Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 3, Pages 287-288Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b818050d
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- Deutschen Akademie der Naturforscher Leopoldina ( [9901/8-158]
- ETH Zurich
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Detailed kinetic investigations of the most common photo-switchable spiropyran, 6-nitro-BIPS, reveal that hydrolytic decomposition of its merocyanine isomer limits its utility in aqueous buffer; however, simple replacement of the 6-nitro substituent with an 8-carboxylate yields a BIPS photoswitch that is potentially better suited for biological applications.
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