Strategic design and synthesis of osmium(II) complexes bearing a single pyridyl azolate π-chromophore: Achieving high-efficiency blue phosphorescence by localized excitation

Yi Ming Cheng, Elise Y. Li, Gene Hsiang Lee, Pi Tai Chou*, Sue Yi Lin, Ching Fong Shu, Kwun Chi Hwang, Yao Lun Chen, Yi Hwa Song, Yun Chi

*此作品的通信作者

研究成果: 雜誌貢獻期刊論文同行評審

55 引文 斯高帕斯(Scopus)

摘要

We present the strategic design and synthesis of Os(II) complexes bearing a single pyridyl azolate π-chromophore with an aim to attain high efficiency blue phosphorescence by way of localized transition. It turns out that our proposal of localized excitation seems to work well upon anchoring a single π-chromophore on the Os(II) complexes such that the control of MLCT versus ππ* (or even LLCT) transitions is more straightforward. Among the titled complexes, [Os(CO)3(tfa)(fppz)] (1) and [Os(CO) 3(tfa)(fbtz)] (5) (tfa = trifluoroacetate, (fppz)H = 3-(trifluoromethyl)-5-(2-pyridyl)pyrazole, and (fbtz)H = 3-(trifluoromethyl)-5- (4-tert-butyl-2-pyridyl)-1,2,4-triazole) give the anticipated blue phosphorescence with efficiencies of 0.26 (λmax = 460 nm) and 0.27 (λmax = 450 nm), respectively. For their halide analogues [Os(CO)3(X)(fppz)] (2, X = Cl; 3, X = Br; 4, X = I) and phosphine-substituted isomeric derivatives [Os(tfa)(fppz)(PPh 2Me)2(CO)] (6-8), the localization of the excitation energy seems to populate at certain vibrational modes with weak bonding strength and hence an associated shallow potential energy surface to induce a facile radiationless transition. Furthermore, their ancillary ligands play an important role in fine-tuning not only the energy gap but also the emission intensity, i.e., in manifesting the radiationless transition pathways. Our results clearly show that there is always a tradeoff upon varying the parameters in an aim to optimize the hue and efficiency of phosphorescence toward blue.

原文英語
頁(從 - 到)10276-10286
頁數11
期刊Inorganic Chemistry
46
發行號24
DOIs
出版狀態已發佈 - 2007 十一月 26

ASJC Scopus subject areas

  • 物理與理論化學
  • 無機化學

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