4.7 Article

New fluorescent probes based on gallium(III) corrole complexes for the recognition of hydrogen sulfide: A journey from solution to intracellular site

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DYES AND PIGMENTS
卷 216, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2023.111304

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Corroles; Gallium complexes; Hydrogen sulfide; Probes; Chemosensors

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In this study, three fluorescent probes were developed for the detection of hydrogen sulfide (H2S) using gallium (III) corrole complexes. The probes were designed with nitro groups at the beta-pyrrolic positions. The compounds CGa-NO2 and CGa-2NO2 showed response to H2S, while CGa-EtNO2 acted as a turn-off probe. Mechanistic studies revealed that H2S coordination with gallium(III) and reduction of nitro group to aminated corrole were involved in the interaction. The probes exhibited potential for ratiometric sensing of H2S in non-aqueous solutions and demonstrated response to H2S in HeLa cells.
In this work, three fluorescent probes for detection of hydrogen sulfide (H2S) where prepared based on gallium (III) corrole complexes bearing nitro groups at beta-pyrrolic positions. Two of the compounds selected, the 3-nitro5,10,15- tris(pentafluorophenyl)corrolatogallium(III)(pyridine) (CGa-NO2) and the 3,17-dinitro-5,10,15-tris (pentafluorophenyl)corrolatogallium(III)(pyridine) (CGa-2NO2) present one and two nitro groups directly linked to the beta-pyrrolic position. The third compound, the (E)-3-(2-nitroprop-1-en-1-yl)-5,10,15-tris(pentafluorophenyl)corrolatogallium(III)(pyridine) (CGa-EtNO2), has a carbon-carbon double bond spacer between the corrole unit and the nitro group. All these derivatives were obtained from 5,10,15-tris(pentafluorophenyl)corrolatogallium(III)(pyridine) (CGa). The precursor CGa and the derivative CGa-EtNO2 behaved as turn-OFF probes, while compound CGa-NO2 responded as a turn-ON probe in the presence of H2S in the pH range of 5-9. Mechanistic studies show that the interaction of H2S with the probes involves its coordination with gallium(III) and in some cases the reduction of the nitro group to a new aminated corrole. While the formation of the coordination complex with H2S is almost immediate, the kinetics of the reduction is slow. Interestingly, for CGaNO2 the two processes can be explored in a ratiometric sensing of H2S in a non-aqueous solution showing a good linearity over an extended concentration range (5-200 mu M). The response of the corroles to H2S in intracellular medium was studied in 2D cultured cells (HeLa).

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