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基于环金属化杂环铱(III)配合物的发光材料——物理化学研究。

Light-emitting materials from cyclometalated heteroleptic iridium(III) complexes--A physicochemical study.

机构信息

Department of Chemistry, Annamalai University, Annamalainagar 608002, Tamilnadu, India.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2012 Feb 15;87:119-25. doi: 10.1016/j.saa.2011.11.021. Epub 2011 Nov 18.

Abstract

Phosphorescent studies of 2-arylimidazole heteroleptic cyclometalated iridium(III) complexes with picolinic acid as the ancillary ligand were made. The observed experimental data reveal that these complexes possess dominantly (3)MLCT and (3)π-π* excited states and the solvent shift of these complexes is interpreted by Reichardt-Dimroth and Marcus solvent functions. The results are consistent with prior assignments on the absorption band to a metal-to-ligand charge transfer excited state associated with chelating ligand. Emission kinetic studies exploited that the radiative transition (k(r)) increases with increasing λ(em).

摘要

研究了以吡啶酸为辅助配体的 2-芳基咪唑杂环金属铱(III)配合物的磷光。观察到的实验数据表明,这些配合物主要具有(3)MLCT 和(3)π-π*激发态,并用 Reichardt-Dimroth 和 Marcus 溶剂函数解释了这些配合物的溶剂位移。这些结果与先前关于吸收带的分配一致,即与螯合配体相关的金属-配体电荷转移激发态。发射动力学研究表明,辐射跃迁(k(r))随 λ(em)的增加而增加。

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