Abstract

Well-controlled anionic polymerization of an initiator-functionalized monomer, p-(2,2′-diphenylethyl)styrene (DPES), was achieved for the first time. The polymerization was performed in a mixed solvent of cyclohexane and tetrahydrofuran (THF) at 40 °C with n-BuLi as initiator. When the volume ratio of cyclohexane to THF was 20, the anionic polymerization of DPES showed living polymerization characteristics, and well-defined block copolymer PDPES-b-PS was successfully synthesized. Furthermore, radical polymerization of methyl methacrylate in the presence of PDPES effectively afforded a graft copolymer composed of a polystyrene backbone and poly(methyl methacrylate) branches. The designation of analogous monomers and polymers was of great significance to synthesize a variety of sophisticated copolymer and functionalize polymer materials.

Highlights

  • Anionic polymerization is the most effective method for synthesizing homopolymers, copolymers, block polymers, and ω-functionalized polymers.[1,2,3,4] Anionic polymerization of styrene (St) is the most ideal living system and enables ready access to a variety of well-defined macromolecular architectures.[3]

  • It was expected that the anionic polymerization of DPES was difficult to control

  • The Mn,gel permeation chromatograph (GPC) of PDPES was close to the Mn,th theoretically calculated based upon the feed ratio of DPES to n-BuLi, indicating that no side reactions occurred during the course of the polymerization in cyclohexane

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Summary

Introduction

Anionic polymerization is the most effective method for synthesizing homopolymers, copolymers, block polymers, and ω-functionalized polymers.[1,2,3,4] Anionic polymerization of styrene (St) is the most ideal living system and enables ready access to a variety of well-defined macromolecular architectures.[3]. The polymerization was performed in a mixed solvent of cyclohexane and tetrahydrofuran (THF) at 40 °C with n-BuLi as initiator. When the volume ratio of cyclohexane to THF was 20, the anionic polymerization of DPES showed living polymerization characteristics, and well-defined block copolymer PDPES-b-PS was successfully synthesized.

Results
Conclusion

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