1955
DOI: 10.1002/pol.1955.120158018
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Fluorine‐containing polymers. II. 1, 1‐dihydroperfluoroalkyl acrylates: Preparation of monomers1

Abstract: Acrylate esters of seven n‐1,1‐dihydroperfluoroalkanols have been synthesized. The esters are: 1,1‐dihydroperfluoroethyl‐; 1,1‐dihydroperfluoropropyl‐; 1,1‐dihydroperfluorobutyl‐; 1,1‐dihydroperfluoropentyl‐; 1,1‐dihydroperfluorohexyl‐; 1,1‐dihydroperfluorooctyl‐; and 1,1‐dihydroperfluorodecyl acrylates. Since these alcohols were difficult to esterify using conventional procedures, acrylyl chloride or acrylic acid plus perfluoroacetic anhydride have been empolyed in this work.

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Cited by 31 publications
(12 citation statements)
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“…Startdispersity of the colloids were determined by dynamic light ing from these monomers, we tried to synthesize highly scattering. A plot of the particle diameter as a function of charged polymer colloids (6).…”
Section: Resultsmentioning
confidence: 99%
“…Startdispersity of the colloids were determined by dynamic light ing from these monomers, we tried to synthesize highly scattering. A plot of the particle diameter as a function of charged polymer colloids (6).…”
Section: Resultsmentioning
confidence: 99%
“…16 The details of the emulsion polymerization will be presented elsewhere. 17 After purification by diafiltration the size of the polymer colloids was determined with dynamic light scattering. A mean diameter of 500 nm and an refractive index n D 20 ϭ1.37 was obtained.…”
Section: Methodsmentioning
confidence: 99%
“…Fresh distillation and adsorption of stabilizer on silica gel usually precede polymerization. A survey of the most common monomers is shown in the following equations; their physical constants are given in Table 31 [234][235][236][237][238][239][240][241][242]. The polymerization of fluorinated monomers, particularly chlorotrifluoroethylene and tetrafluoroethylene, in chloroform solutions using high concentrations (up to 5 %) of dibenzoyl peroxide gives low-molecularweight oils and greases which are used as inert liquids and lubricants [243].…”
Section: Monomersmentioning
confidence: 99%
“…Under special conditions, addition products can be isolated (408). (240) C4HgSH, Triton B l44 0 C. 7 days, 65°C, 0.5 hr CF=CF 1 1 CF2-CFa [408] C4HgSCH-CFSC4 H 9 1 1 CF2-CF2 30%…”
Section: Alkylations At Sulfurmentioning
confidence: 99%
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