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
Hauptverfasser: Lin, Jinqiang, Zou, Chao, Zhang, Xiaobao, Gao, Qin, Suo, Sa, Zhuo, Qihang, Chang, Xiaoyong, Xie, Mo, Lu, Wei
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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%.
ISSN:1477-9226
1477-9234
DOI:10.1039/c9dt02525a