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Synthesis of Polymeric Topological Isomers through Electrostatic Self-Assembly and Covalent Fixation with Star Telechelic Precursors

✍ Scribed by Yasuyuki Tezuka; Akiko Tsuchitani; Hideaki Oike


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
126 KB
Volume
25
Category
Article
ISSN
1022-1336

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✦ Synopsis


Abstract

Summary: A pair of macromolecular constitutional isomers having topologically distinctive, dicyclic constructions, that is, θ‐shaped and manacle‐shaped polymers, has been synthesized from a polymer self‐assembly, comprised of three‐armed star poly(tetrahydrofuran) [poly(THF)] having N‐phenylpyrrolidinium salt end groups carrying dicarboxylate counteranions (1S/2d). The presence of the two constitutional polymeric isomers was confirmed by means of a reversed‐phase liquid chromatography (RPC) technique. Moreover, size exclusion chromatography (SEC) showed that a major component possesses notably larger hydrodynamic volume than the others, and is assignable as a manacle‐shaped isomer while a minor component is assigned as a θ‐shaped isomer. The statistics of the covalent‐linking process of 1S/2d were consistent with the other experimental results.

An “electrostatic self‐assembly and covalent fixation” process of a trifunctional star‐shaped precursor gives rise to θ‐shaped and manacle‐shaped polymers.

imageAn “electrostatic self‐assembly and covalent fixation” process of a trifunctional star‐shaped precursor gives rise to θ‐shaped and manacle‐shaped polymers.


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Synthesis of Polymeric Topological Isome
✍ Yasuyuki Tezuka; Fuminobu Ohashi 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 115 KB

## Abstract **Summary:** An H‐shaped poly(tetrahydrofuran), poly(THF), having four terminal allyl groups was prepared through the covalent conversion of an ionically linked polymer assembly, comprised of four units of cationic poly(THF) having a pyrrolidinium salt and an allyl end group, and one un