Abstract

Three new isomeric pyridone fluorenone hydrazone-based boron complexes, 3-BrN to 5-BrN, with bromination at the 3-, 4-, or 5-position of the pyridone ring and their corresponding σ-platinum complexes trans-Pt(PEt3)2(n-N)X (n = 3, 4, or 5; X = Cl, Br, I) resulting from oxidative addition of the aryl-Br bond of n-BrN to Pt(PEt3)2 and, for X = Cl, I, subsequent substitution of the halogenide ligand, were synthesized and characterized by NMR, UV–Vis absorption, and photoluminescence spectroscopy. The molecular structures of dyes 3-BrN to 5-BrN and of seven complexes, including the cis-isomer of the bromo complex resulting from 3-BrN, were established by single X-ray diffraction. The nearly orthogonal orientation of the Pt coordination plane with respect to the plane of the dye ligand limits intermolecular π-stacking interactions in the crystalline state while giving rise to extensive C-H···halogen and C-H···π interactions, resulting in intricate packing patterns. Electronic absorption spectra of dyes 3-BrN to 5-BrN show a prominent HOMO-LUMO absorption band at ca. 520 nm, which is red-shifted and intensifies on platination. All compounds are dual fluorescence and phosphorescence emitters in the range of 520 to 670 nm, or at ca. 1000 nm, both at room temperature and at 77 K. The population of an excited triplet state and their photostability even towards continuous light irradiation renders these compounds efficient sensitizers for singlet oxygen generation and catalysts for the photo-oxidation of triphenylphosphine.

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