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
Link To Document :
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