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A Green Step to New Monomers and Their Polymerization
Author(s) -
Strehmel Veronika,
Strunk David,
Heinz Markus,
Walther Sebastian
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.202002526
Subject(s) - polymerization , radical polymerization , polymer chemistry , monomer , bulk polymerization , chain growth polymerization , methacrylate , acrylate , chemistry , photopolymer , polymer , solution polymerization , reversible addition−fragmentation chain transfer polymerization , ionic polymerization , materials science , organic chemistry
Extract obtained from the bark of Betula Pendula was treated with sodium hydroxide solution to obtain 4‐(4‐hydroxyphenyl)butan‐2‐one. New (meth)acrylates were synthesized on the basis of 4‐(4‐hydroxyphenyl)butan‐2‐one. Free radical polymerization of the new (meth)acrylates was compared with that of commercial monomers (e. g. phenyl(meth)acrylate, 2‐phenoxyethyl methacrylate, and benzyl methacrylate) in solution resulting in soluble polymers as expected in all examples. In contrast to this, free radical polymerization of 4‐(4‐acryloyloxyphenyl)butan‐2‐one in bulk resulted in a crosslinked material although an extremely high molecular weight soluble polymer was received in case of bulk polymerization of 4‐(4‐methacryloyloxyphenyl)butan‐2‐one. The 3‐oxobutyl substituent at the phenyl ring of these monomers may influence their radical polymerization. Furthermore, enzyme mediated radical polymerization and photoinitiated polymerization were applied for the polymer synthesis using 4‐(4‐methacryloyloxyphenyl)butan‐2‐one.