Activation of aromatic C−C bonds of 2,2’-bipyridine ligands

Abstract

4,4’-Disubstituted-2,2′-bipyridine ligands coordinated to Mo and Re cationic fragments become dearomatized by an intramolecular nucleophilic attack from a deprotonated N-alkylimidazole ligand in cis disposition. The subsequent protonation of these neutral complexes takes place on a pyridine carbon atom rather than at nitrogen, weakening an aromatic C−C bond and affording a dihydropyridyl moiety. Computational calculations allowed for the rationalization of the formation of the experimentally obtained products over other plausible alternatives.Financialsupport from Ministerio de Economía y Competitividad/FEDER (grant CTQ2015-70231-P) and Principado de Asturias (grant GRUPIN14-103) is gratefully acknowledged. J.D.thanks COMPUTAEX for granting access to LUSITANIA supercomputing facilities.Peer Reviewe