Characterization of Triplet State of Cyanine Dyes with Two Chromophores Effect of Molecule Structure

I. Borissevitch, P. J. Gonçalves, L. P. Ferreira, A. Kostyukov, V. Kuzmin
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Abstract

Quantum yields (φT) and energies (ET) of the first triplet state T1 for four molecules of cyanine dyes with two chromophores (BCDs), promising photoactive compounds for various applications, for example, as photosensitizers in photodynamic therapy (PDT) and fluorescence diagnostics (FD), were studied in 1-propanol solutions by steady-state and time-resolved optical absorption techniques. BCDs differ by the structure of the central heterocycle, connecting the chromophores. The heterocycle structure is responsible for electron tunneling between chromophores, for which efficiency can be characterized by splitting of the BCD triplet energy levels. It was shown that the increase in the tunneling efficiency reduces ET values and increases φT values. This aspect is very promising for the synthesis of new effective photosensitizers based on cyanine dyes with two interacting chromophores for various applications, including photodynamic therapy.
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分子结构双发色团效应下菁染料三重态的表征
采用稳态和时间分辨光学吸收技术,研究了具有两个发色团(bcd)的4个菁染料分子的第一三重态T1的量子产率(δ t)和能量(ET),这些化合物在光动力治疗(PDT)和荧光诊断(FD)中作为光敏剂具有各种应用前景。bcd的不同之处在于连接发色团的中心杂环的结构。杂环结构负责发色团之间的电子隧穿,其效率可以通过BCD三重态能级的分裂来表征。结果表明,掘进效率的提高降低了ET值,增大了φT值。这方面的研究为基于花青素染料和两个相互作用的发色团合成新型有效光敏剂提供了广阔的前景,可用于包括光动力治疗在内的各种应用。
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