## Abstract **Summary:** Bis(hydroxy)telechelic bisphenol A polycarbonate (PC) was prepared via melt polycondensation of bisphenol A (BPA) and diphenyl carbonate (DPC) using lanthanum(III) acetylacetonate as a catalyst for transesterification. Subsequently, the polycarbonate was converted to a bifu
Synthesis and Characterization of Poly(trimethylene oxide)-block-Polystyrene and Poly(trimethylene oxide)-block-Polystyrene-block-Poly(methyl methacrylate) by Combination of Atom Transfer Radical Polymerization (ATRP) and Cationic Ring-Opening Polymerization (CROP)
✍ Scribed by Bin Luan; Qin Yuan; Cai-Yuan Pan
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 159 KB
- Volume
- 205
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Summary: Diblock copolymers, poly(trimethylene oxide)‐block‐poly(styrene)s abbreviated as poly(TMO)‐block‐poly(St), and triblock copolymers, poly(TMO)‐block‐poly(St)‐block‐poly(MMA)s (MMA = methyl methacrylate), with controlled molecular weight and narrow polydispersity have been successively synthesized by a combination of atom transfer radical polymerization (ATRP) and cationic ring‐opening polymerization using the bifunctional initiator, 2‐hydroxylethyl α‐bromoisobutyrate, without intermediate function transformation. The gel permeation chromatography (GPC) and NMR analyses confirmed the structures of di‐ and triblock copolymers obtained.
GPC curves of (a) poly(St); (b) diblock copolymer, poly(St)‐block‐poly(MMA) before precipitation; (c) poly(St)‐block‐poly(MMA) after precipitation in cyclohexane/ethanol (2:1); (d) triblock copolymer, poly(TMO)‐block‐poly(St)‐block‐poly(MMA).
magnified imageGPC curves of (a) poly(St); (b) diblock copolymer, poly(St)‐block‐poly(MMA) before precipitation; (c) poly(St)‐block‐poly(MMA) after precipitation in cyclohexane/ethanol (2:1); (d) triblock copolymer, poly(TMO)‐block‐poly(St)‐block‐poly(MMA).
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