Using acetate anions to induce translational isomerization in a neutral urea-based molecular switch

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Abstract

Vying for urea: The translational isomerism of a neutral [2]rotaxane can be controlled in solution through the addition and removal of acetate anions. In the absence of acetate ions, the macrocyclic host recognizes a diphenylurea derivative; recognition of acetate ions by the urea-based station causes relocation of the macrocycle to another binding site (see picture). (Figure Presented). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

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Huang, Y. L., Hung, W. C., Lai, C. C., Liu, Y. H., Peng, S. M., & Chiu, S. H. (2007). Using acetate anions to induce translational isomerization in a neutral urea-based molecular switch. Angewandte Chemie - International Edition, 46(35), 6629–6633. https://doi.org/10.1002/anie.200702197

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