Skip to main navigation Skip to search Skip to main content

Cucurbit[8]uril rotaxanes

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

The synthesis of [2]rotaxanes, each comprising a viologen core threaded through a cucurbit[8]uril (Q8, Figure 1) macrocycle and stoppered by tetraphenylmethane groups, and their binding to second guests as inclusion complexes in organic and aqueous media are described. Stoppering was observed to have little effect on binding. Chemical modification of the threaded guest was used to control solubility and binding characteristics, thus demonstrating a novel approach to making artificial receptors with readily modifiable properties.

Original languageEnglish
Pages (from-to)4898-4901
Number of pages4
JournalOrganic Letters
Volume13
Issue number18
DOIs
StatePublished - Sep 16 2011

Fingerprint

Dive into the research topics of 'Cucurbit[8]uril rotaxanes'. Together they form a unique fingerprint.

Cite this