Date of Award
Chemistry and Biochemistry
CC BY-NC-ND 4.0
This project was focused on synthesis of octa-tailed calixresorcinarenes functionalized with pendant alpha-(diethyl acetamide) or alpha-(methyl acetate), preparation of Langmuir films and Langmuir-Blodgett films of the calixresorcinarenes, and characterization of these compounds in solution and the Langmuir-Blodgett films. The octa-tailed calixresorcinarene was synthesized by the cyclooligomerization of resorcinol and alpha,alpha-dihexyl acetaldehyde under acid-catalyzed conditions. The functionalized octa-tailed calixresorcinarenes were obtained by substitution reaction with 2-bromo-NN-diethylacetamide or methyl bromoacetate under basic conditions. Langmuir films of the octa-tailed resorcinarenes 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.
Chen, Yong Chun., "Synthesis of octa-tailed calixresorcinarenes and characterization of Langmuir-Blodgett films on these compounds." (1999). Electronic Theses and Dissertations. 3702.