Issue 14, 2015

A facile strategy for the synthesis of block copolymers bearing an acid-cleavable junction

Abstract

Post-cleavable block copolymers are crucially important for the fabrication of nanoporous structures from the self-assembly of block copolymers by the selective etching of one block. Here, we present a facile and inexpensive approach to synthesize block copolymers bearing an acid-cleavable junction. A difunctional inifer containing an acetal group is synthesized for the sequential reversible addition–fragmentation transfer (RAFT) polymerization of tert-butyl methacrylate and atom transfer radical polymerization (ATRP) of styrene. Moreover, the polymerization sequence of the monomers can be altered. The acetal junctions in the resulting block copolymers can be readily cleaved by acid under ambient conditions. Aldehyde or monoglyceride end groups are left at the ends of the PS residues, which can be used as binding sites for future applications.

Graphical abstract: A facile strategy for the synthesis of block copolymers bearing an acid-cleavable junction

Article information

Article type
Paper
Submitted
15 Jan 2015
Accepted
16 Feb 2015
First published
17 Feb 2015

Polym. Chem., 2015,6, 2777-2782

Author version available

A facile strategy for the synthesis of block copolymers bearing an acid-cleavable junction

X. Sui, Z. Zhang, S. Guan, Y. Xu, C. Li, Y. Lv, A. Chen, L. Yang and L. Gao, Polym. Chem., 2015, 6, 2777 DOI: 10.1039/C5PY00058K

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