2012
DOI: 10.1134/s0040579512050089
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Synthesizing the components of photopolymerizing acryl composites for production of waveguides with high transparency within telecommunication spectral regions

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Cited by 5 publications
(4 citation statements)
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“…Shashkova et al developed methods to synthesize hydrocarbon and fluorine-containing monomers and oligomers for the creation of planar polymer waveguides. These authors synthesized more than 20 mono- and bifunctional methacrylates of hydrocarbon and fluorinated alcohols, glycols, and diols, and characterized their physicochemical properties.…”
Section: Applicationsmentioning
confidence: 99%
“…Shashkova et al developed methods to synthesize hydrocarbon and fluorine-containing monomers and oligomers for the creation of planar polymer waveguides. These authors synthesized more than 20 mono- and bifunctional methacrylates of hydrocarbon and fluorinated alcohols, glycols, and diols, and characterized their physicochemical properties.…”
Section: Applicationsmentioning
confidence: 99%
“…The use of a solvent (cyclohexane) and a reducing agent was necessary. The synthesis of TMPTA [ 37 ] (and of ditrimethylolpropane acrylate, DTMPA [ 21 ]) has been elaborated using p -toluenesulfonic acid as a catalyst. Nevertheless, the high temperature (140 °C) and the use of benzene or toluene as solvents raise safety concerns regarding the proposed processes.…”
Section: Resultsmentioning
confidence: 99%
“…In alternative studies, 1,3-propanesultone (PS)-functionalized imidazole ionic liquids (ILs) [35] and sulfonated phenylamines [36] are introduced as recyclable acid catalysts, achieving a trimethylolpropane conversion of 100% and TMPTA selectivity of up to 86.4% at 110 • C. The use of a solvent (cyclohexane) and a reducing agent was necessary. The synthesis of TMPTA [37] (and of ditrimethylolpropane acrylate, DTMPA [21]) has been elaborated using p-toluenesulfonic acid as a catalyst. Nevertheless, the high temperature (140 • C) and the use of benzene or toluene as solvents raise safety concerns regarding the proposed processes.…”
Section: Resultsmentioning
confidence: 99%
“…However, to our knowledge, there are no reported detections of FC8-diol, FC10-diol, or FC8-DOD in the environment. Published literature on FC8-diol and FC10-diol pertain mostly to synthetic chemistry research and technical applications such as their ability to form layers and films between water and air or water and hexane, uses in production of various types of nanomaterials, generation of fluorinated multiblock molecules, and others. Patents referencing these compounds suggest their use in the manufacture of dental resins, medical implant components and biotextiles, polyacrylate coatings, oil-repellent sheets, photosensitive resins and adhesives, conductive films, thin metal electrode films, gas sensors, acoustic wave sensors, thermal acid generators, pattern treatment and pattern processing methods, optical polymers, and other types of products (PubChem Depositor-Supplied Patent Identifiers; ). However, current use information is too sparse to provide any reasonable estimates of potential environmental releases or loading.…”
Section: Resultsmentioning
confidence: 99%