Issue 19, 2019

Constructing bridged multifunctional calixarenes by intramolecular indole coupling

Abstract

2,2′-Bisindole units are suggested as new bridging motifs which can be easily created at calixarene cores. In TFA solutions, calix[4]arenes having pairs of indole groups originating from tryptamine or tryptophan residues are converted selectively into macrocycles bridged by indolylindoline moieties. The latter are easily transformed into fluorescent 2,2′-bisindole bridges upon oxidation. The coupling/oxidation sequence works fine at bridging the cavities of the cone and 1,3-alternate (thia)calix[4]arenes in their distal positions. Ester groups, triazole units and crown ether loops, which are practically important functionalities in calixarene chemistry, are compatible with the bridging strategy thus making available diverse calixarene-based hosts comprising novel features provided by the 2,2′-bisindole bridges. Of them the abilities to self-assembly and to bind anions through multiple hydrogen bonds were observed by X-ray crystallography, fluorescence measurements, and NMR experiments. When combined with a cation-binding site, the 2,2′-bisindole units can turn the calixarene molecules into heteroditopic receptors being able to stabilize the anionic parts of the ion pairs. This feature was assessed by using the 1,3-alternate calix[4]arene having the 2,2′-bisindole bridge and the crown-5-ether loop which was found to form neutral complexes with potassium acetate or potassium benzoate.

Graphical abstract: Constructing bridged multifunctional calixarenes by intramolecular indole coupling

Supplementary files

Article information

Article type
Research Article
Submitted
05 Ado 2019
Accepted
12 Hag 2019
First published
13 Hag 2019

Org. Chem. Front., 2019,6, 3327-3341

Constructing bridged multifunctional calixarenes by intramolecular indole coupling

B. Bolshchikov, S. Volkov, D. Sokolova, A. Gorbunov, A. Serebryannikova, I. Gloriozov, D. Cheshkov, S. Bezzubov, W. Chung, V. Kovalev and I. Vatsouro, Org. Chem. Front., 2019, 6, 3327 DOI: 10.1039/C9QO00859D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements