Binding Features of Molecular Clips. Separation of the Effects of Hydrogen Bonding and π−π Interactions
Journal of the American Chemical Society1997Vol. 119(42), pp. 9956–9964
Citations Over TimeTop 10% of 1997 papers
Joost N. H. Reek, A. Priem, Hans Engelkamp, Alan E. Rowan, Johannes A. A. W. Elemans, Roeland J. M. Nolte
Abstract
The ability of clip shaped molecules based on the building block diphenylglycoluril to form complexes with dihydroxybenzene guest molecules has been studied in detail. The binding strength of these complexes can be varied over a wide range (Ka ≈ 0−105 M-1), by applying small modifications in the host or the guest molecule. It is found that the complexation is a combination of different effects, viz., hydrogen bonding, π−π stacking interactions, and a cavity effect.
Related Papers
- → Crystal structures of dicarboxy-2,2′-bipyridyl complexes: the role of hydrogen bonding and stacking interactions(2004)49 cited
- → Weak interactions in barbituric acid derivatives. Unusually steady intermolecular organic “sandwich” complexes. π–π Stacking versus hydrogen bonding interactions(2007)7 cited
- → Hydrogen bonding and π–π stacking in hexaaquairon(II) bis(4′,7-dimethoxyisoflavone-3′-sulfonate) octahydrate(2005)2 cited
- → Hydrogen bonding and π–π stacking in 6-hydroxybiochanin A monohydrate(2006)1 cited
- → Displaced π–π stacking and hydrogen bonds in 3-bromo-N-(2-hydroxy-1,1-dimethylethyl)benzamide(2004)