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Uniform polymer in synthetic polymer chemistry

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AbstractThe preparation of uniform polymers and their use in fundamental polymer chemistry are reviewed. A typical method of preparation is a combination of living polymerization and supercritical fluid chromatography separation. Synthetic uniform polymers allow us to solve ambiguous problems in polymer chemistry due to molecular weight distribution and are of significant importance for studies on structure–property relationships. A close inspection of an isotactic uniform chloral oligomer with a symmetrical chemical structure reveals that oligomers are the first examples of stable atropisomers of aldehyde oligomers and that their chiroptical properties are due only to their helical geometries. A molecular‐level understanding of the mechanism and stoichiometry of the association process of polymer molecules is possible only with uniform polymers, and stereocomplex formation between isotactic and syndiotactic poly(methyl methacrylate)s in acetone has vigorously been studied by size exclusion chromatography (SEC) and NMR. End‐functionalized uniform polymers have enabled us to prepare uniform polymer architectures, such as block, graft, comb, and star polymers. A uniform stereoblock poly(methyl methacrylate) with an isotactic (methyl methacrylate)46‐syndiotactic (methyl methacrylate)46 structure shows a single SEC peak in chloroform but three peaks in acetone, which are ascribable to intermolecularly and intramolecularly associated complexes and nonassociated molecules. A three‐arm star polymer with one isotactic chain and two syndiotactic chains shows a peculiar SEC behavior in acetone due to a braid type of intramolecular stereocomplex formation. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 416–431, 2004
Title: Uniform polymer in synthetic polymer chemistry
Description:
AbstractThe preparation of uniform polymers and their use in fundamental polymer chemistry are reviewed.
A typical method of preparation is a combination of living polymerization and supercritical fluid chromatography separation.
Synthetic uniform polymers allow us to solve ambiguous problems in polymer chemistry due to molecular weight distribution and are of significant importance for studies on structure–property relationships.
A close inspection of an isotactic uniform chloral oligomer with a symmetrical chemical structure reveals that oligomers are the first examples of stable atropisomers of aldehyde oligomers and that their chiroptical properties are due only to their helical geometries.
A molecular‐level understanding of the mechanism and stoichiometry of the association process of polymer molecules is possible only with uniform polymers, and stereocomplex formation between isotactic and syndiotactic poly(methyl methacrylate)s in acetone has vigorously been studied by size exclusion chromatography (SEC) and NMR.
End‐functionalized uniform polymers have enabled us to prepare uniform polymer architectures, such as block, graft, comb, and star polymers.
A uniform stereoblock poly(methyl methacrylate) with an isotactic (methyl methacrylate)46‐syndiotactic (methyl methacrylate)46 structure shows a single SEC peak in chloroform but three peaks in acetone, which are ascribable to intermolecularly and intramolecularly associated complexes and nonassociated molecules.
A three‐arm star polymer with one isotactic chain and two syndiotactic chains shows a peculiar SEC behavior in acetone due to a braid type of intramolecular stereocomplex formation.
© 2003 Wiley Periodicals, Inc.
J Polym Sci Part A: Polym Chem 42: 416–431, 2004.

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