Academic literature on the topic 'Fluorinated compounds'

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Journal articles on the topic "Fluorinated compounds"

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Timperley, Christopher M., Michael Bird, John F. Broderick, Ian Holden, Ian J. Morton, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 104, no. 2 (2000): 215–23. http://dx.doi.org/10.1016/s0022-1139(00)00248-7.

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Timperley, Christopher M., John F. Broderick, Ian Holden, Ian J. Morton, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 106, no. 1 (2000): 43–52. http://dx.doi.org/10.1016/s0022-1139(00)00284-0.

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Timperley, Christopher M., Ian Holden, Ian J. Morton, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 106, no. 2 (2000): 153–61. http://dx.doi.org/10.1016/s0022-1139(00)00327-4.

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Timperley, Christopher M., David J. Sellers, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 107, no. 1 (2001): 155–58. http://dx.doi.org/10.1016/s0022-1139(00)00394-8.

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Timperley, Christopher M., and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 109, no. 2 (2001): 103–11. http://dx.doi.org/10.1016/s0022-1139(01)00362-1.

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Lowe, K. C., and R. L. Powell. "Fluorinated Bioactive Compounds." Journal of Fluorine Chemistry 109, no. 1 (2001): 1. http://dx.doi.org/10.1016/s0022-1139(01)00371-2.

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Timperley, Christopher M., Robert E. Arbon, Sally A. Saunders, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 113, no. 1 (2002): 65–78. http://dx.doi.org/10.1016/s0022-1139(01)00468-7.

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Timperley, Christopher M., Stephen N. Marriott, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 113, no. 1 (2002): 111–22. http://dx.doi.org/10.1016/s0022-1139(01)00493-6.

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Timperley, Christopher M., Sally A. Saunders, Josef Szpalek, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 119, no. 2 (2003): 161–71. http://dx.doi.org/10.1016/s0022-1139(02)00239-7.

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Timperley, Christopher M., Sue Kirkpatrick, Mark Sandford, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 126, no. 6 (2005): 902–6. http://dx.doi.org/10.1016/j.jfluchem.2005.03.026.

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Dissertations / Theses on the topic "Fluorinated compounds"

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Boldon, Sophie. "Fluorous synthesis of fluorinated compounds." Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540126.

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Parkes, Michael Anthony. "Ionisation studies of chlorinated and fluorinated compounds." Thesis, University of Birmingham, 2007. http://etheses.bham.ac.uk//id/eprint/74/.

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Ionisation processes in gas-phase polyatomic molecules have been studied using threshold photoelectron photoion coincidence and selected ion flow tube techniques for cations and an electron attachment mass spectrometer for anions. Cation formation has been studied for fluoroform (CHF\(_3\)), octafluorocyclobutane (\(c\)-C\(_4\)F\(_8\)), octafluorocyclopentene (\(c\)-C\(_5\)F\(_8\)), monochloroethene (C\(_2\)H\(_3\)Cl), the three isomers of dichloroethene (C\(_2\)H\(_2\)Cl\(_2\)) (i.e. 1,1-dichloroethene, (\(Z\))-1,2-dichloroethene and (\(E\))-1,2-dichloroethene), trichloroethene (C\(_2\)HCl\(_
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Padoan, Gennifer. "Synthesis of fluorinated compounds for biomedical applications." Nice, 2012. http://www.theses.fr/2012NICE4044.

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Une méthodologie rapide et économique pour la préparation des PFEs de formule générale (CF2)m(CH2)2O(CH2)nH, obtenus par réaction des 1H,1,H,2H,2H-perfluoro-1-alcanols avec des 1-bromoalcanes sous conditions basiques est fournie. Cette procédure a fourni des produits très purs avec des rendements de plus de 65%. Ensuite, les propriétés physico-chimiques telles que la densité, l’indice de réfraction, etc. Dans un grand choix de solvants ont été étudiées. Leur comparaison avec des n-alcanes partiellement fluorés ont été évalués afin d’étudier le rôle du rapport m/n et l’influence de la liaison é
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Schaff, Jilla. "Fluorinated esters : synthesis and identification." PDXScholar, 1988. https://pdxscholar.library.pdx.edu/open_access_etds/3921.

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Reactions of different alcohols with 2-hydroxy - 1- trifluoromethyl -1,2,2-trifluoroethanesulfonic acid sultone were studied. Six new esters were prepared: C6F5OC(O)CF(CF3)SO2F, CH3CH2OC(O)CF(CF3)SO2F, CF3CH2OC(O)CF(CF3)SO2F, (CF3)2CHOC(O)CF(CF3)SO2F, CH2=CHCH20C(O)CF(CF3)SO2F, (CH2OC(O)CF(CF3)SO2F)2. Analytical data, infrared, nmr and mass spectra are presented supporting the proposed structures for these new compounds.
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Mojally, Mariam. "DNA binding studies of fluorinated bioactive heterocyclic compounds." Thesis, Loughborough University, 2015. https://dspace.lboro.ac.uk/2134/16732.

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Fluorinated heterocyclic compounds have drug like properties and possess a valuable biological activity due to their rigid chemical structures and the high solubility profile. Novel fluorinated heteroarenes have been synthesised by SNAr reaction of a range of fluorinated arenes including pentafluoropyridine, hexafluorobenzene and pentafluorotoluene to introduce a range of groups specially nitriles, benzimidazole, carbazole and benzimidazole. A number of cyclization reactions have been investigated with the aim of forming polycyclic structures that could act as DNA intercalators. The synthesise
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Mohtasham, Javid. "Fluorinated [beta]-sultones as Precursors to Fluorinated Sulfonic Acids, and New Fluorosulfonyl Containing Monomers/Polymers." PDXScholar, 1989. https://pdxscholar.library.pdx.edu/open_access_etds/1250.

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Sulfur trioxide (SO₃) adds to fluoroolefins of the form RCF=CF₂, (where R = F, SF₅, CF₃, CF₃OCF₂, CF₂=CF(CF₂)₂, CF₃(CF₂)₃O, CF₃O(CF₂)₂OCF₂, or CH₂ClCHClCH₂), yielding the fluorinated [beta]-sultones, RCFCF₂OSO₂. In the case of CF₃(CF₂)₃OCF=CF₂, a reverse addition occurs, giving the sultone, CF₃(CF₂)₃CF₂2OCFCF₂SO₂O. The fluoro [beta]-sultones are capable of undergoing different reactions, such as rearrangement, hydrolysis, esterification, and polymerization. These reactions, will result in the formation of compounds containing the fluorosulfonyl grouping (SO₂F); it is this group that yields the
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Cho, Don Mark. "Partially fluorinated polycyclic aromatic compounds synthesis and supramolecular behavior /." Lexington, Ky. : [University of Kentucky Libraries], 2006. http://lib.uky.edu/ETD/ukychem2007t00544/Cho_thesis.pdf.

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Thesis (M.S.)--University of Kentucky, 2006.<br>Title from document title page (viewed on February 27, 2007). Document formatted into pages; contains: xiv, 69 p. : ill. (some col.). Includes abstract and vita. Includes bibliographical references (p. 64-68).
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Cho, Don Mark. "PARTIALLY FLUORINATED POLYCYCLIC AROMATIC COMPOUNDS: SYNTHESIS AND SUPRAMOLECULAR BEHAVIOR." UKnowledge, 2007. http://uknowledge.uky.edu/gradschool_theses/443.

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The field of organic electronics has received much attention over the last few years, and engineering of organic crystals to grow with pi-electron systems arranged in a face-to-face motif has been shown to be beneficial in electronic devices. The effects of combining aromatic and perfluorinated aromatic derivatives have shown that the intramolecular stacking pattern can be changed from an edge-to-face arrangement to that of a face-to-face motif. Before the work described herein, there were no reported studies of the supramolecular behavior of fused polycyclic aromatic compounds with partial pe
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Odello, Paolo. "Chemistry of some model compounds related to fluorinated polymers." Thesis, Durham University, 1993. http://etheses.dur.ac.uk/5553/.

