A new type of oxidative addition of an iodoarene to a Pd(II) complex
Inmaculada Vicente-Hernández1, María-Teresa Chicote, José Vicente
1Grupo de Química Organometálica, Departamento de Química Inorgánica, Facultad de Química, Universidad de Murcia, Apartado 4021, Murcia, 30071, Spain. jvs1@um.es mch@um.es.
Abstract:
Oxidative addition of N-(2-iodophenyl)formamide to Pd(dba)2 (dba = dibenzylideneacetone) in the presence of 4,4'-ditertbutyl-2,2'-bipyridine ((t)Bubpy) produces [Pd(C6H4NHCHO-2)I((t)Bubpy)] (1) which inserts 2-iodophenyl isocyanide to give [Pd{C(=NC6H4I-2)C6H4NHCHO-2}I((t)Bubpy)] (2). Dehydroiodination of 2 with Tl(acac) (acacH = acetylacetone) gives the stable Pd(IV) complex OC-6-35-[Pd{C,N,N-C(=NC6H4-2)C6H4NCHO-2}I((t)Bubpy)] (4) likely resulting from the spontaneous oxidative addition of the I-Ar moiety present in the unstable intermediate Pd(II) complex [Pd{C,N-C(=NC6H4I-2)C6H4NCHO-2}((t)Bubpy)] (3). The crystal structure of 4 shows various C-H···O hydrogen bonds resulting in chains of dimers stacked along the a axis.
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