Extreme complementarity in a macrocycle-tweezer complex

Full text not archived in this repository.

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Colquhoun, H.M., Zhu, Z. and Williams, D.J. (2003) Extreme complementarity in a macrocycle-tweezer complex. Organic Letters, 5 (23). pp. 4353-4356. ISSN 1523-7060 doi: 10.1021/ol035626j

Abstract/Summary

Interaction of a novel pyrene-based tweezer molecule with a macrocyclic ether-imide-sulfone results in formation of a strongly bound complex (K-a = 24 000 M-1) in which binding results not only from pi-pi stacking interactions involving pyrene units as donors and macrocyclic naphthalene-tetracarboximide and biphenylenedisulfone groups as acceptors but also from N-(HO)-O-... and C-(HO)-O-... hydrogen bonds and from "reverse" pi-stacking of the electron-poor isophthaloyl residue of the tweezer with an electron-rich 3-aminophenoxy residue of the macrocyclic imide.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/11152
Identification Number/DOI 10.1021/ol035626j
Refereed Yes
Divisions Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
Uncontrolled Keywords PI-ASSOCIATED <2>CATENANES, MOLECULAR TWEEZERS, RECOGNITION, ETHER, <2>PSEUDOROTAXANES, CATENANES, RECEPTORS, SWITCH, GUEST, RING
Download/View statistics View download statistics for this item

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar