369371-42-6Relevant articles and documents
Process for preparing fluorohalogenethers
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Page 5, (2008/06/13)
A process for preparing (per)fluorohalogenethers having general formula (II): R′CF2OCFA-CA′F2 ??(II) wherein:— A and A′, equal to or different from each other, are H, Cl or Br but they cannot be both H; R′ has the following meanings: RO—, wherein R is a (per)fluorinated substituent, selected from the following groups: linear or branched C1-C20 alkyl; C3-C7 cycloalkyl; aromatic, C6-C10 arylalkyl or alkylaryl; C5-C10 heterocyclic or alkylheterocyclic; or a perfluoropolyether substituent T—Rf— wherein T=—OCF2OCFA-CA′F2, —OCF2XI, wherein XI=F, CF3, Cl; Rf is a perfluorooxyalkylene chain; by reaction of carbonyl compounds having formula R″COF (III) wherein R″=RO—, or R″=Q-Rf— wherein Q=—OCOF, —OCF2XI; in liquid phase with elemental fluorine and with olefinic compounds having formula CAF=CA′F (IV), at temperatures from ?120° C. to ?20° C.
Fluorovinyl ethers and polymers obtainable therefrom
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, (2008/06/13)
Fluorovinyl ethers having the formula CFX═CXOCF2OR, wherein R is a C2-C6 linear, branched or C5-C6 cyclic (per)fluoroalkyl group, or a C2-C6, linear, branched (per)fluoro oxyalkyl group containing from one to three oxygen atoms; when R is fluoroalkyl or fluorooxyalkyl group as above defined, it can contain from 1 to 2 atoms, equal or different, selected from the following: H, Cl, Br, I; X═F, H; and homopolymers or polymers obtainable polymerizing said Fluorovinyl ethers with at least another polymerizable monomer.