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NIR-emissive erbium-quinolinolate complexes

机译:近红外发射-喹啉配合物

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摘要

Studies addressed to a deep understanding of the structure/property relationship on the near infrared (NIR)-emissive erbium-quinolinolate complexes, which are of interest for low-cost photonic systems, are reviewed. The role of the 8-quinolinolate ligand (Q), which studies also as sensitizer to overcome the weak absorptivity of lanthanide ion, is discussed. Synthetic and structural aspects are reported to revise the old assumption that these complexes are analogous in structure to AlO_3 and to point out the specificity of the lanthanide coordination chemistry, in fact depending on reaction conditions, species with high coordination numbers and differing for nuclearity and stoichiometry have been isolated and fully characterized. In some instances it has been shown that coordinated water molecules directly bounded to the emitting erbium ion definitely represent the most effective quenchers for the luminescence at 1.5 μm. Additionally, the combined opticaland structural investigationofwater-free Er-quinolinolate complexes, allows one to conclude that the C-H groups sitting in the Er~(3+) inner coordination sphere represent a very severe limit to the near-infrared emission yield. Implementation of structural/spectroscopic data into a theoretical model based on F6rster's energy transfer resonant theory provides a comprehensive analysis of the near infrared emission quenching in erbium complexes useful to predict the quenching effects in luminescent lanttianide-complexes from the measurements of the vibrational absorption spectrum of the compound, the lanthanide radiative lifetime, and the minimum distance between the emitting ion and the quenchers. On that basis, in order to significantly improve the near-infrared emission yield, ligands which do not bear NH, CH or OH groups at a distance shorter than 7-8 A from the emitting ion are required. At the same time high sensitization efficiency of near-infrared emission and population saturation of trivalent erbium is achieved in these complexes, photoexcited into the absorption band of the quinolinolate sensitizer. It is concluded that a fully halogenated quinolinolate ligand can be an optimal candidate to improve the luminescent properties of erbium complexes.
机译:综述了对深入研究低成本光子系统感兴趣的近红外(NIR)-发射性-喹啉醇配合物的结构/性质关系的研究。讨论了8-喹啉酸酯配体(Q)的作用,该配体也作为敏化剂克服了镧系元素离子的弱吸收性。据报道,在合成和结构方面修改了这些复合物在结构上类似于AlO_3的旧假设,并指出了镧系元素配位化学的特异性,实际上取决于反应条件,具有高配位数的物种以及核和化学计量的不同已被隔离并具有完整特征。在某些情况下,已经证明直接结合到发射the离子上的配位水分子无疑代表了在1.5μm处发光的最有效的猝灭剂。此外,对无水Er-喹啉酸酯配合物的光学和结构研究相结合,可以得出这样的结论:位于Er〜(3+)内部配位球中的C-H基团代表了对近红外发射量的非常严格的限制。将结构/光谱数据应用于基于F6rster能量转移共振理论的理论模型中,可以对analysis络合物中的近红外发射猝灭进行全面分析,可用于通过测量Lantianide络合物的振动吸收光谱来预测其发光猝灭作用。化合物,镧系元素的辐射寿命以及发射离子与猝灭剂之间的最小距离。在此基础上,为了显着提高近红外发射率,需要在距发射离子的距离短于7-8 A的距离内不带有NH,CH或OH基团的配体。同时,在这些被光激发进入喹啉醇酸酯敏化剂的吸收带中的配合物中,实现了近红外发射的高敏化效率和三价valent的种群饱和。结论是完全卤化的喹啉酸酯配体可以是改善配合物的发光性能的最佳候选者。

著录项

  • 来源
    《Coordination chemistry reviews》 |2011年第22期|p.2514-2529|共16页
  • 作者单位

    Dipartimento di Chimica Inorganica ed Analitica, Universita di Cagliari, S.S. 554-Bivia per Sestu. 109042 Monserrata-Cagliari, Italy;

    Dipartimento di Chimica Inorganica ed Analitica, Universita di Cagliari, S.S. 554-Bivia per Sestu. 109042 Monserrata-Cagliari, Italy;

    Dipartimento di Chimica Inorganica ed Analitica, Universita di Cagliari, S.S. 554-Bivia per Sestu. 109042 Monserrata-Cagliari, Italy;

    Dipartimento di Chimica Inorganica ed Analitica, Universita di Cagliari, S.S. 554-Bivia per Sestu. 109042 Monserrata-Cagliari, Italy;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    unthanides; erbium; luminescence; NIR; quinolinolates; coordination complexes;

    机译:than铒;发光近红外;喹啉酸酯配合物;
  • 入库时间 2022-08-18 03:00:54

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