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Homoleptic Alkynylphosphonium Au(I) Complexes as Push–Pull Phosphorescent Emitters

A series of compounds P1–P4 bearing terminal alkynyl sites connected with a phosphonium group via different π-conjugated linkers have been synthesized. The compounds themselves are efficient push–pull emitters and exhibit bright fluorescence in blue and near-UV regions. P1–P4 were used as alkynyl li...

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Bibliographic Details
Published in:Inorganic chemistry 2023-04, Vol.62 (13), p.5123-5133
Main Authors: Petrovskii, Stanislav, Paderina, Aleksandra, Sizova, Anastasia, Grachova, Elena
Format: Article
Language:English
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Summary:A series of compounds P1–P4 bearing terminal alkynyl sites connected with a phosphonium group via different π-conjugated linkers have been synthesized. The compounds themselves are efficient push–pull emitters and exhibit bright fluorescence in blue and near-UV regions. P1–P4 were used as alkynyl ligands to obtain a series of homoleptic bis-alkynyl Au­(I) complexes 1–4. The complexes demonstrate bright phosphorescence and dual emission with dominating phosphorescence (2–4). Terphenyl derivative complex 3 exhibits warm white emission in DMSO solution and pure white emission in PMMA films. Time-dependent density functional theory calculations have shown that the T1 excited state has a hybrid MLCT/ILCT nature with a dominant contribution of charge transfer across a ligand-centered “D-π-A” system. The variation of linker allows tuning the effect of intermolecular charge transfer and thus changing the electronic and photophysical properties of the organogold “D-π-A” system. The results presented unambiguously display the advances of the conception of organometallic “D-π-A” construction.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.2c04360