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基于咪唑并吡啶的锌(II)配合物作为荧光硫化氢探针。

Imidazo-pyridine-based zinc(II) complexes as fluorescent hydrogen sulfide probes.

机构信息

Dipartimento di Chimica e Biologia "Adolfo Zambelli", Università degli Studi di Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, SA, Italy.

Dipartimento di Scienza e Alta tecnologia, Università dell'Insubria and CIRCC, via Valleggio, 9, 22100 Como, Italy.

出版信息

Dalton Trans. 2021 Nov 30;50(46):17075-17085. doi: 10.1039/d1dt02489b.

Abstract

In this work we explore the interaction of HS with a family of fluorescent zinc complexes. In particular we selected a family of complexes with N,O-bidentate ligands aiming at assessing whether the zinc-chelating ligand plays a role in influencing the reactivity of HS with the complexes under investigation. Different experiments, performed by diverse spectroscopic techniques, provide evidence that HS binds the zinc center of all the complexes included in this study. The results highlight the potential of the devised systems to be used as HS/HS fluorescent sensors a coordinative-based approach. To shed light on the species formed in solution when HS/HS interacts with the title complexes and aiming to rationalize the photophysical properties of the sensing constructs, we performed a computational analysis based on the time dependent density functional theory (TD-DFT). Preliminary bio-imaging experiments were also performed and the results indicate the potential of this class of compounds as probes for the detection of HS in living cells.

摘要

在这项工作中,我们探索了 HS 与一系列荧光锌配合物的相互作用。特别是,我们选择了一系列具有 N,O-双齿配体的配合物,旨在评估锌螯合配体是否在影响研究中配合物与 HS 的反应性方面发挥作用。通过不同的光谱技术进行的不同实验提供了证据,表明 HS 结合了本研究中包含的所有配合物的锌中心。结果突出了设计系统作为 HS/HS 荧光传感器的潜力 - 基于配位的方法。为了阐明 HS/HS 与标题配合物相互作用时在溶液中形成的物种,并旨在合理化传感结构的光物理性质,我们进行了基于时间相关密度泛函理论(TD-DFT)的计算分析。还进行了初步的生物成像实验,结果表明该类化合物作为在活细胞中检测 HS 的探针具有潜力。

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