4.7 Article

How the Reactive End Group of Macro-RAFT Agent Affects RAFT-Mediated Emulsion Polymerization-Induced Self-Assembly

Journal

MACROMOLECULAR RAPID COMMUNICATIONS
Volume 42, Issue 19, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202100333

Keywords

block copolymer nano-objects; polymerization-induced self-assembly; RAFT-mediated emulsion polymerization; reactive end groups

Funding

  1. National Natural Science Foundation of China [21971047]
  2. Innovation Project of Education Department in Guangdong [2018KTSCX053]
  3. Guangdong Special Support Program [2017TX04N371]

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This study explores how the reactive end group of macro-RAFT agent affects RAFT-induced emulsion polymerization for the first time. Different end groups were found to influence the morphologies of block copolymer nano-objects and the polymerization process. The use of asymmetric difunctional macro-RAFT agent allows for functionalization of the nano-objects.
Polymerization-induced self-assembly via reversible addition-fragmentation chain transfer (RAFT)-mediated emulsion polymerization is an emerging method in which macro-RAFT agents are chain extended with hydrophobic monomers in water to form block copolymer nano-objects. However, almost all RAFT-mediated emulsion polymerizations are limited to AB diblock copolymers by using monofunctional macro-RAFT agents with non-reactive end groups. In this study, the first investigation on how the reactive end group of macro-RAFT agent affects RAFT-mediated emulsion polymerization is reported. Three macro-RAFT agents with different end groups are synthesized and employed in RAFT-mediated emulsion polymerization. Effects of end groups on morphologies of block copolymer nano-objects and polymerization process are studied. Block copolymer nano-objects prepared by using an asymmetric difunctional macro-RAFT agent can be functionalized by further chain extension on the surface. It is expected that the current study will not only expand the scope of RAFT-mediated emulsion polymerization, but also provide a novel strategy to prepare functional polymer nanoparticles.

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