首页> 外文期刊>Synthesis and reactivity in inorganic, metal-organic, and nano-metal chemistry >Tuning the Emission Color of Cyclometalated Iridium ;Complex by Extending the pi-Electron Delocalization of the Aromatic Chromophore: Synthesis, Photophysical Properties, and X-Ray Crystal Structure
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Tuning the Emission Color of Cyclometalated Iridium ;Complex by Extending the pi-Electron Delocalization of the Aromatic Chromophore: Synthesis, Photophysical Properties, and X-Ray Crystal Structure

机译:调整环金属化铱的发射色;通过扩展芳香族发色团的π电子离域来实现复杂:合成,光物理性质和X射线晶体结构

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摘要

The authors report the preparation, crystal structure, and emission properties of Ir(btq)(2)(acac)(btq = 2-benzo[4,5-]thienylquinoline) (1). The compound has been characterised by UV-vis, fluorescence, MALDI-TOF, and H-1 and C-13 NMR spectroscopy. The crystal structure was also elucidated by X-ray diffraction methods. Its characteristics in terms of optical and structural properties are compared with the reported cyclometalated Ir(III) complex Ir(btp)(2)(acac) (2) (btp = 2-benzo[4,5-]thienylpyridine). Complex 1 shows 53 nm red-shift emission compared to the related complex 2.
机译:作者报告了Ir(btq)(2)(acac)(btq = 2-苯并[4,5-]噻吩基喹啉)的制备,晶体结构和发射性质(1)。该化合物已通过紫外可见,荧光,MALDI-TOF以及H-1和C-13 NMR光谱进行了表征。还通过X射线衍射方法阐明了晶体结构。将其在光学和结构性质方面的特性与已报道的环金属化Ir(III)配合物Ir(btp)(2)(acac)(2)(btp = 2-苯并[4,5-]噻吩基吡啶)进行了比较。与相关的络合物2相比,络合物1显示出53 nm的红移发射。

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