A versatile template for the formation of [2]pseudorotaxanes. 1,2-Bis(pyridinium)ethane axles and 24-crown-8 ether wheels
- 6 January 2006
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 4 (4) , 667-680
- https://doi.org/10.1039/b514528g
Abstract
Linear 1,2-bis(pyridinium)ethane ‘axles’ and macrocyclic 24-membered crown ether ‘wheels’ (24C8, DB24C8 and DN24C8) combine to form [2]pseudorotaxanes. These interpenetrated adducts are held together by N+⋯O ion-dipole interactions, a series of C–H⋯O hydrogen bonds and π-stacking between electron-poor pyridinium rings of the axle and electron-rich catechol rings of the wheel. 1H NMR spectroscopy was used to identify the structural details of the interaction and to determine the thermodynamics of the binding process in solution. Analysis of nine of these adducts by single crystal X-ray crystallography allowed a detailed study of the non-covalent interactions in the solid state. A wide variety of structural changes could be made to the system. The versatility and potential of the template for the construction of permanently interlocked structures such as rotaxanes and catenanes is discussed.Keywords
This publication has 76 references indexed in Scilit:
- C–H⋯O and other weak hydrogen bonds. From crystal engineering to virtual screeningChemical Communications, 2005
- Metal–Organic Rotaxane Frameworks: Three‐Dimensional Polyrotaxanes from Lanthanide‐Ion Nodes, Pyridinium N‐Oxide Axles, and Crown‐Ether WheelsAngewandte Chemie International Edition in English, 2005
- Threading/dethreading processes in pseudorotaxanes. A thermodynamic and kinetic studyNew Journal of Chemistry, 2004
- Molecular Shuttles by the Protecting Group ApproachThe Journal of Organic Chemistry, 2000
- [2]Rotaxane molecular shuttles employing 1,2-bis(pyridinium)ethane binding sites and dibenzo-24-crown-8 ethersChemical Communications, 2000
- Rotaxane or Pseudorotaxane? That Is the Question!Journal of the American Chemical Society, 1998
- Dialkylammonium Ion/Crown Ether Complexes: The Forerunners of a New Family of Interlocked MoleculesAngewandte Chemie International Edition in English, 1995
- Enthalpically driven cyclophane-arene inclusion complexation: solvent-dependent calorimetric studiesJournal of the American Chemical Society, 1991
- Chemistry of synthetic receptors and functional group arrays. 15. The effects of added water on thermodynamic aspects of hydrogen bond based molecular recognition in chloroformJournal of the American Chemical Society, 1991
- Complexation of Paraquat by a bisparaphenylene-34-crown-10 derivativeJournal of the Chemical Society, Chemical Communications, 1987