The cucurbit[n]uril family: prime components for self-sorting systems

J Am Chem Soc. 2005 Nov 16;127(45):15959-67. doi: 10.1021/ja055013x.

Abstract

We determined the values of Ka for a wide range of host-guest complexes of cucurbit[n]uril (CB[n]), where n = 6-8, using 1H NMR competition experiments referenced to absolute binding constants measured by UV/vis titration. We find that the larger homologues--CB[7] and CB[8]--individually maintain the size, shape, and functional group selectivity that typifies the recognition behavior of CB[6]. The cavity of CB[7] is found to effectively host trimethylsilyl groups. Remarkably, the values of Ka for the interaction of CB[7] with adamantane derivatives 22-24 exceeds 10(12) M(-1)! The high levels of selectivity observed for each CB[n] individually is also observed for the CB[n] family collectively. That is, the selectivities of CB[6], CB[7], and CB[8] toward a common guest can be remarkably large. For example, guests 1, 3, and 11 prefer CB[8] relative to CB[7] by factors greater than 10(7), 10(6), and 3000, respectively. Conversely, guests 23 and 24 prefer CB[7] relative to CB[8] by factors greater than 5100 and 990, respectively. The high levels of selectivity observed individually and collectively for the CB[n] family renders them prime components for the preparation of functional biomimetic self-sorting systems.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biomimetic Materials / chemistry*
  • Bridged-Ring Compounds / chemistry*
  • Crystallography, X-Ray
  • Imidazoles / chemistry*
  • Molecular Structure

Substances

  • Bridged-Ring Compounds
  • Imidazoles