Tailored hydrolytically stable polyacid gels based on curable poly(acrylic acid)s and bisacrylamides

Poly(acrylic acid)s (PAAs) with curable methacrylamide moieties as well as bisacrylamide crosslinkers are described as components for well‐defined hydrogels with increased hydrolytic resistance. PAAs with tethered curing moieties of different alkyl spacer lengths (−(CH2)n−, n = 2, 3, 6 or 8) were pr...

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Published inPolymer international Vol. 65; no. 10; pp. 1142 - 1149
Main Authors Lampe, Ulrich, Maier, Maximilian, Klee, Joachim E, Ritter, Helmut
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.10.2016
Wiley Subscription Services, Inc
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Summary:Poly(acrylic acid)s (PAAs) with curable methacrylamide moieties as well as bisacrylamide crosslinkers are described as components for well‐defined hydrogels with increased hydrolytic resistance. PAAs with tethered curing moieties of different alkyl spacer lengths (−(CH2)n−, n = 2, 3, 6 or 8) were prepared via copolymerization of one‐sided methacrylated diamines with protected acrylic acid, followed by polymer‐analogous methacrylation and deprotection. Bisacrylamide crosslinkers were synthesized by acrylation of diamines with different cores and N‐substitutes like allyl, cyclopropyl or propyl groups. Both components were subsequently combined for the formation of novel amide based hydrogels. Network densities of the obtained gels were elucidated by rheokinetic investigations. © 2016 Society of Chemical Industry Hydrolytically stable hydrogels were obtained by crosslinking of novel poly(acrylic acid) copolymers, modified with curable moieties and different side‐chain spacer lengths and bisacrylamide crosslinkers. Network strength was determined by rheokinetic investigations.
Bibliography:ark:/67375/WNG-7X6RHFNS-Q
ArticleID:PI5179
Figure S1. 1H-NMR-spectra (300 MHz, D2O) of monomethacrylated diamines 1a-d. Figure S2. Exemplary 1H-NMR-spectra (300 MHz, DMSO-d6) of methacrylated, hydrolyzed polyacids 3a and 3d.
istex:77528B3003D50CC5ED65C5A999AF7B16437FA3B6
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0959-8103
1097-0126
DOI:10.1002/pi.5179