Author (Your Name)

Kevin J. Selby, Colby College

Date of Award

2005

Document Type

Honors Thesis (Open Access)

Department

Colby College. Chemistry Dept.

Advisor(s)

Jeffrey L. Katz

Second Advisor

Bradford P. Mundy

Abstract

Bicyclooxacalixarenes were synthesized in high yield via a selective, room temperature Sn Ar reaction of phluoroglucinol with 2,6-dichloropyridines. Functionality on the 2,6-dichloropyridioe was varied by changing the electron-withdrawing groups in the 3 and 5 positions (using chlorine, nitro groups, and cyano groups) and the side-chains in the 4-position (using ethyl, butyl, phenyl and ρ-tolyl groups). The resulting cage-like molecules were studied by X-ray crystallography and tested for metal complexation.

Keywords

Calixarenes, Synthesis, Aromatic compounds, Macrocyclic compounds

Included in

Chemistry Commons

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