We report the synthesis and characterization of tris(biphenyl-2,2'-diyl)metal complexes of trivalent group 9 elements (, M = Co, Rh, Ir) and their nonplanarly π-extended analogs, tris(1,1'-binaphthyl-2,2'-diyl)metal complexes (, M = Rh, Ir). Single crystal X-ray crystallography reveals the distorted octahedral geometry with an approximate symmetry of trianionic complexes (M = Co, Rh, Ir) and (M = Rh, Ir), which are contacted by three Li ions in the crystal. Complex exhibits yellow luminescence in THF with a photoluminescence quantum yield () of up to 0.73, along with a distinctive photophysical property, namely, a concentration dependence of the emission wavelength from 530 to 580 nm. This is a characteristic property of and has not been observed in its isoelectronic analog, tris(2-phenylpyridinato)iridium(III) (Ir(ppy)). The concentration-dependent optical properties originate from the dissociation equilibria of Li ions from the anionic chromophore. Complex also exhibits luminescence at 715 nm in THF, with a notable bathochromic shift from through the π-extension. The findings offer insights into the photophysical properties of homoleptic organo-transition metal complexes, providing the foundation for the design of related transition metal complexes.
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http://dx.doi.org/10.1021/acs.inorgchem.4c03514 | DOI Listing |
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