Selective coordination of coinage metals using orthogonal ligand scaffolds.

Group 11 metal complexes with their ability to form metallophilic interations are widely pursued to develop multifunctional luminescent materials. Heteronuclear coinage metal complexes are promising candidates to tune electronic and optical properties which are not readily accessed by their homometallic congeners. In this review, we present the concept of orthogonal ligands which are rationally designed to access heteronuclear coinage metal complexes and studied in terms of their photophysical properties. Bifunctional ligands containing soft and hard donor atoms have the potential of providing different coordination modes to selectively synthesise heterobimetallic complexes in a predictable manner. This review deals with ligand sets composed of pyridine, bipyridine- or iminopyridine-substituted NHCs featuring C–N coordination modes, phosphine-based N-heterocycles and amidinate ligand scaffolds comprising of P–N functionalities and mixed phosphine–phosphine oxide with P–O donor sites. Therefore, the scope of this perspective is the discussion of heteronuclear coinage metal complexes supported by recently developed bifunctional ligands in terms of their synthesis, coordination geometries and tunability of optical properties when compared to their homometallic analogues. [ABSTRACT FROM AUTHOR]