Academic literature on the topic 'Fluorinated silanes'

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Journal articles on the topic "Fluorinated silanes"

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Linnemannstöns, Marvin, Beate Neumann, Hans-Georg Stammler, and Norbert W. Mitzel. "Synthesis and Structural Diversity of Triaryl(phenylethyl)silanes." Synthesis 52, no. 07 (2020): 1025–34. http://dx.doi.org/10.1055/s-0039-1690785.

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Starting from trichloro(phenylethyl)silane, six differently fluorinated triaryl(phenylethyl)silanes were synthesized by salt elimination reactions and their structures were determined by X-ray diffraction analysis. Tris(pentafluorophenyl)(phenylethyl)silane reveals a folded structure due to intramolecular π-stacking interactions, while those with a lower degree of fluorination show either intermolecular π-stacking or no interplay between the aryl groups. A similar folded structure was observed for (4-methylphenethyl)tris(pentafluorophenyl)silane and [2-(naphth-2-yl)ethyl]tris(pentafluorophenyl
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Wang, Hongxia, Jie Ding, Yuhua Xue, Xungai Wang, and Tong Lin. "Superhydrophobic fabrics from hybrid silica sol-gel coatings: Structural effect of precursors on wettability and washing durability." Journal of Materials Research 25, no. 7 (2010): 1336–43. http://dx.doi.org/10.1557/jmr.2010.0169.

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Particle-containing silica sol was synthesized by co-hydrolysis and co-condensation of two silane precursors, tetraethylorthosilicate (TEOS) and an organic silane composed of a non-hydrolyzable functional group (e.g., alkyl, fluorinated alkyl, and phenyl), and used to produce superhydrophobic coatings on fabrics. It has been revealed that the non-hydrolyzable functional groups in the organic silanes have a considerable influence on the fabric surface wettability. When the functional group was long chain alkyl (C16), phenyl, or fluorinated alkyl (C8), the treated surfaces were highly superhydro
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Zemtsov, Artem A., Vitalij V. Levin, Alexander D. Dilman, Marina I. Struchkova, and Vladimir A. Tartakovsky. "Reactions of fluorinated silanes with 2-nitrocinnamates." Journal of Fluorine Chemistry 132, no. 6 (2011): 378–81. http://dx.doi.org/10.1016/j.jfluchem.2011.03.015.

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St. John, Pamela M. "Monolayers of fluorinated silanes as electron-beam resists." Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures 14, no. 1 (1996): 69. http://dx.doi.org/10.1116/1.588436.

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Zemtsov, Artem A., Vitalij V. Levin, Alexander D. Dilman, et al. "Reaction of Baylis-Hillman Adducts with Fluorinated Silanes." European Journal of Organic Chemistry 2010, no. 35 (2010): 6779–85. http://dx.doi.org/10.1002/ejoc.201001051.

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Picard, C., A. Larbot, F. Guida-Pietrasanta, B. Boutevin, and A. Ratsimihety. "Grafting of ceramic membranes by fluorinated silanes: hydrophobic features." Separation and Purification Technology 25, no. 1-3 (2001): 65–69. http://dx.doi.org/10.1016/s1383-5866(01)00091-0.

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Zemtsov, Artem A., Vitalij V. Levin, Alexander D. Dilman, Marina I. Struchkova, and Vladimir A. Tartakovsky. "ChemInform Abstract: Reactions of Fluorinated Silanes with 2-Nitrocinnamates." ChemInform 42, no. 41 (2011): no. http://dx.doi.org/10.1002/chin.201141064.

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Pernisz, U. C., K. G. Sharp, L. Tarhay, and J. J. D'Errico. "Preparation of solar-grade amorphous silicon from fluorinated silanes." Solar Cells 21, no. 1-4 (1987): 195–203. http://dx.doi.org/10.1016/0379-6787(87)90119-0.

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Przybylak, Marcin, Michał Dutkiewicz, Karol Szubert, Hieronim Maciejewski, and Szymon Rojewski. "Multifunctional Cotton Fabrics Obtained by Modification with Silanes Containing Esters of Phosphoric Acid as Substituents." Materials 14, no. 6 (2021): 1542. http://dx.doi.org/10.3390/ma14061542.

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The development of novel flame retardants for cotton textiles that form a stable layer on textile fiber is of high economical and practical relevance. A novel flame retardant fluorinated phosphoric acid esters modified silicone resins for cotton modification were synthesized. The investigated phosphoric acid esters based compounds were substituted by a fluorinated chain or ring, and alkoxysilyl groups. The presence of alkoxysilyl groups allowed the formation of bonds with cellulose, while derivatives of phosphoric esters reduced the flammability of fabrics. Additionally, the presence of fluori
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Chung, Woo Jin, and John T. Welch. "A general method for synthesis of trifluoroacetyltrialkyl(aryl)silanes and the Sakurai reaction of fluorinated acylsilanes with allyl silanes." Journal of Fluorine Chemistry 125, no. 4 (2004): 543–48. http://dx.doi.org/10.1016/j.jfluchem.2003.12.014.

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Dissertations / Theses on the topic "Fluorinated silanes"

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Eklundh, Odler Tea. "Analytical Method Development of Fluorinated Silanes using Mass Spectrometry." Thesis, Örebro universitet, Institutionen för naturvetenskap och teknik, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-71052.

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The aim of this study was to develop an analytical method for fluorinated silanes. Furthermore, as a secondary aim, to explore if there would be possible to detect 1H,1H,2H,2H-perfluorooctyl triethoxysilane (6:2 PTrEtSi) and 1H,1H,2H,2H-perfluorodecyl triethoxysilane (8:2 PTrEtSi) in two different matrices, sludge and cosmetic extract. The method development included experiments using LC-MS, LC-MS/MS, UPC2, GC-MS and APGC-MS/MS and was carried out using standards containing 6:2 PTrEtSi and 8:2 PTrEtSi. The analytical method that worked best for the compounds was GC-MS/MS and an analytical meth
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Tan, Bing. "CONTROLLED SYNTHESIS AND FUNCTIONALIZATION OF NANOPOROUS SOLGEL SILICA PARTICLES AND GELS." UKnowledge, 2005. http://uknowledge.uky.edu/gradschool_diss/305.

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This dissertation addresses three research areas in the sol-gel synthesis of functionalmaterials. The first is the kinetics of hydrolysis and condensation of variousorganoalkoxysilanes. Two mathematical models are developed for the sol-gel reaction inbasic conditions with and without nearest-neighbor effects. Effects on reactivity aremeasured with systematic changes in the organic group structure. Replacing onemethoxy group on the precursor with a methyl group decelerates hydrolysis under basicconditions, but accelerates condensation under acidic conditions. Replacing two methylfunctionalprecu
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Joo, Minjung. "Silane terminated macromonomers with nanoparticles and surface segregation of fluorinated moieties." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1478876813425998.

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Conference papers on the topic "Fluorinated silanes"

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Ok, Jeong Tae, Eugene Lopez-On˜a, Harris Wong, and Sunggook Park. "Effect of Surface Wetting of Micro/Nano Ratchets on Leidenfrost Liquid Drop Motion." In ASME 2009 7th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2009. http://dx.doi.org/10.1115/icnmm2009-82173.

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A micro- and nanoscale asymmetric potential enhances propulsion of liquid drop motion in the Leidenfrost (film boiling) regime. However, the requirement of high operation temperature to levitate a liquid droplet is a critical drawback for practical application of micro- and nanosystems. In this study, we show that the threshold temperature for the droplet motion can be reduced by controlling the wetting properties of ratchet surfaces. Various sizes of metallic ratchets down to sub-micrometer period were fabricated using micro- and nanoscale machining tools. Then, the wettability of the ratchet
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