Highly phosphorescent organopalladium() complexes with metal-metal-to-ligand charge-transfer excited states in fluid solutions
Dinuclear pincer-type cyclometalated Pd( ii ) complexes with foldable diacetylide ligands show crystallographically determined intramolecular Pd Pd contacts of 3.203-3.380 Å. In deoxygenated fluid solutions, these Pd( ii ) complexes are highly phosphorescent in the red region with emission quantum y...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2019-07, Vol.48 (28), p.1417-1421 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Dinuclear pincer-type cyclometalated Pd(
ii
) complexes with foldable diacetylide ligands show crystallographically determined intramolecular Pd Pd contacts of 3.203-3.380 Å. In deoxygenated fluid solutions, these Pd(
ii
) complexes are highly phosphorescent in the red region with emission quantum yields up to 48%, which has been ascribed to metal-metal-to-ligand charge-transfer (MMLCT) excited states in nature.
Making Pd(
ii
) brightly shining: mononuclear analogues are non-emissive, but folded dinuclear palladium(
ii
) diacetylide complexes phosphoresce from MMLCT excited states with quantum yields up to 48%. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c9dt02525a |