Nickel(II) Analogues of Phosphorescent Platinum(II) Complexes with Picosecond Excited‐State Decay

Abstract

Square‐planar Ni(II) complexes are interesting as cheaper and more sustainable alternatives to Pt(II) luminophores widely used in lighting and photocatalysis. We investigated the excited‐state behavior of two Ni(II) complexes, which are isostructural with two luminescent Pt(II) complexes. The initially excited singlet metal‐to‐ligand charge transfer (1MLCT) excited states in the Ni(II) complexes decay to metal‐centered (3MC) excited states within less than 1 picosecond, followed by non‐radiative relaxation of the 3MC states to the electronic ground state within 9 ‐ 21 ps. This contrasts with the population of an emissive triplet ligand‐centered (3LC) excited state upon excitation of the Pt(II) analogues. Structural distortions of the Ni(II) complexes are responsible for this discrepant behavior and lead to dark 3MC states far lower in energy than the luminescent 3LC states of Pt(II) compounds. Our findings suggest that if these structural distortions could be restricted by more rigid coordination environments and stronger ligand fields, the excited‐state relaxation in four‐coordinate Ni(II) complexes could be decelerated such that luminescent 3LC or 3MLCT excited states become accessible. These insights are relevant to make Ni(II) fit for photophysical and photochemical applications that relied on Pt(II) until now.