Reactivity of molybdenum and rhenium hydroxo complexes toward organic electrophiles: reactions that afford carboxylato products

Cuesta, L and Hevia, E and Morales, D and Perez, J and Riera, L and Miguel, D (2006) Reactivity of molybdenum and rhenium hydroxo complexes toward organic electrophiles: reactions that afford carboxylato products. Organometallics, 25 (7). pp. 1717-1722. ISSN 0276-7333 (https://doi.org/10.1021/om051081g)

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Abstract

The reactions of the hydroxo complexes [Mo(OH)(eta(3)-methallyl)(CO)(2)(phen)] (1) and [Re(OH)(CO)(3)(Me-2-biPY)] (2) (phen = 1,10-phenanthroline, Me-2-bipy= 4,4'-dimethyl-2,2'-bipyridine) with maleic anhydride, phenyl(ethyl)ketene, diphenylketene, and rac-lactide afford new carboxylato complexes. The molybdenum and rhenium hydroxo complexes react in the same way, and their reactions are quantitative. The products, some of which have been characterized by X-ray diffraction, feature monodentate O-bonded carboxylato ligands, and their treatment with triflic acid yields the triflato complexes [Mo(OTf)(eta(3)-methallyl)(CO)(2)(phen)] and [Re(OTf)(CO)(3)(Me-2-bipy)] and the corresponding free carboxylic acid.

ORCID iDs

Cuesta, L, Hevia, E ORCID logoORCID: https://orcid.org/0000-0002-3998-7506, Morales, D, Perez, J, Riera, L and Miguel, D;
CORE (COnnecting REpositories)