荧光
锌
化学
齿合度
螯合作用
密度泛函理论
硫化氢
吡啶
配体(生物化学)
反应性(心理学)
组合化学
结晶学
计算化学
无机化学
受体
生物化学
药物化学
有机化学
晶体结构
医学
硫黄
物理
替代医学
病理
量子力学
作者
Maria Strianese,Stefano Brenna,G. Attilio Ardizzoia,Daniela Guarnieri,Marina Lamberti,Ilaria D’Auria,Claudio Pellecchia
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2021-01-01
卷期号:50 (46): 17075-17085
被引量:19
摘要
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-/H2S fluorescent sensors via a coordinative-based approach. To shed light on the species formed in solution when HS-/H2S 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 H2S in living cells.
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