Takudrei

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The Halide Binding Behavior of 2-carbamoyl-7-ureido-1H-indoles: Conformational aspects

D. Makuc, Triyanti, M. Albrecht, J. Plavec, K. Rissanen, A. Valkonen, C. A. Schalley— 2009

Indole-based anion receptors with an carboxamide unit in 2- and an urea in 7-position were prepared and found to bind halides (as well as acetate and nitrate) in chloroform solutions at room temperature. Investigations of the binding behaviour show that the receptor is selective for chloride. Surprisingly, the truncated receptor 3 without the 2-carbamoyl substituent shows the highest affinity for Cl–. Thorough 1H, 13C and 15N NMR investigations indicate different binding modes for acetate, nitrate and halides to the receptor 2. The observation of a major conformational change of this receptor during the binding of the halide ions leads to an understanding of the relative binding affinities of 3 > 4 > 2 for chloride. The results of the NMR study are supported by ab initio calculations. In addition, ESI FTICR MS competition experiments of the indole 2 and the quinoline 1 reveal the “self-aggregation” of the receptors and show that halides have a higher affinity to 2 than to 1.

Title132
The Halide Binding Behavior of 2-carbamoyl-7-ureido-1H-indoles: Conformational aspects
AuthorD. Makuc, Triyanti, M. Albrecht, J. Plavec, K. Rissanen, A. Valkonen, C. A. Schalley
Date20090818
IdentifierDOI 10.1002/ejoc.200900721
Source(s)
CitationEur. J. Org. Chem. 2009, 4854-4866