Calixarene/azolium cyclophane hybrids: synthesis, structure and conformations

Valerie Hesler, Brian Skelton, Allan White, David Brown, Murray Baker

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)
293 Downloads (Pure)

Abstract

© Springer Science+Business Media Dordrecht 2015. The synthesis, structure, and conformational behaviour of three imidazolium cyclophanes that incorporate one or two 4-tert-butylphenol or 4-tert-butylanisole groups as meta-disubstituted linkers in the macrocycle is described. The cyclophanes containing anisole moieties adopt a cone conformation in the solid state, which, in solution, is not labile on the NMR timescale. The cyclophanes containing one or two phenol moieties adopt conformations other than the cone in the solid state and are labile in solution on the NMR timescale. The phenol cyclophanes are readily deprotonated, and structural and conformational studies for a variety of the associated cyclophanes are also reported.
Original languageEnglish
Pages (from-to)53-69
JournalJournal of Inclusion Phenomena and Macrocyclic Chemistry
Volume82
Issue number1
Early online date14 Mar 2015
DOIs
Publication statusPublished - Jun 2015

Fingerprint

Dive into the research topics of 'Calixarene/azolium cyclophane hybrids: synthesis, structure and conformations'. Together they form a unique fingerprint.

Cite this