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Photoswitchable Spiropyran Dyads for Biological Imaging

[Image: see text] The synthesis of a small-molecule dyad consisting of a far-red-emitting silicon rhodamine dye that is covalently linked to a photochromic spironaphthothiopyran unit, which serves as a photoswitchable quencher, is reported. This system can be switched reversibly between the fluoresc...

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Detalles Bibliográficos
Autores principales: Xiong, Yaoyao, Rivera-Fuentes, Pablo, Sezgin, Erdinc, Vargas Jentzsch, Andreas, Eggeling, Christian, Anderson, Harry L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010358/
https://www.ncbi.nlm.nih.gov/pubmed/27456166
http://dx.doi.org/10.1021/acs.orglett.6b01717
Descripción
Sumario:[Image: see text] The synthesis of a small-molecule dyad consisting of a far-red-emitting silicon rhodamine dye that is covalently linked to a photochromic spironaphthothiopyran unit, which serves as a photoswitchable quencher, is reported. This system can be switched reversibly between the fluorescent and nonfluorescent states using visible light at wavelengths of 405 and 630 nm, respectively, and it works effectively in aqueous solution. Live-cell imaging demonstrates that this dyad has several desirable features, including excellent membrane permeability, fast and reversible modulation of fluorescence by visible light, and good contrast between the bright and dark states.