Cucurbit[8]uril forms tight inclusion complexes with cationic triamantanes-Reference-Cited by-同舟云学术

Cucurbit[8]uril forms tight inclusion complexes with cationic triamantanes

Published:2023 Issue:11 Volume:47 Page:5338-5346
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

King David¹,Šumanovac Tatjana²,Murkli Steven¹^ORCID,Schreiner Peter R.³^ORCID,Šekutor Marina²^ORCID,Isaacs Lyle¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, USA

2. Department of Organic Chemistry and Biochemistry, Ruđer Bošković Institute, Bijenička cesta 54, 10000, Zagreb, Croatia

3. Institute of Organic Chemistry, Justus Liebig University, Heinrich-Buff-Ring 17, 35392 Giessen, Germany

Abstract

Cationic triamantanes exhibit ultratight binding toward CB[7] and CB[8] as evidenced by 1H NMR spectroscopy, isothermal titration calorimetry, and computations.

Funder

University of Maryland

National Science Foundation

Hrvatska Zaklada za Znanost

U.S. Department of Education

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D3NJ00156C

Reference48 articles.

1. Cucurbituril chemistry: a tale of supramolecular success

2. Cucurbituril-Based Molecular Recognition

3. Can we beat the biotin–avidin pair?: cucurbit[7]uril-based ultrahigh affinity host–guest complexes and their applications

4. Acyclic Cucurbit[n]uril‐type Receptors: Preparation, Molecular Recognition Properties and Biological Applications

5. Structure and selectivity in host-guest complexes of cucurbituril

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