Synthesis of poly[ε-caprolacton-b-epichlorohydryin-b-ε-caprolactone]- g-poly(styrene) Block-Graft Copolymers via Cationic Ring Opening and Atom Transfer Radical Polymerization Transformations
Abstract
The poly[(ε-caprolacton-b-epichlorohydrin-b-ε-caprolactone)]-g-(polystyrene-) [(PCL-b-ECH-bPCL)]-g-PS block-graft copolymers were prepared via cationic, ring opening (ROP) and atom transfer radical
polymerization (ATRP) transformations. With this goal in the frst, cationic ring-opening technique was used to
polymerize the epichlorohydrin (ECH). The ring opening polymerisation (ROP) of ε-caprolactone (ε-CL) was
carried out using poly (epichlorohydrin) (PECH) with hydroxyl functional groups acting as initiators at 110 ºC to
yield poly(ε-caprolacton-b-epichlorohydrin-b-ε-caprolactone) (PCL-PECH-PCL) block copolymer. Finally, in the
atom transfer radical polymerisation (ATRP) of the styrene, chloromethyl groups of the PECH segment of PCLPECH-PCL were used as the starting functional group. [PCL-b-PECH-b-CL] -g-PS graft copolymer block was
obtained as a result of polymerization. The results of the analysis indicated that the molecular weights of the graft
copolymers increased linearly with styrene polymerisation. Synthesized polymers were characterized by 1 H-NMR,
GPC and DSC techniques.
Keywords
References
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Details
Primary Language
English
Subjects
-
Journal Section
Research Article
Publication Date
September 30, 2017
Submission Date
March 28, 2017
Acceptance Date
May 17, 2017
Published in Issue
Year 2017 Volume: 7 Number: 3