Tuning Pt(II)‐Based Donor‐Acceptor Systems Through Ligand Design: Effects on Frontier Orbitals, Redox Potentials, Vis‐NIR Absorptions, Electrochromism and Photocatalysis

Asymmetric platinum donor-acceptor complexes [(pimp)Pt(Q(2-) )] are presented in this work, in which pimp=[(2,4,6-trimethylphenylimino)methyl]pyridine and Q(2-) =catecholate-type donor ligands. The properties of the complexes are evaluated as a function of the donor ligands, and correlations are drawn among electrochemical, optical, and theoretical data. Special focus has been put on the spectroelectrochemical investigation of the complexes featuring sulfonyl-substituted phenylendiamide ligands, which show redox-induced linkage isomerism upon oxidation. Time-dependent density functional theory (TD-DFT) as well as electron flux density analysis have been employed to rationalize the optical spectra of the complexes and their reactivity. Compound 1 ([(pimp)Pt(Q(2-) )] with Q(2-) =3,5-di-tert-butylcatecholate) was shown to be an efficient photosensitizer for molecular oxygen and was subsequently employed in photochemical cross-dehydrogenative coupling (CDC) reactions. The results thus display new avenues for donor-acceptor systems, including their role as photocatalysts for organic transformations, and the possibility to introduce redox-induced linkage isomerism in these compounds through the use of sulfonamide substituents on the donor ligands.