Literature DB >> 28485818

Modulation of Bambusuril Anion Affinity in Water.

Vaclav Havel1,2, Michal Babiak1,3, Vladimir Sindelar1,2.   

Abstract

Neutral and negatively charged anion receptors functioning in pure water are rare in supramolecular chemistry. Moreover, studies on adjusting the affinity of such receptors toward anions in water are absent from the literature. Two new bambusurils, 1 a and 2 a, were prepared to demonstrate that the affinity of bambusurils towards anions can be altered by the length of carboxyalkyl groups attached to the macrocycles. The stability of the bambusuril complexes was further controlled by the pH value. The crystal structure of bambusuril 1 a was described, in which two carboxyalkyl arms fold into the macrocycle cavity, thus forming the intramolecular self-inclusion complex.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  anion recognition; bambusurils; macrocycles; self-assembly; supramolecular chemistry

Year:  2017        PMID: 28485818     DOI: 10.1002/chem.201701316

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

Review 1.  When Molecules Meet in Water-Recent Contributions of Supramolecular Chemistry to the Understanding of Molecular Recognition Processes in Water.

Authors:  Stefan Kubik
Journal:  ChemistryOpen       Date:  2022-04       Impact factor: 2.630

2.  Correlating Solution- and Solid-State Structures of Conformationally Flexible Resorcinarenes: Significance of a Sulfonyl Group in Intramolecular Self-Inclusion.

Authors:  Małgorzata Pamuła; Maija Nissinen; Kaisa Helttunen
Journal:  Chemistry       Date:  2020-04-30       Impact factor: 5.236

Review 3.  The Chaotropic Effect as an Assembly Motif in Chemistry.

Authors:  Khaleel I Assaf; Werner M Nau
Journal:  Angew Chem Int Ed Engl       Date:  2018-09-27       Impact factor: 15.336

  3 in total

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