Block and star block copolymers by mechanism transformation. II. Synthesis of poly(DOP-b-St) by combination of ATRP and CROP
β Scribed by Yijin Xu; Caiyuan Pan; Lei Tao
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 165 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
Styrene underwent the ATRP process using an asymmetric difunctional initiator, 2-hydroxylethyl 2Π-bromobutyrate in combination with CuBr and 2,2Π-bipyridine (bpy). Polystyrene with hydroxyl and bromine groups at each end of the polymer (HO-PSt-Br) was obtained, and used as a chain-transfer agent in the cationic ringopening polymerization of 1,3-dioxepane with triflic acid as initiator. The structures of the polymerization products were analyzed by 1 H NMR and GPC analyses, indicating the formation of block copolymer. The molecular weight distribution of the block copolymer was relatively narrow and the molecular weight of the polyDOP block was high.
π SIMILAR VOLUMES
Polystyrene (PSt) with end-terminal bromine (Br-PSt-Br) was synthesized by the atom transfer radical polymerization of styrene with the difunctional initiator 1,2-bis(2Π-bromobutyryloxy)ethane in combination with CuBr and bipyridine. The Br-PSt-Br reacted with silver perchlorate at Οͺ78 Β°C, and the r