Ultrafast charge transfer excited state dynamics in trifluoromethyl-substituted iridium(III) complexes

被引：21

作者：

Bevernaegie, Robin ^{[1
]}

Marcelis, Lionel ^{[1
]}

Moreno-Betancourt, Angelica ^{[2
]}

Laramee-Milette, Baptiste ^{[3
]}

Hanan, Garry S. ^{[3
]}

Loiseau, Frederique ^{[2
]}

Sliwa, Michel ^{[4
]}

Elias, Benjamin ^{[1
]}

机构：

[1] UCL, IMCN, Pl Louis Pasteur 1,Box L4-01-02, B-1348 Louvain La Neuve, Belgium

[2] Univ Grenoble Alpes, CNRS, UMR 5250, Dept Chim Mol, BP53, F-38041 Grenoble, France

[3] Univ Montreal, Dept Chim, Pavillon JA Bombardier,5155 Chemin Rampe, Montreal, PQ H3T 2B1, Canada

[4] Univ Lille, CNRS, UMR 8516, LASIR,Lab Spectrochim Infrarouge & Raman, F-59000 Lille, France

来源：

PHYSICAL CHEMISTRY CHEMICAL PHYSICS | 2018年 / 20卷 / 43期

关键词：

EMITTING ELECTROCHEMICAL-CELLS; IR(III) COMPLEXES; PHOSPHORESCENCE; LIGANDS; BLUE;

D O I：

10.1039/c8cp04265a

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

Time-resolved spectroscopy was exploited to gain new insights into the nature and dynamics of charge transfer excited states of bis-cyclometalated Ir(III) complexes. We showed that its dynamics is strongly influenced by the nature of the diimine ligand due to the existence of a ligand-ligand charge transfer process in the picosecond timescale. All the results are supported by DFT/TD-DFT calculations and spectroelectrochemistry.

引用

页码：27256 / 27260

页数：5

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