Dual-mode fluorescence switching of photochromic bisthiazolylcoumarin
01 natural sciences
0104 chemical sciences
DOI:
10.1039/c1cc16516j
Publication Date:
2011-11-22T09:36:12Z
AUTHORS (3)
ABSTRACT
Three new photochromic coumarins were synthesized. Fluorescence of the open form of 7-hydroxy-3,4-bisthiazolyl-coumarin increased to 1400% by changing the pH only slightly from 6.05 to 7.58. This was subsequently quenched to 1.5% of the maximum intensity at the UV photostationary state in water-methanol media.
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