Remote control of anion binding by CH-based receptors
We show that the substitution of tetra(benzimidazole)resorcin[4]arenes with electron withdrawing groups on the upper rim enhances anion binding at the opposite edge by more than three orders of magnitude. Moreover, selective anion binding at either the OH/NH or CH binding sites is demonstrated. We s...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-03, Vol.6 (25), p.3417-342 |
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creator | Jurek, Paulina Szyma ski, Marek P Szumna, Agnieszka |
description | We show that the substitution of tetra(benzimidazole)resorcin[4]arenes with electron withdrawing groups on the upper rim enhances anion binding at the opposite edge by more than three orders of magnitude. Moreover, selective anion binding at either the OH/NH or CH binding sites is demonstrated.
We show that the substitution of tetra(benzimidazole)resorcin[4]arenes with electron withdrawing groups on the upper rim enhances anion binding at the opposite edge by more than three orders of magnitude. |
doi_str_mv | 10.1039/d3cc06038a |
format | Article |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Anions Aromatic compounds Binding sites Remote control |
title | Remote control of anion binding by CH-based receptors |
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