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The work described in this thesis is concerned with three areas which are the generation of stable carbocations from saturated model compounds related to poly- vinylidenefluoride, the development of synthetic routes to fluoro-organo-phosphazenes with intention of obtaining some potential additives for perfluoropolyether fluids operating at elevated temperatures, and pericyclic reactions involving fluorinated olefins.1. We reported that some remarkable conjugated cations, and di-cations (4a) are obtained by reaction of hydrofluorocarbon precursors (4) with an excess of antimony pentafluoride. C
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Begum, Lovely. "The synthesis of fluorinated analogues of biologically active compounds." Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343327.

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Books on the topic "Fluorinated compounds"

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Petrov, Viacheslav A., ed. Fluorinated Heterocyclic Compounds. John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470528952.

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Kazuaki, Tokuhashi, ed. Lifetimes of fluorinated compounds. Nova Science Publishers, 2008.

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Gakh, Andrei A. Fluorinated heterocycles. Edited by American Chemical Society. Division of Fluorine Chemistry and American Chemical Society Meeting. American Chemical Society, 2009.

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El-Koussa, Z. O. Studies on fluorinated organonitrogen compounds. UMIST, 1993.

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Kissa, Erik. Fluorinated surfactants and repellents. 2nd ed. Marcel Dekker, 2001.

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Grot, Walther. Fluorinated ionomers. Wm Andrew Pub, 2008.

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Adamson, A. J. Studies on fluorinated n-heteroaromatic compounds. UMIST, 1993.

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Fluorinated ionomers. 2nd ed. Elsevier/William Andrew, 2011.

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Fluorinated heterocyclic compounds: Synthesis, chemistry, and applications. Wiley, 2009.

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Andrews, Colan Leslie. The synthesis of some novel fluorinated heterocyclic compounds from fluorinated olefinic precursors. University of Birmingham, 1992.

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Book chapters on the topic "Fluorinated compounds"

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Burton, Donald J., and Long Lu. "Fluorinated Organometallic Compounds." In Organofluorine Chemistry. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/3-540-69197-9_2.

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Hiyama, Tamejiro, and Hisashi Yamamoto. "Organic Reactions with Fluorinated Reagents." In Organofluorine Compounds. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-04164-2_8.

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Langlois, Bernard. "Side-Chain Fluorinated Aromatic Compounds." In Organofluorine Chemistry. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1202-2_10.

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Kemnitz, Erhard, Tomaž Skapin, and John M. Winfield. "Preparation of Fluorinated λ-Alumina." In Efficient Preparations of Fluorine Compounds. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118409466.ch67.

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Fialkov, Yu A., and L. M. Yagupolski. "Aromatic Compounds with Fluorinated Side Chains." In Syntheses of Fluoroorganic Compounds. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70207-5_4.

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Moreira, Irina S., Catarina L. Amorim, Cormac D. Murphy, and Paula M. L. Castro. "Strategies for Biodegradation of Fluorinated Compounds." In Approaches in Bioremediation. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-02369-0_11.

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McCafferty, E. "Corrosion Inhibition by Fluorinated Aliphatic Compounds." In SpringerBriefs in Materials. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15648-4_6.

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Asanov, I. P., P. P. Semyannikov, and V. M. Paasonen. "Study of Fluorinated Graphite Intercalation Compounds." In New Trends in Intercalation Compounds for Energy Storage. Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0389-6_29.

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Moilliet, J. S. "Industrial Routes to Ring-Fluorinated Aromatic Compounds." In Organofluorine Chemistry. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1202-2_9.

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Améduri, B., and B. Boutevin. "Synthesis and applications of fluorinated telechelic monodispersed compounds." In Polymer Synthesis Oxidation Processes. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/3-540-55090-9_5.

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Conference papers on the topic "Fluorinated compounds"

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Parekh, K., and P. B. Aswath. "Synthesis of Fluorinated ZDDP Compounds." In STLE/ASME 2006 International Joint Tribology Conference. ASME, 2006. http://dx.doi.org/10.1115/ijtc2006-12053.

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Pausch, Axel E., Thomas Geelhaar, Eike Poetsch, and Ulrich Finkenzeller. "New fluorinated heterocyclic compounds for improved FLC mixtures." In SPIE/IS&T 1992 Symposium on Electronic Imaging: Science and Technology, edited by Paul S. Drzaic and Uzi Efron. SPIE, 1992. http://dx.doi.org/10.1117/12.60381.

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Biliavska, Liubov, Yulia Pankivska, Olga Povnitsa, et al. "Antiviral Activity of Fluorinated Heterocyclic Compounds." In 2nd International Electronic Conference on Medicinal Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecmc-2-a019.

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Tabolin, Andrey, Vladimir Motornov, Valentine Nenajdenko та Sema Ioffeа. "α-FLUORONITROALKENES IN THE SYNTHESIS OF FLUORINATED HETEROCYCLES". У Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m735.aks-2019/123-125.

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Yamashita, Tsuneo, Hisashi Mitsuhashi, and Masamichi Morita. "Novel fluorinated compounds for releasing material in nanoimprint lithography." In SPIE Advanced Lithography, edited by William M. Tong and Douglas J. Resnick. SPIE, 2013. http://dx.doi.org/10.1117/12.2011966.

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Hudson, Bruce S., Mary S. C. Foley, John P. Chan, and M. Z. Zgierski. "Resonance Raman studies of simple fluorinated compounds: trifluoromethyliodide and hexafluorobutadiene." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by John W. Hepburn. SPIE, 1995. http://dx.doi.org/10.1117/12.220854.

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Naumenko, Krystyna, Anna Golovan, Galina Baranova, Svitlana Zagorodnya, and Yurii Shermolovych. "Antiviral and Apoptosis Modulating Potential of Fluorinated Compounds." In 2nd International Electronic Conference on Medicinal Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecmc-2-a029.

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Naumenko, Krystyna, Polina Zaremba, Svitlana Zagorodnya, and Yurii Shermolovych. "Antiviral activity of fluorinated compounds against DNA- and RNA-containing viruses." In 5th International Electronic Conference on Medicinal Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06353.

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Ribeiro, Sandra S., Tamara F. Guimarães, and André L. M. Porto. "Chemoenzymatic resolution of fluorinated compounds by lipase CALB under microwave irradiation." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20131014133533.

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Melandri, Sonia, Laura Favero, Camilla Calabrese, et al. "TUNING OF NON-COVALENT INTERACTIONS IN MOLECULAR COMPLEXES OF FLUORINATED AROMATIC COMPOUNDS." In 73rd International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.wk08.

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Reports on the topic "Fluorinated compounds"

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Waisner, Scott, Victor Medina, Charles Ellison, et al. Design, construction, and testing of the PFAS Effluent Treatment System (PETS), a mobile ion exchange–based system for the treatment of per-, poly-fluorinated alkyl substances (PFAS) contaminated water. Engineer Research and Development Center (U.S.), 2022. http://dx.doi.org/10.21079/11681/43823.

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Poly-,Per-fluorinated alkyl substances (PFAS) are versatile chemicals that were incorporated in a wide range of products. One of their most important use was in aqueous film-forming foams for fighting liquid fuel fires. PFAS compounds have recently been identified as potential environmental contaminants. In the United States there are hundreds of potential military sites with PFAS contamination. The ERDC designed and constructed a mobile treatment system to address small sites (250,000 gallons or less) and as a platform to field test new adsorptive media. The PFAS Effluent Treatment System (PE
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