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Polynuclear Cu4I4py4 complex loaded in mesoporous silica: Photophysics, theoretical investigation, and highly sensitive oxygen sensing application

机译:介孔二氧化硅中负载的多核Cu4I4py4络合物:光物理,理论研究和高灵敏度氧传感应用

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摘要

The polynuclear Cu4I4py4 complex has been largely studied in solution and in the powder form due to its interesting luminescent properties, which are largely dependent on temperature and pressure. In this work, we present the synthesis of the complex and its wet impregnation in a mesoporous silica host obtained by sol-gel methodology. For optimized guest loadings, the well-dispersed guest molecules exhibit strong interaction with molecular oxygen, resulting in a significant quenching of the luminescence. The process is highly reversible with a Stern-Volmer constant of Ksv = 33.8, which is the largest value found in the literature for similar complexes in the solid state, suggesting that the new material is a promising candidate for high sensitivity oxygen sensing. Density Functional Theory (DFT) and Time-Dependent DFT (TD-DFT) calculations reveal a weak intermolecular interaction between two guest complexes in the excited state, suggesting the formation of an excited state complex (excimer). The assumption of triplet excimer formation is confirmed by temperature- and concentration-dependent experiments, which provides a new way to explain the giant Stokes shift observed for the guest complex in different media.
机译:多核Cu4I4py4络合物由于其有趣的发光特性而在溶液和粉末形式中进行了大量研究,而发光特性在很大程度上取决于温度和压力。在这项工作中,我们介绍了复合物的合成及其在通过溶胶-凝胶法获得的介孔二氧化硅主体中的湿法浸渍。对于优化的客体负载,分散良好的客体分子表现出与分子氧的强烈相互作用,从而导致发光显着淬灭。该过程是高度可逆的,Stern-Volmer常数Ksv = 33.8,这是文献中固态相似配合物的最大值,表明该新材料是高灵敏度氧感测的有希望的候选者。密度泛函理论(DFT)和时变DFT(TD-DFT)计算显示出处于激发态的两个客体络合物之间的分子间相互作用较弱,表明形成了激发态络合物(准分子)。三重态受激准分子形成的假设已通过依赖温度和浓度的实验得以证实,这为解释在不同介质中观察到的客体复合物的巨大斯托克斯位移提供了新的方法。

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