Investigation of Luminescent Triplet States in Tetranuclear Cu<sup>I</sup> Complexes: Thermochromism and Structural Characterization
Pit Boden, Patrick Di Martino‐Fumo, Jasmin M. Busch, Florian R. Rehak, Sophie T. Steiger, Olaf Fuhr, Martin Nieger, Daniel Volz, Willem Klopper, Stefan Bräse, Markus Gerhards
Abstract
Abstract To develop new and flexible Cu I containing luminescent substances, we extend our previous investigations on two metal‐centered species to four metal‐centered complexes. These complexes could be a basis for designing new organic light‐emitting diode (OLED) relevant species. Both the synthesis and in‐depth spectroscopic analysis, combined with high‐level theoretical calculations are presented on a series of tetranuclear Cu I complexes with a halide containing Cu 4 X 4 core (X=iodide, bromide or chloride) and two 2‐(diphenylphosphino)pyridine bridging ligands with a methyl group in para (4‐Me) or ortho (6‐Me) position of the pyridine ring. The structure of the electronic ground state is characterized by X‐ray diffraction, NMR, and IR spectroscopy with the support of theoretical calculations. In contrast to the para system, the complexes with ortho ‐substituted bridging ligands show a remarkable and reversible temperature‐dependent dual phosphorescence. Here, we combine for the first time the luminescence thermochromism with time‐resolved FTIR spectroscopy. Thus, we receive experimental data on the structures of the two triplet states involved in the luminescence thermochromism. The transient IR spectra of the underlying triplet metal/halide‐to‐ligand charge transfer ( 3 M /XLCT) and cluster‐centered ( 3 CC) states were obtained and interpreted by comparison with calculated vibrational spectra. The systematic and significant dependence of the bridging halides was analyzed.