Answers are grounded in this paper and cite their sources.
A series of fluorinated acrylates [F(CF 2 ) q (CH 2 ) p OCOCHCH 2 , where q = 8 and p = 2 ÷ 11) were synthesized and used as comonomers in the photopolymerization of acrylic systems. These fluoroacrylates were synthesized in a three‐step procedure through the radical addition of perfluoroalkyliodides to an unsaturated alcohol followed by their acrylation. The mixtures, containing up to 0.8% (w/w) of the comonomers, produced transparent films after UV curing; they showed changes in the surface properties as a function of the comonomer type and concentration. With contact‐angle and X‐ray photoelectron spectroscopy analyses, the relationship between the structure of the monomers and the surface properties of the UV‐cured films was investigated: the wettability decreased, depending on the length of the fluorinated group ( q value) and the hydrogenated segment of the monomer ( p value).
No takes yet. Share an insight, caveat, or question.
Améduri et al. (2001) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: