Os(II) Phosphors with Near-Infrared Emission Induced by Ligand-to-Ligand Charge Transfer Transition

Jia-Ling Liao, Yun Chi*, Shih-Hung Liu, Gene-Hsiang Lee, Pi-Tai Chou*, Hao-Xiang Huang, Yu-De Su, Chih-Hao Chang*, Jin-Sheng Lin, Meu-Rurng Tseng

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

36 Citations (Scopus)

Abstract

Heating of Os3(CO)12 with 6 equiv of 2-(3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl) pyridine (fptzH) in refluxing diethylene glycol monomethyl ether, followed by sequential treatment with stoichiometric Me3NO and addition of PPhMe2, afforded two isomeric mixtures of red-emitting [Os(fptz)2(PPhMe2) 2] (1T and 1C), for which the notations T and C stand for the trans and cis-oriented fptz chelates, respectively. Alternatively, preparation of Os(II) complex using a 1:1 mixture of 5,5′-di(trifluoromethyl)-3,3′- di-1,2,4-triazole (dttzH2) and 2,2′-bipyridine (bpy), instead of fptzH, gave isolation of a mononuclear Os(II) complex [Os(bpy)(dttz)(CO) 2] (2) in moderate yield. Replacement of CO with PPhMe2 on 2 afforded near-infrared (NIR)-emitting Os(II) complex [Os(bpy)(dttz) (PPhMe2)2] (3). The single-crystal X-ray structural analyses were executed on 1C, 2, and 3 to reveal the structural influence imposed by the various chelates. The photophysical and electrochemical properties were measured and discussed using the results of density functional theory (DFT) and time-dependent DFT calculations. Complex 3 is selected as the dopant to probe its electroluminescent properties by fabrication of the NIR emitting organic light-emitting diodes.
Original languageEnglish
Pages (from-to)9366-9374
JournalInorganic Chemistry
Volume53
Issue number17
Online published20 Aug 2014
DOIs
Publication statusPublished - 2 Sept 2014
Externally publishedYes

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