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A Carbazole-Bridged Biscyclometalated Diplatinum Complex: Synthesis, Characterization, and Dual-Mode Aggregation-Enhanced Phosphorescence.

Authors :
Gong ZL
Tang K
Zhong YW
Source :
Inorganic chemistry [Inorg Chem] 2021 May 03; Vol. 60 (9), pp. 6607-6615. Date of Electronic Publication: 2021 Apr 16.
Publication Year :
2021

Abstract

A cationic carbazole-bridged biscyclometalated diplatinum complex 4 has been synthesized and characterized. Single-crystal X-ray analysis demonstrates that complex 4 displays a dimeric structure with noncovalent π-π stacking and unique double Pt-Pt interactions. In aerated dilute CH <subscript>3</subscript> CN, complex 4 is characterized by a very weak monomeric yellow emission (λ <subscript>emi</subscript> = 547 nm; Φ = 0.51%), which is attributed to the triplet intraligand ( <superscript>3</superscript> LC) excited state mixing with some charge transfer characters. In contrast, under aerated conditions, the dispersion of 4 in a mixed solvent of CH <subscript>3</subscript> CN/Et <subscript>2</subscript> O (1/9, v/v) or CH <subscript>3</subscript> CN/H <subscript>2</subscript> O (1/9, v/v) displays intense yellow (λ <subscript>emi</subscript> = 550 nm; Φ = 35.5%; τ = 11.10 μs) and red emission (λ <subscript>emi</subscript> = 635 nm; Φ = 14.1%; τ = 7.00 μs), respectively. These aggregation-induced phosphorescent emission enhancements are considered being caused by the oxygen-shielding effect and the molecular rigidification-induced decrease of nonradiative decays in the aggregate state. The morphology and size of the aggregates under these two conditions are examined by scanning electron microscope and dynamic light scattering analysis. The absorption and emission properties of 4 are further rationalized by time-dependent density functional theory calculations on a model compound.

Details

Language :
English
ISSN :
1520-510X
Volume :
60
Issue :
9
Database :
MEDLINE
Journal :
Inorganic chemistry
Publication Type :
Academic Journal
Accession number :
33861581
Full Text :
https://doi.org/10.1021/acs.inorgchem.1c00403