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Photoswitchable Spiropyran Dyads for Biological Imaging.
- Source :
-
Organic letters [Org Lett] 2016 Aug 05; Vol. 18 (15), pp. 3666-9. Date of Electronic Publication: 2016 Jul 26. - Publication Year :
- 2016
-
Abstract
- 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.
- Subjects :
- Benzopyrans chemical synthesis
Fluorescent Dyes chemical synthesis
Indoles chemical synthesis
Molecular Structure
Nitro Compounds chemical synthesis
Photochemical Processes
Rhodamines chemical synthesis
Benzopyrans chemistry
Cell Survival
Fluorescent Dyes chemistry
Indoles chemistry
Nitro Compounds chemistry
Optical Imaging methods
Rhodamines chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1523-7052
- Volume :
- 18
- Issue :
- 15
- Database :
- MEDLINE
- Journal :
- Organic letters
- Publication Type :
- Academic Journal
- Accession number :
- 27456166
- Full Text :
- https://doi.org/10.1021/acs.orglett.6b01717