The Rational Synthesis of Tetranuclear Heterometallic Butterfly Clusters: Reactions of [M2(CO)6(μ-pyS)2] (M = Re, Mn) with Group VIII Metal Carbonyls

Document Type

Article

Language

eng

Format of Original

10 p.

Publication Date

2010

Publisher

Royal Society of Chemistry

Source Publication

New Journal of Chemistry

Source ISSN

1144-0546

Abstract

Heating [Os3(CO)10(NCMe)2] with [M2(CO)6(μ-pyS)2] (M = Re, Mn) (1–2) in benzene affords tetranuclear mixed-metal butterfly clusters [MOs3(CO)13(μ3-pyS)] (3–4). Similar reactions with Ru3(CO)12 give [MRu3(CO)133-pyS)] (5–6); however, when the latter is carried out in toluene the tetraruthenium sulfido cluster [Ru4(CO)12(μ-py)24-S)] (7) is the major product. Treatment of Fe3(CO)12 with 1 in refluxing toluene affords the mixed-metal sulfido cluster, [Fe2Re2(CO)13(μ-py)(μ-pyS)(μ4-S)] (8), while a similar reaction with 2 furnishes the tetrairon cluster [Fe4(CO)12(μ-py)24-S)] (9). Addition of PPh3 to 3 in the presence of Me3NO affords both the mono- and bis(phosphine)-substituted products [ReOs3(CO)12(PPh3)(μ3-pyS)] (10) and [ReOs3(CO)11(PPh3)23-pyS)] (11), respectively. All new complexes have been characterized by a combination of spectroscopic data and single-crystal X-ray diffraction studies.

Comments

New Journal of Chemistry, Vol. 34, No. 9 (2010): 1875-1884. DOI.

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