Colorimetric enantiodiscrimination of alpha-amino acids in protic media

J Am Chem Soc. 2005 Jun 8;127(22):7986-7. doi: 10.1021/ja052029e.

Abstract

A new method is described for the determination of optical purity of alpha-amino acid samples in protic media. No derivatization of the analyte or multistep synthesis is required, and high accuracy is obtained from the colorimetric output. Chiral discrimination is achieved through the use of an optically pure trans-1,2-diaminocyclohexane-derived Cu(II)-containing host that differentiates amino acid enantiomers by a factor of about 2. Enantioselective signaling arises from the implementation of an indicator displacement assay based on competitive Cu(II) coordination involving the chiral Cu(II)-containing host, the amino acid guest, and a metal ion indicator. The molecular structure of the host/guest complex was determined by X-ray analysis and exhibits chelation of the Cu(II) center by the amino acid to provide substrate organization.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acids / analysis
  • Amino Acids / chemistry*
  • Colorimetry / methods*
  • Copper / chemistry
  • Crystallography, X-Ray
  • Cyclohexylamines / chemistry
  • Hydrophobic and Hydrophilic Interactions
  • Kinetics
  • Organometallic Compounds / chemistry
  • Solvents
  • Spectrophotometry, Ultraviolet
  • Stereoisomerism

Substances

  • Amino Acids
  • Cyclohexylamines
  • Organometallic Compounds
  • Solvents
  • Copper
  • 1,2-cyclohexanediamine