Reversible addition–fragmentation transfer polymerization of p-nitrophenyl acrylate and synthesis of diblock copolymers poly(p-nitrophenyl acrylate)-b-polystyrene

Authors

  • Yong-Chen Hu,

    1. Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China
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  • Ye Liu,

    1. Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China
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  • Cai-Yuan Pan

    Corresponding author
    1. Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China
    • Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China
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Abstract

Poly(p-nitrophenyl acrylate)s (PNPAs) with different molecular mass and narrow polydispersity were successfully synthesized for the first time by reversible addition–fragmentation transfer (RAFT) polymerization with azobisisobutyronitrile (AIBN) as an initiator and [1-(ethoxy carbonyl) prop-1-yl dithiobenzoate] as the chain-transfer agent. Although the molecular mass of PNPAs can be controlled by the molar ratio of NPA to RAFT agent and the conversion, a trace of homo-PNPA was found, especially at the early stage of polymerization. The dithiobenzoyl-terminated PNPA obtained was used as a macro chain-transfer agent in the successive RAFT block copolymerization of styrene (St) with AIBN as the initiator. After purification by two washings with cyclohexane and nitromethane to remove homo-PSt and homo-PNPA, the pure diblock copolymers, PNPA-b-PSt's, with narrow molecular weight distribution were obtained. The structural analysis of polymerization products by 1H NMR and GPC verified the formation of diblock copolymers. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4862–4872, 2004

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