SYNTHESIS AND REACTIONS OF TRIHALOMETHYL GROUP SUBSTITUTED ELECTRON-DEFICIENT OLEFINS.
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Author
HEDRICK, STEVEN THOMAS.Issue Date
1983Keywords
Alkenes.Polymers.
Polymerization.
Electron donor-acceptor complexes.
Carbenes (Methylene compounds)
Advisor
Hall, H. K.
Metadata
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The University of Arizona.Rights
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.Abstract
The reactions of five trihalomethyl group substituted electron-deficient olefins with electron-rich olefins were studied in order to determine the effect of steric bulk upon the subsequent reactions of the tetramethylene intermediates initially formed. Reactions of β-trihalomethyl group substituted olefins yielded cyclobutane adducts, resulting from a gem dimethyl effect which accelerates the collapse of the tetramethylene intermediate. Reactions of α-trihalomethyl group substituted olefins gave both small molecule and polymeric products. Polymers were produced in reactions where steric interactions between the termini of the tetramethylene intermediates prevented ring formation. Ester substituted electron-deficient olefins reacted with electron-rich olefins to give both cyclobutane and 6-alkoxy-3,4-dihydro-2H-pyran derivatives. A transition from concerted to stepwise reaction was observed, resulting from steric hindrance in the transition state leading to [4+2] cycloaddition. Exploratory studies of ion-radical propagation and chain transfer in polymerization processes were also conducted. The acid catalyzed free radical polymerization of imines was attempted, along with chain transfer studies of zwitterion-radical intermediates.Type
textDissertation-Reproduction (electronic)
Degree Name
Ph.D.Degree Level
doctoralDegree Program
ChemistryGraduate College