Title of article
Perfluoroalkylated diblock-alkyl methacrylate monomers for biomedical applications: Wettability of their copolymers with HEMA and DEGMA
Author/Authors
Kapl?nek، نويسنده , , Robert and Paleta، نويسنده , , Old?ich and Mich?lek، نويسنده , , Ji?? and P??dn?، نويسنده , , Martin، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
6
From page
593
To page
598
Abstract
The intermediate perfluoroalkylated diblock hydrophobic–hydrophilic secondary alcohols (9–11), which were prepared by the reaction of monomethyl ethers of oligomeric ethyleneglycols with 2-[(perfluoroalkyl)methyl]oxiranes (7 and 8), resulted in the formation of the title monomers (12–14) by the acylation with methacryloyl chloride. Copolymers of 12–14 with HEMA and DEGMA prepared under radical conditions display enhanced swelling properties.
Keywords
Perfluoroalkylated oligoethers , Perfluoroalkylated methacrylates , Double-tail methacrylates , Wettability of methacrylate copolymers , Epoxide ring opening
Journal title
Journal of Fluorine Chemistry
Serial Year
2005
Journal title
Journal of Fluorine Chemistry
Record number
1608891
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