102913-32-6Relevant academic research and scientific papers
Synthesis and photochemistry of pH-sensitive GFP chromophore analogs
Katritzky, Alan R.,Yoshioka-Tarver, Megumi,El-Gendy, Bahaa El-Dien M.,Hall, C. Dennis
supporting information; experimental part, p. 2224 - 2227 (2011/05/05)
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
Excited-state intramolecular proton transfer molecules bearing o -hydroxy analogues of green fluorescent protein chromophore
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
scheme or table, p. 8189 - 8202 (2011/12/04)
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
