Solution and solid-state electrochemiluminescence of a fac-tris(2-phenylpyridyl)iridium(III)-cored dendrimer

被引:22
|
作者
Reid, Ellen F. [1 ]
Burn, Paul L. [2 ]
Lo, Shih-Chun [2 ]
Hogan, Conor F. [1 ]
机构
[1] La Trobe Univ, La Trobe Inst Mol Sci, Dept Chem, Bundoora, Vic 3086, Australia
[2] Univ Queensland, Ctr Organ Photon & Elect, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
Electrochemiluminescence; Dendrimer; Ir(PPY)(3); Solid-state electrochemistry; ELECTROGENERATED CHEMILUMINESCENCE; CHARGE-TRANSPORT; PHOTOPHYSICAL PROPERTIES; IRIDIUM; COMPLEXES; CORE; ELECTROCHEMISTRY; GENERATION; DYNAMICS; CHLORIDE;
D O I
10.1016/j.electacta.2013.03.094
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The solution phase and solid-state electrochemistry and electrochemiluminescence (ECL) of an iridium(III) complex-cored dendrimeric analogue of Ir(ppy)(3), (G1plr), are reported. The solid-state electrochemistry and solid-state ECL of Ir(ppy)(3) itself is also described for the first time. In solution phase, the dendrimer displays greater immunity to oxygen quenching in photoluminescence (PL) experiments and exhibits greater ECL efficiency compared to the parent Ir(ppy)(3) core under the same conditions, despite a lower photoluminescence quantum yield. It is proposed that the dendrons which effectively shield the core from PL quenching interactions in the solid-state counteract the effects of parasitic side-reactions during the solution ECL experiments. Electroactive and ECL-active solid-state films of both Ir(ppy)(3) and G1plr were produced by drop-coating on boron doped diamond electrodes. Films of Ir(ppy)(3) produced stable co-reactant ECL. However, films of G1plr produced lower than expected ECL intensity. This was attributed to poorer charge transport and the lipophilicity of the film limiting the rate of interaction with the co-reactant required for formation of the excited state. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:72 / 77
页数:6
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