Abstract
Reaction of [Ru3(CO)9(μ3-CO)(μ3-NOMe)] 1 with stoichiometric amounts of the hydrido complex [(η5-C5H5)Mo(CO)3H] in THF at room temperature (r.t.) for 3 days affords the isolation of two new heterometallic trinuclear clusters namely [Ru2Mo(μ-H)(CO)8(η5-C5H5)(μ3-NOMe)] 2 and [Ru2Mo(μ-H)(CO)8(η5-C5H5)(μ3-NH)] 3 which both consist of a triangular Ru2Mo core capped by a NR fragment (2: R=OMe; 3: R=H). However, the reaction of 1 with the organomercurial derivative [{(η5-C5H5)Mo(CO)3}2Hg] resulted in the formation of a pentanuclear complex [Ru3(CO)10(μ-NH2)(μ3-Hg){Mo(η5-C5H5)(CO)3}] 4 in which a (η5-C5H5)Mo(CO)3Hg fragment bridges the Ru3core on the opposite side of the amido group.
Original language | English |
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Pages (from-to) | 323-329 |
Number of pages | 7 |
Journal | Journal of Organometallic Chemistry |
Volume | 577 |
Issue number | 2 |
DOIs | |
Publication status | Published - 1 Apr 1999 |
Externally published | Yes |
Keywords
- Cluster
- Methoxynitrido
- Molybdenum
- Nitrene
- Ruthenium
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry