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Updated: Feb 8, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Rhodafuran from a methoxy(alkenyl)carbene by the rhoda-1,3,5-hexatriene route
M Talavera1, R Pereira-Cameselle, S Bolaño
1Departamento de Química Inorgánica, Universidad de Vigo, Campus Universitario, E-36310 Vigo, Spain. bgs@uvigo.es matalaveran@uvigo.es.
Abstract:
A methoxy(alkenyl)carbenerhodium complex [RhCp*Cl{[double bond, length as m-dash]C(OMe)CH[double bond, length as m-dash]CPh2}(PMe3)]PF6 (2) has been synthesized and used as the starting material for the study of the effect of the metal center (Rh vs. Ir) in the formation of new rhodacycle complexes. While η3 and η5 indenylrhodium complexes have been achieved by the C-H bond activation of a phenyl ring, insertion of terminal alkynes into the rhodium-carbene bond led to the first example of the synthesis of rhodafuran complexes through rhoda-1,3,5-hexatriene intermediates. This new method represents an efficient process to obtain metallafuran complexes.
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