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A red to near-infrared fluorescent probe featuring a super large Stokes shift for light-up detection of endogenous H2S

机译:红色到近红外荧光探针,具有超大的斯托克斯转移,用于内源性H2S的升级检测

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摘要

In this work, a new reaction-based red to near-infrared (NIR) fluorescent turn-on probe for H2S was developed. This probe uses a readily prepared dicyanoisophorone as the fluorophore and a 2, 4-dinitrobenzenether with an ortho-aldehyde group as the reaction site. Upon addition of H2S, a fast nucleophilic addition of H2S to the aldehyde group and a following efficient intramolecular thiolysis of dinitrophenyl ether occurred, which leads to release the fluorophore and give a rapid NIR fluorescence turn-on response for H2S with a super large Stokes shift (244 nm). The fluorescence enhancement was found up to 105-fold and the detection limit was determined to be as low as 42 nM. Importantly, this probe shows high selectivity and sensitivity for H2S without interference from biothiols. Furthermore, NIR fluorescent imaging of exogenous and endogenous H2S in living cells with this probe was also successfully applied. All the results indicate that this probe is excellent and highly valuable.
机译:在这项工作中,开发了一种新的基于反应的RED到近红外线(NIR)的H2S荧光导通探针。 该探针使用易于制备的二氰基异佛酮作为荧光团和2,4-二硝基苯醚,用邻醛基团作为反应位点。 在加入H 2 S后,将H 2 S的快速亲核加入到醛基中,并发生了二硝基苯醚的有效分子内硫酸分解,导致荧光团释放出荧光团并给出H2S的快速荧光开启反应,具有超大的斯托克斯转变 (244纳米)。 荧光增强被发现高达105倍,测定检出限量低至42nm。 重要的是,该探针显示出H2S的高选择性和灵敏度,而不会从生物噻菌素干扰干扰。 此外,还成功地应用了具有该探针的生物细胞中外源性和内源H2S的NIR荧光成像。 所有结果表明该探头优异且非常有价值。

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