- Synthesis and photochemistry of pH-sensitive GFP chromophore analogs
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GFP chromophore analogs (7a-e, 8, and 10a,b) containing 2-thienyl-, 5-methyl-2-furyl-, 2-pyrryl, and 6-methyl-2-pyridyl-groups were synthesized and their fluorescence spectra recorded in the pH range 1-7. NMR studies showed that protonation of 8 (2-thieny
- Katritzky, Alan R.,Yoshioka-Tarver, Megumi,El-Gendy, Bahaa El-Dien M.,Hall, C. Dennis
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supporting information; experimental part
p. 2224 - 2227
(2011/05/05)
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- Excited-state intramolecular proton transfer molecules bearing o -hydroxy analogues of green fluorescent protein chromophore
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o-Hydroxy analogues, 1a-g, of the green fluorescent protein chromophore have been synthesized. Their structures and electronic properties were investigated by X-ray single-crystal analyses, electrochemistry, and luminescence properties. In solid and nonpo
- Chuang, Wei-Ti,Hsieh, Cheng-Chih,Lai, Chin-Hung,Lai, Cheng-Hsuan,Shih, Chun-Wei,Chen, Kew-Yu,Hung, Wen-Yi,Hsu, Yu-Hsiang,Chou, Pi-Tai
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scheme or table
p. 8189 - 8202
(2011/12/04)
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