Kinetic comparison of isomeric oligo(ethylene oxide) (meth)acrylates: Aqueous polymerization of oligo(ethylene oxide) methyl ether methacrylate and methyl 2‐(oligo(ethylene oxide) methyl ether)acrylate macromonomers
Kinetic comparison of isomeric oligo(ethylene oxide) (meth)acrylates: Aqueous polymerization of oligo(ethylene oxide) methyl ether methacrylate and methyl 2‐(oligo(ethylene oxide) methyl ether)acrylate macromonomers
复制标题
DOI:
10.1002/pol.20220086
复制
发表时间:
2022-04
影响因子:
3.4
通讯作者:
Michael R. Martinez;Sylwia Dworakowska;Adam Gorczyński;Grzegorz Szczepaniak;Ferdinando de Luca Bossa;K. Matyjaszewski
中科院分区:
文献类型:
--
作者:
Michael R. Martinez;Sylwia Dworakowska;Adam Gorczyński;Grzegorz Szczepaniak;Ferdinando de Luca Bossa;K. Matyjaszewski
The photoinduced energy/electron transfer‐reversible addition‐fragmentation chain transfer (PET‐RAFT) polymerizations of oligo(ethylene oxide) monomethyl ether methacrylate (OEOMA, also known as poly[ethylene glycol] methyl ether methacrylate, PEGMA) and isomeric methyl 2‐(oligo(ethylene oxide) methyl ether)acrylate (2OEOAM) macromonomers with OEO average degree of polymerization of 22 or 45 were conducted in aqueous media to provide insight into the effect of monomer structure on grafting‐through RAFT of 1,1‐disubstituted acrylic macromonomers. The polymerizations of all four monomers reached nearly quantitative conversion. The longer macromonomers polymerized faster than the shorter ones within the same monomer class. The OEO side chain at the α (i.e., 2‐) position of isomeric acrylates significantly slowed RAFT polymerization in comparison with OEO ester side chain of methacrylates.