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Resorcinarenes are hexameric capsules in solution

Academic Article
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Overview

related to degree

  • Palmer, Liam C, Ph.D. in Chemistry, Scripps Research 1999 - 2005

authors

  • Evan-Salem, T.
  • Baruch, I.
  • Avram, L.
  • Cohen, Y.
  • Palmer, Liam C
  • Rebek Jr., Julius

publication date

  • 2006

journal

  • Proceedings of the National Academy of Sciences of the United States of America  Journal

abstract

  • The host-guest complexes of resorcin[4]arenes with small molecules in organic solutions are examined using modern NMR spectroscopic methods. The complexation of glutaric acid and beta-methyl d-glucopyranoside in chloroform were investigated through 2D COSY, 2D NOESY, 1D NOE, and diffusion-ordered NMR spectroscopy (DOSY) techniques. These methods indicate that the complex is a self-assembled capsule composed of six resorcinarenes that surround six guest molecules of glutaric acid or three molecules of beta-methyl d-glucopyranoside inside. The multiplicity of guest proton signals shows that the capsule provides an asymmetric magnetic environment that persists on the (1)H NMR time scale. The encapsulation of these guests and common solvents suggests that the phenomenon of reversible encapsulation in chemistry may be a century old.

subject areas

  • Calixarenes
  • Glutarates
  • Models, Molecular
  • Molecular Conformation
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Phenylalanine
  • Solvents
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Research

keywords

  • diffusion spectroscopy
  • encapsulation
  • self-assembly
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Identity

PubMed Central ID

  • PMC1567874

International Standard Serial Number (ISSN)

  • 0027-8424

Digital Object Identifier (DOI)

  • 10.1073/pnas.0604757103

PubMed ID

  • 16894154
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Additional Document Info

start page

  • 12296

end page

  • 12300

volume

  • 103

issue

  • 33

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