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Biased Lewis Pairs: A General Catalytic Approach to Ether-Ester Block Copolymers with Unlimited Ordering of Sequences.
Liu, Shan; Bai, Tianwen; Ni, Kang; Chen, Ye; Zhao, Junpeng; Ling, Jun; Ye, Xiaodong; Zhang, Guangzhao.
Afiliação
  • Liu S; Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou, 510640, P. R. China.
  • Bai T; MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
  • Ni K; Hefei National Laboratory for Physical Sciences at the Microscale, Department of Chemical Physics, University of Science and Technology of China, Hefei, 230026, China.
  • Chen Y; Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou, 510640, P. R. China.
  • Zhao J; Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou, 510640, P. R. China.
  • Ling J; MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
  • Ye X; Hefei National Laboratory for Physical Sciences at the Microscale, Department of Chemical Physics, University of Science and Technology of China, Hefei, 230026, China.
  • Zhang G; Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou, 510640, P. R. China.
Angew Chem Int Ed Engl ; 58(43): 15478-15487, 2019 Oct 21.
Article em En | MEDLINE | ID: mdl-31464086
ABSTRACT
Polymerizing epoxides after cyclic esters remains a major challenge, though their block copolymers have been extensively studied and used for decades. Reported here is a simple catalytic approach based on a metal-free Lewis pair that addresses the challenge. When the Lewis acid is used in excess of a base, selective (transesterification-free) polymerization of epoxides occurs in the presence of esters, while selectivity toward cyclic esters is achieved by an oppositely biased catalyst. Hence, one-pot block copolymerization can be performed in both ester-first and ether-first orders with selectivity being switchable at any stage, yielding ether-ester-type block copolymers with unlimited ordering of sequences as well as widely variable compositions and architectures. The selectivity can also be switched back and forth several times to generate a multiblock copolymer. Experimental and calculational results indicate that the selectivity originates mainly from the state of catalyst-activated hydroxy species.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2019 Tipo de documento: Article