Synthetic approaches introduce gold functionalities onto blue-phosphorescent complexes, preserving key properties.
In this work, we present synthetic approaches to introduce two gold-containing functionalities onto blue-phosphorescent trans -bis(acyclic diaminocarbene) platinum(II) acetylide complexes via carbon–gold σ-bond formation. The first strategy described involves transmetalation between a protected boronic ester and a gold(I)-phosphine or gold(I)-NHC source to form a Au–C aryl bond on the periphery of each phenylacetylide ligand. The second strategy employs diynyl acetylide ligands as bridging ligands, which forms new Au–C alkynyl bonds upon reaction with gold(I)-phosphine precursors in the presence of base. In total, seven gold-containing platinum acetylide complexes were accessed by these routes. Structural characterization by NMR in solution and X-ray crystallography in the solid state confirms successful incorporation of two gold-containing functionalities while preserving the Pt–C bonds of the acetylide ligands. Photophysical studies reveal that blue phosphorescence is preserved in these trimetallic Au–Pt–Au complexes, with photoluminescence spectra in 2 wt % PMMA bearing strong similarity to those of their corresponding gold-free complexes. Photoluminescence quantum yields of 0.13–0.29 are observed in blue-phosphorescent analogues with Au–C aryl linkages, dropping to 0.079 and 0.091 in the green-phosphorescent diynyl versions with Au–C alkynyl linkages.
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Dang et al. (2026) studied this question.
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