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• W3137416095 abstract "With the aim of developing a new fluorescence dye with enhanced photophysical properties, this study describes the modification of the 2-phenylsulfanylhydroquinone dimer to realize a new bioimaging molecule. The characteristics of the dimer were advanced by introducing tetraethylene glycol side chains to provide sufficient water solubility and a tether consisting of an N-hydroxysuccinimide-terminated C6-carbon chain to attach bioactive molecules. Two derivatives containing two or three tetraethylene glycol side chains were designed and prepared, and the latter showed sufficient water solubility for biochemical applications. Both compounds exhibited similar photophysical properties and blue fluorescence under UV light irradiation. The dye containing three tetraethylene glycol units reacted with bovine serum albumin in water to give fluorescent derivatives." @default.
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• W3137416095 date "2021-03-23" @default.
• W3137416095 modified "2023-10-12" @default.
• W3137416095 title "Development of Water Solubility of 2-Phenylsulfanylhydroquinone Dimer Dye" @default.
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• W3137416095 doi "https://doi.org/10.1021/acsomega.1c00703" @default.
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