Abstract

Two novel bidentate C^C*spiro cyclometalated platinum(II) complexes comprising a spiro-conjugated bifluorene ligand and different β-diketonate auxiliary ligands are synthesized and characterized. Their preparation employs a robust and elaborate synthetic protocol commencing with an N-heterocyclic carbene precursor. Structural characterization by means of NMR techniques and solid-state structures validate the proposed and herein presented molecular scaffolds. Photophysical studies, including laser flash photolysis methods, reveal an almost exclusively ligand-centered triplet state, governed by the C^C*spiro-NHC ligand. The high triplet energies and the long triplet lifetimes in the order of 30 μs in solution make the complexes good candidates for light-emitting diode-driven photocatalysis, as initial energy transfer experiments reveal. In-depth time-dependent density functional theory investigations are in excellent accordance with our spectroscopic findings. The title compounds are highly emissive in the bluish-green color region with quantum yields of up to 87% in solid-state measurements.

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