abstract

Addition of phenyldi(2-thienyl)phosphine (PPhTh2) to [Re2(CO)10−n(NCMe)n] (n = 1, 2) affords the substitution products [Re2(CO)10−n(PhPTh2)n] (1, 2) together with small amounts of fac-[ClRe(CO)3(PPhTh2)2] (3) (n = 2). Reaction of [Re2(CO)10] with PPhTh2in refluxing xylene affords a mixture which includes 2, [Re2(CO)7(PPhTh2)(μ-PPhTh)(μ-H)] (4), [Re2(CO)7(PPhTh2)(μ-PPhTh)(μ-η11(S)-C4H3S)] (5) and mer-[HRe(CO)3(PPhTh2)2] (6). Phosphido-bridged 4 and 5 are formed by the carbon–phosphorus bond cleavage of the coordinated PPhTh2 ligand, the cleaved thienyl group being retained in the latter. Reaction of [Mn2(CO)10] with PPhTh2 in refluxing toluene affords [Mn2(CO)9(PPhTh2)] (7) and the carbon–phosphorus bond cleavage products [Mn2(CO)6(μ-PPhTh)(μ-η15-C4H3S)] (8) and [Mn2(CO)5(PPhTh2)(μ-PPhTh)(μ-η15-C4H3S)] (9). Both 8 and 9 contain a bridging thienyl ligand which is bonded to one manganese atom in a η5-fashion.

Comments

Accepted version. Inorganica Chimica Acta, Vol. 362, No. 15 (December 1, 2009): 5175-5182. DOI. © 2009 Elsevier. Used with permission.

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