Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/36804
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Título : Experimental and Computational Studies on the Iridium Activation of Aliphatic and Aromatic C-H Bonds of Alkyl Aryl Ethers and Related Molecules
Autor : Lara, Patricia, Paneque, Margarita, López Poveda, Manuel, López Santos, Laura, Villar Valpuesta, José E., Carmona Guzmán, Ernesto, Moncho, Salvador, Ujaque, Gregori, Lledós, Agustí, Álvarez, Eleuterio, Mereiter, Kurt
Palabras clave : Carbenes
C-H activation
Density functional calculations
Hydride complexes
Iridium
Fecha de publicación : 5-Aug-2009
Editor: Wiley-VCH
Resumen: Reaction of the IrIII complex [(TpMe2)Ir(C6H5)2(N2)] (1⋅N2) with ortho-cresol (2-methylphenol) occurs with cleavage of the O-H and two C(sp3)-H bonds of the phenol and formation of the electrophilic hydride alkylidene derivative [(TpMe2)Ir(H){=C(H)C6H4-o-O}] (2). The analogous reaction of 2-ethylphenol gives a related product 3. Both 2 and 3 have been shown to be identical to the minor, unidentified products of the already reported reactions of 1 with anisole and phenetole, respectively. Thus, in addition to the route that leads to the known heteroatom-stabilized hydride carbene [(TpMe2)Ir(H){=C(H)OC6H4- o-}] (B), anisole can react with 1 with cleavage of the O=CH3 bond and formation of a new carbon–carbon bond. In contrast, only C-H bond-activation products with structures akin to B result from 1⋅N2 and 3,5-dimethylanisole (complex 8) or 4-fluoroanisole (9). Using anisole as a model, a computational study of the triple C-H bond activation (two aliphatic C-H bonds plus an ortho-metalation reaction) that is responsible for the formation of these heteroatom-stabilized hydride carbenes has been undertaken.
Descripción : 12 páginas, 7 figuras, 1 tabla, 6 esquemas
Versión del editor: http://dx.doi.org/10.1002/chem.200900646
URI : http://hdl.handle.net/10261/36804
ISSN: 0947-6539
DOI: 10.1002/chem.200900646
Citación : Chemistry - a European Journal 15(36): 9034-9045 (2009)
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