Multichromophoric sugar for fluorescence photoswitching

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Abstract

A multichromophoric glucopyranoside 2 bearing three dicyanomethylenepyran (DCM) fluorophores and one diarylethene (DAE) photochrome has been prepared by Cu(I)-catalyzed alkyne-azide cycloaddition reaction. The fluorescence of 2 was switched off upon UV irradiation, in proportion with the open to closed form (OF to CF) conversion extent of the DAE moiety. A nearly 100% Förster-type resonance energy transfer (FRET) from all three DCM moieties to a single DAE (in its CF) moiety was achieved. Upon visible irradiation, the initial fluorescence intensity was recovered. The observed photoswiching is reversible, with excellent photo resistance. © 2014 Maisonneuve et al.

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Maisonneuve, S., Métivier, R., Yu, P., Nakatani, K., & Xie, J. (2014). Multichromophoric sugar for fluorescence photoswitching. Beilstein Journal of Organic Chemistry, 10, 1471–1481. https://doi.org/10.3762/bjoc.10.151

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