The Syntheses of Novel Indicators and Materials for Chiral Separation

by Johnson, Rolanda

Abstract (Summary)
The colorimetric properties of resorcinarene solutions had not been fully investigated since von Baeyer's initial synthesis. We find that the solutions containing resorcinarene macrocycles develop color upon heating or standing. In the presence of saccharides, these solutions exhibit significant color changes which are readily observable by visual inspection. We determined that the solution color is due to macrocycle ring opening and oxidation. The optical responses to saccharides are due to complexation of the sugar with the acyclic chromophores. We have applied these mechanistic insights towards the challenging problems of the visual detection of saccharides and other important biologically analytes. In addition, we also report the first single crystal X-ray crystal structure determination of a rarely observed "diamond" resorcinarene stereoisomer. The visual sensing of saccharides is of importance to medical diagnostics and industry. The synthesis of the diamine tripod and the diamine fluorescein compounds will be presented and their application towards the detection of saccharides and biomolecules of interest will be discussed. In addition to this, the synthesis of a new cationic chiral surfactant, the l-arginine methyl ester, for use in chiral separations will also be presented.
Bibliographical Information:

Advisor:Warren Johnson; Robert Strongin; Bill Crowe; Steven Watkins; William Daly

School:Louisiana State University in Shreveport

School Location:USA - Louisiana

Source Type:Master's Thesis



Date of Publication:01/15/2004

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