4.7 Article

Controlling ring-opening copolymerization of ε-caprolactone with trimethylene carbonate by scandium tris(2,6-di-tert-butyl-4-methylphenolate)

Journal

MACROMOLECULES
Volume 37, Issue 3, Pages 758-763

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma035352f

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Copolymers of epsilon-caprolactone (CL) and trimethylene carbonate (TMC) have been synthesized through ring-opening polymerization using a novel initiator of scandium tris(2,6-di-tert-butyl-4-methylphenolate). CL and TMC polymerizations proceed via the coordination anionic mechanism with acyl-oxygen bond cleavage. Five kinds of copolymers with different structures of X, XB, AXB, AB, and BAY-B are synthesized under different polymerization conditions and characterized by H-1 NMR, GPC, and DSC, where X, A, and B denote as random blocks of CL and TMC, PTMC blocks, and PCL blocks, respectively.

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