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首页> 外文期刊>Dyes and Pigments >Influence of alkyl chain lengths on the properties of iridium(III)-based piezochromic luminescent dyes with triazole-pyridine type ancillary ligands
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Influence of alkyl chain lengths on the properties of iridium(III)-based piezochromic luminescent dyes with triazole-pyridine type ancillary ligands

机译:烷基链长对具有三唑-吡啶类辅助配体的铱(III)基压致变色发光染料性能的影响

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摘要

To investigate the relationship between structures and piezochromic luminescence behavior and to develop excellent materials for efficient light-emitting electrochemical cells, a series of iridium(III) complexes with different length of alkyl chains have been designed and synthesized.The results show that all complexes exhibit not only naked-eye visible and reversible piezochromic behavior, but chain length-dependent emission properties: the shorter the alkyl chain is, the more remarkable mechano-chromic behavior and higher recrystallization temperature will be. In light of powder X-ray diffrac-tometry and differential scanning calorimetric data, the interconversion between crystalline and amorphous states upon external stimuli is response for the present piezochromism. Additionally, these complexes show high quantum yields of 55-65% in neat films as well as excellent redox reversibility. Despite changed alkyl chains are introduced into these complexes, the negligible effect on emitting colors and excited-state characters of them in both solutions and neat films have been observed. Such photophysical properties are also interpreted with the help of theoretical calculations. Moreover, the theoretical results suggest that the intrinsic intramolecular π-π stacking confirmed by the crystal structures can effectively restrict the opening of the structures in metal-centered excited-state, demonstrating their stability. The structure-property relationships and the results demonstrated here will help researchers develop and design more promising iridium(III)-based piezochromic materials and attractive phosphors for optical devices.
机译:为了研究结构与压致变色发光行为之间的关系,并开发出用于高效发光电化学电池的优异材料,设计并合成了一系列具有不同烷基链长度的铱(III)配合物。不仅肉眼可见和可逆的变色行为,而且取决于链长的发射特性:烷基链越短,机械变色行为越显着,重结晶温度越高。根据粉末X射线衍射法和差示扫描量热数据,在外部刺激下晶态和非晶态之间的相互转换是对当前压致变色的响应。此外,这些络合物在纯净薄膜中显示出55-65%的高量子产率以及出色的氧化还原可逆性。尽管在这些配合物中引入了烷基链变化,但在溶液和纯净薄膜中,它们的发色和激发态特性的影响可忽略不计。这种光物理性质也可以通过理论计算来解释。此外,理论结果表明,由晶体结构确认的固有分子内π-π堆积可以有效地限制处于以金属为中心的激发态的结构的开口,证明其稳定性。结构与性质的关系以及此处显示的结果将帮助研究人员开发和设计更有前途的基于铱(III)的压致变色材料和用于光学器件的有吸引力的磷光体。

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