Macrocyclic Hamilton-type receptors comprising a ferrocene pivot

Luca Pisciottani, Maxime Douarre, Brigitte Bibal, Clotilde Davies, Holly Roberts, Brice Kauffmann, Sarah L. Horswell, James H.R. Tucker, Nathan D. McClenaghan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

Synthetic hydrogen-bonding receptors are described, which incorporate a central electroactive ferrocene moiety grafted with two adjacent bis(amido)pyridine motifs and an aliphatic tether (14 and 18 methylene units for 1 and 2, respectively) completing the macrocycle. The crystallographic structure, barbiturate guest-binding studies and electrochemical data are provided for the more strongly-binding macrocycle 2.

Original languageEnglish
Pages (from-to)869-875
Number of pages7
JournalSupramolecular Chemistry
Volume30
Issue number10
Early online date17 Jan 2018
DOIs
Publication statusPublished - 3 Oct 2018

Keywords

  • barbiturate
  • ferrocene
  • Hamilton receptor
  • hydrogen-bonding
  • Macrocycle

ASJC Scopus subject areas

  • Chemistry(all)

Fingerprint

Dive into the research topics of 'Macrocyclic Hamilton-type receptors comprising a ferrocene pivot'. Together they form a unique fingerprint.

Cite this