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Preparation of a photostable tribrachia cyanine dye and its high chemical activity towards hydrosulfide

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Abstract The cyanine dye ( 1 ) with three arms of one chromenyl group and two indol groups was synthesized in this paper; and the proposed synthetic mechanism was also… Click to show full abstract

Abstract The cyanine dye ( 1 ) with three arms of one chromenyl group and two indol groups was synthesized in this paper; and the proposed synthetic mechanism was also mentioned. It has excellent photostability compared to three typical cyanine dyes. Dye 1 gives high chemical activity and nearly turn-on fluorescent response towards hydrosulfide at 600–800 nm, it also has good selectivity towards hydrosulfide over other species; the detection reaction mechanism was proved by 1 H NMR analysis, and the emission responses was elucidated by time dependent density functional theory (TDDFT) calculation. The in cellular fluorescent imaging application of the dye 1 was successfully performed for the hydrosulfide imaging of HeLa cells.

Keywords: cyanine dye; towards hydrosulfide; high chemical; dye; chemical activity

Journal Title: Dyes and Pigments
Year Published: 2018

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