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C–H Activation of Fluoroarenes: Synthesis, Structure, and Luminescence Properties of Copper(I) and Gold(I) Complexes Bearing 2‑Phenylpyridine Ligands

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posted on 03.03.2016, 00:00 by Roberto Molteni, Katharina Edkins, Martin Haehnel, Andreas Steffen
Although 2-phenylpyridine (ppy)-type complexes have been employed very successfully for the design of luminescent IrIII and PtII complexes, corresponding d10-coinage metal complexes are unknown. We report on the synthesis of the first, room-temperature-stable, CuI ppy-type complexes, by C–H activation of 2-(2,3,4,5-tetrafluorophenyl)­pyridine (Htfppy, 1) using [Cu­(OH)­(IDipp)] (2) (IDipp = bis­(2,6-di-isopropylphenyl)­imidazole-2-ylidene) or by lithiation of 1 and subsequent reaction with CuBr·SMe2 in the presence of a POP ligand (POP = bis­{2-(diphenyl­phosphanyl)­phenyl} ether) in THF, giving [Cu­(tfppy)­(IDipp)] (3) or [Cu­(tfppy)­(POP)] (4). The complexes thus obtained adopt distorted trigonal and tetrahedral coordination geometries, respectively. Gold­(I) tfppy complexes with IDipp (5) or PTol3 (6) ligands have also been prepared, showing a preference for linear coordination environments due to the noncoordinating pyridine moiety of the tfppy ligand. These structural differences have a profound effect on the photophysical properties of the coinage metal ppy compounds. The CuI tfppy complexes exhibit intense orange-red luminescence (λmax = 610 (3), 607 (4) nm) from a 3(intraligand)­CT state in the solid state at room temperature, with phosphorescence lifetimes of τ = 8.6 (3) and 9.5 (4) μs. In contrast, the linear coordination leads to weak emission of the AuI complexes, with 5 displaying simultaneous fluorescence and phosphorescence. Surprisingly, reaction of 2 with Htfppy (1) in MeCN leads to solvent activation and to isolation of a copper acetamide complex, [Cu­(N­(H)­C­(O)­Me)­(IDipp)] (14).

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