Copper(I) complexes of N-(aryl)pyridine-2-aldimines: Spectral, electrochemical and catalytic properties

The reactions of N-(aryl)pyridine-2-aldimines (L–R; R = OCH3, CH3, H, Cl and NO2), derived from pyridine-2-aldehyde and para-substituted anilines, with CuI in methanol under ambient conditions afford a series of brown complexes of the type [{Cu(L–R)I}2]. The structure of the [{Cu(L–OCH3)I}2] complex has been determined by X-ray crystallography. In these dimeric complexes the two copper centers are linked through an iodo-bridge, and the L–R ligands are coordinated to the metal center through the pyridine-nitrogen and imine-nitrogen. All the complexes show characteristic 1H NMR signals and intense MLCT transitions in the visible region. These complexes also show an emission near 465 nm, whilst they are excited at 340 nm, with relatively poor quantum yields (φ ∼0.002 at 298 K). Cyclic voltammetry on all the complexes shows two successive Cu(I)–Cu(II) oxidations on the positive side of SCE, and a reduction of the coordinated imine ligand on the negative side. These copper(I) complexes are found to efficiently catalyze Suzuki type C–C coupling reactions.

The reaction of N-(aryl)pyridine-2-aldimines (L–R; R = OCH3, CH3, H, Cl and NO2), derived from pyridine-2-aldehyde and para-substituted anilines, with CuI in methanol under ambient condition affords a series of dinuclear copper(I) complexes of the type [{Cu(L–R)I}2].Figure optionsDownload as PowerPoint slideHighlights
► Dinuclear copper(I) complexes of N-(aryl)pyridine-2-aldimines have been prepared.
► These complexes show emission in the visible region.
► They also efficiently catalyze Suzuki coupling reactions.