Spiropyrans bearing an N-alkylcarboxylate tether are a common structure in dynamic, photoactive materials and serve as colourimetric/fluorimetric cation receptors. In this study, we describe an efficient synthesis of spiropyrans with 2–12 carbon atom alkylcarboxylate substituents, and a systematic analysis of their interactions with metal cations using 1H NMR and UV-visible spectroscopy. All N-alkylcarboxyspiropyrans in this study displayed a strong preference for binding divalent metal cations and a modest increase in M2+ binding affinity correlated with increased alkycarboxylate tether length.
CITATION STYLE
Perry, A., & Kousseff, C. J. (2017). Synthesis and metal binding properties of N-alkylcarboxyspiropyrans. Beilstein Journal of Organic Chemistry, 13, 1542–1550. https://doi.org/10.3762/bjoc.13.154
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