## Abstract **Summary:** Star‐shaped hydroxy‐terminated poly(__ε__‐caprolactone)s (__ss__PCL), with arms of different lengths, were obtained by ring‐opening polymerization (ROP) of __ε__‐caprolactone initiated by pentaerythritol, and were condensed with __α__‐methyl‐__ω__‐(3‐carboxypropionyloxy)‐po
Well-Defined Miktocycle Eight-Shaped Copolymers Composed of Polystyrene and Poly(ε-caprolactone): Synthesis and Characterization
✍ Scribed by Gang-Yin Shi; Jiao-Tong Sun; Cai-Yuan Pan
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 607 KB
- Volume
- 212
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
A series of well‐defined miktocycle number‐eight‐shaped copolymers composed of cyclic polystyrene (PS) and cyclic poly(ε‐caprolactone) (PCL) have been successfully synthesized by a combination of atom transfer radical polymerization (ATRP), ring‐opening polymerization (ROP), and “click” reaction. The synthesis involves three steps: 1) preparation of tetrafunctional initiator with two acetylene groups, one hydroxyl group and a bromo group; 2) preparation of two azide‐terminated block copolymers, N~3~‐PCL‐(CHC)~2~‐PS‐N~3~, with two acetylene groups anchored at the junction; and 3) intramolecular cyclization of the block copolymer through “click” reaction under high dilution. The ^1^H NMR, FT‐IR, and gel permeation chromatography (GPC) techniques are applied to characterize the chemical structures of the resulting intermediates and the target polymers. Their thermal behavior is investigated by differential scanning calorimeter (DSC). The decrease in chain mobility of eight‐shaped copolymers restricts the crystallization of PCL. magnified image
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## Abstract **Summary:** Well‐defined star‐shaped poly(__ε__‐caprolactone)‐__b__‐poly(L‐lactide) copolymers (PCL‐__b__‐PLLA) were synthesized via sequential block copolymerization, and their molecular weights and arm length ratio could be accurately controlled. Both differential scanning calorimetr
## Abstract Spirocyclic tin dialkoxides are unique initiators for the ring‐expansion polymerization of lactones leading to complex, but well‐defined macromolecular architectures. In a first example, ε‐caprolactone (εCL) was polymerized, followed by the resumption of polymerization of a mixture of ε