"Synthesis of octa-tailed calix[4]resorcinarenes and characterization o" by Yong Chun. Chen

Date of Award

1999

Publication Type

Master Thesis

Degree Name

M.Sc.

Department

Chemistry and Biochemistry

Keywords

Chemistry, Organic.

Supervisor

Datton, P.,

Rights

info:eu-repo/semantics/openAccess

Abstract

This project was focused on synthesis of octa-tailed calix[4]resorcinarenes functionalized with pendant alpha-(diethyl acetamide) or alpha-(methyl acetate), preparation of Langmuir films and Langmuir-Blodgett films of the calix[4]resorcinarenes, and characterization of these compounds in solution and the Langmuir-Blodgett films. The octa-tailed calix[4]resorcinarene was synthesized by the cyclooligomerization of resorcinol and alpha,alpha-dihexyl acetaldehyde under acid-catalyzed conditions. The functionalized octa-tailed calix[4]resorcinarenes were obtained by substitution reaction with 2-bromo-NN-diethylacetamide or methyl bromoacetate under basic conditions. Langmuir films of the octa-tailed resorcin[4]arenes and their amide and ester derivatives were fabricated at the air/water interface. (Abstract shortened by UMI.)Dept. of Chemistry and Biochemistry. Paper copy at Leddy Library: Theses & Major Papers - Basement, West Bldg. / Call Number: Thesis1999 .C44. Source: Masters Abstracts International, Volume: 39-02, page: 0513. Adviser: P. Datton. Thesis (M.Sc.)--University of Windsor (Canada), 1999.

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