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Poly(ester‐acetals) from geometric isomers of methyl azelaaldehydate glycerol acetal

1970; Inderscience Publishers; Volume: 8; Issue: 2 Linguagem: Inglês

10.1002/pol.1970.150080214

1542-9350

Robert W. Lenz, R. A. Awl, W.R. Miller, E. H. Pryde,

Synthesis and properties of polymers

Abstract The glycerol acetal of methyl azelaaldehydate is an ω‐hydroxy ester that exists as a mixture of dioxolanyl and dioxanyl isomers, each having two geometric isomers. Each of the four isomers was isolated by chromatographic (gas–liquid and column) and fractionating (crystallization and distillation) methods. Structural assignments were made on the basis of nuclear magnetic resonance and infrared spectral data. Linear poly(ester‐acetals) were prepared from each of the cis and trans forms of the dioxanyl isomers and from a mixture of the dioxolanyl geometric isomers. Physical properties of these polymers were correlated with their structures. When prepared with basic condensation catalysts, the polymers retained the geometric configuration and structural identity of the monomer. When prepared with lead acetate, structural rearrangement as well as polycondensation occurred, resulting in an enrichment of the dioxolanyl isomer and simultaneous increase in polymer crystallinity. The enrichment took place at elevated temperatures and also, unexpectedly, at room temperature upon long standing of the polymer. Isomer redistribution at room temperature appears to be antithermodynamic in the reaction sense, yielding a polymer of unusually high dioxolanyl unit content. The driving force for this isomerization may be crystallization of these units by a phenomenon termed a “crystallization‐induced reaction.”