Synthesis of New Donor-Substituted Biphenyls: Pre-ligands for Highly Luminescent Gold(III) Pincer Complexes

We herein report on new synthetic strategies for the preparation of pyridine and imidazole substituted 2,2'-dihalo biphenyls. These structures are pre-ligands suitable for the preparation of respective stannoles. The latter can successfully be transmetalated to K[AuCl4] forming non-palindromic [(C boolean AND C boolean AND D)Au-III] pincer complexes featuring a lateral pyridine (D=N) or N-heterocyclic carbene (NHC, D=C') donor. The latter is the first report on a pincer complex with two formally anionic sp(2) and one carbenic carbon donor. The [(C boolean AND C boolean AND D)Au-III] complexes show intense phosphorescence in solution at room temperature. We discuss the developed multistep strategy and touch upon synthetic challenges. The prepared complexes have been fully characterized including X-ray diffraction analysis. The gold(III) complexes' photophysical properties have been investigated by absorption and emission spectroscopy as well as quantum chemical calculations on the quasi-relativistic two-component TD-DFT and GW/Bethe-Salpeter level including spin-orbit coupling. Thus, we shed light on the electronic influence of the non-palindromic pincer ligand and reveal non-radiative relaxation pathways of the different ligands employed.