Abstract
Azobenzene-3,3’-dicarboxylic acid exists in photoisomerizable (E) and (Z)-forms. Deprotonation of the carboxylic acid groups from the (E)-form occurs simultaneously, whereas in the (Z)-form it occurs in a stepwise fashion. The mono anionic form of the (Z)-isomer acts as a glycosidase mimic that proceeds through a general acid-general base catalytic mechanism. This is the first example of a photoresponsive glycosidase mimic. © Partner Organisations 2014.
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CITATION STYLE
Samanta, M., Krishna, V. S. R., & Bandyopadhyay, S. (2014). A photoresponsive glycosidase mimic. Chemical Communications, 50(74), 10577–10579. https://doi.org/10.1039/c4cc03394a
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