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The polyester poly(1,10-decanediol /1, 10-sebacate) (PSD) was synthesized by means of Novozyme 435 catalyzed condensation polymeriza- tion of 1,10-decanediol and 1,10-sebacic acid. Both hydroxyl chain ends of the resulting PSD were modi- fied by esterification with α-bromopropionyl bromide to obtain difunctional macroinitiator, which was sub- sequently used in the ATRP of S t using CuCl/2, 2′- bipyridine (bpy) as the catalyst system to afford the triblock copolymer, polystyrene-block-poly(1,10-dec- anediol/1,10-sebacate)-block-polystyrene (PS t-b-PSD- b-PSt). Molecular weight distribution and structure of the resulting triblock copolymer was confirmed by Waters 410 Gel permeation chromatography (GPC) and measurements of nuclear magnetic resonance (NMR) analysis.
The polyester poly (1,10-decanediol / 1, 10-sebacate) (PSD) was synthesized by means of Novozyme 435 catalyzed condensation polymerization of 1,10-decanediol and 1,10-sebacic acid. Both hydroxyl chain ends of the resulting PSD were modi-fied by esterification with α-bromopropionyl bromide to obtain difunctional macroinitiator, which was sub- sequently used in the ATRP of S t using CuCl / 2, 2’- bipyridine (bpy) as the catalyst system to afford the triblock copolymer, polystyrene-block-poly (1,10-decanel / 1,10-sebacate) -block-polystyrene (PS tb-PSD-b-PSt). Molecular weight distribution and structure of the resulting triblock copolymer was was by Waters 410 Gel permeation chromatography (GPC) and measurements of nuclear magnetic resonance (NMR) analysis.