Influence of gold nanostructures on excited state intramolecular proton transfer in multidomain HTTH dye

I. I. Hudzenko, A. Lopatynskyi, V. Chegel
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Abstract

Organic multidomain dyes exhibiting excited state intramolecular proton transfer (ESIPT) are known due to large Stokes shifts and dependence of their luminescence spectral characteristics on the properties of the environment. In this work, influence of gold nanostructures on the spectral characteristics of a “polycarbonate matrix – gold nanostructures – HTTH” system was studied using thiazole dye HTTH as an example. A hypothesis about the possibility of plasmon resonance energy transfer (PRET) between the HTTH molecules in different states, namely the ground state (enol form) and the state after proton transfer (keto form), mediated by gold nanostructures was experimentally tested. Presence of gold nanostructures in the vicinity of HTTH molecules was found to lead to the changes in the ratio of the luminescence peak intensities for the enol and keto form of these molecules. This phenomenon opens up the possibility of additional regulation of the spectral characteristics and may evidence the PRET effect in the systems containing ESIPT-exhibiting dyes and plasmonic nanostructures. The obtained results improve our understanding of the physical processes in the systems similar to the studied one and imply new practical applications of them such as fabrication of organic light-emitting diodes, sensors, super-resolution microscopy tools and ultraviolet-to-visible radiation convertors.
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金纳米结构对多域 HTTH 染料激发态分子内质子转移的影响
有机多畴染料表现出激发态分子内质子转移(ESIPT),由于其大的斯托克斯位移和其发光光谱特性依赖于环境的性质。本文以噻唑染料HTTH为例,研究了金纳米结构对“聚碳酸酯基质-金纳米结构- HTTH”体系光谱特性的影响。实验验证了金纳米结构介导HTTH分子在基态(烯醇态)和质子转移后态(酮态)两种不同状态之间发生等离子体共振能量转移(PRET)的可能性。发现在HTTH分子附近存在金纳米结构,导致这些分子的烯醇和酮形式的发光峰强度比发生变化。这一现象开启了对光谱特性进行额外调节的可能性,并可能在含有esipt表现的染料和等离子体纳米结构的系统中证明PRET效应。所得结果提高了我们对与所研究的系统相似的物理过程的理解,并暗示了它们在有机发光二极管、传感器、超分辨率显微镜工具和紫外-可见辐射转换器等制造方面的新的实际应用。
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