Relevant bibliographies by topics / Sulfonic acids

Academic literature on the topic 'Sulfonic acids'

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Published: 4 June 2021
Last updated: 3 March 2023

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Journal articles on the topic "Sulfonic acids"

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Lezina, Olga M., Svetlana N. Subbotina, Larisa L. Frolova, Svetlana A. Rubtsova, and Denis V. Sudarikov. "Synthesis and Oxidative Transformations of New Chiral Pinane-Type γ-Ketothiols: Stereochemical Features of Reactions." Molecules 26, no. 17 (August 29, 2021): 5245. http://dx.doi.org/10.3390/molecules26175245.

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Chiral γ-ketothiols, thioacetates, thiobenzoate, disulfides, sulfones, thiosulfonates, and sulfonic acids were obtained from β-pinene for the first time. New compounds open up prospects for the synthesis of other polyfunctional compounds combining a biologically active pinane fragment with various pharmacophore groups. It was shown that the syntheses of sulfanyl and sulfonyl derivatives based on 2-norpinanone are characterized by high stereoselectivity in comparison with similar reactions of pinocarvone. The conditions for the preparation of diastereomerically pure thioacetyl and thiobenzoyl derivatives based on pinocarvone, as well as for the chemoselective oxidation of γ-ketothiols with chlorine dioxide to the corresponding thiolsulfonates and sulfonic acids, were selected. The effect of the VO(acac)2 catalyst on the increase in the yields of thiosulfonates was shown. A new direction of the transformation of thiosulfonates with the formation of sulfones was revealed. In the case of pinocarvone-based sulfones, the configuration is inversed at the C2 atom. An epimerization scheme is proposed.
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Kiani, Adeleh, Batool Akhlaghinia, Hamed Rouhi-Saadabad, and Mehdi Bakavoli. "Direct synthesis of sulfonyl azides from sulfonic acids." Journal of Sulfur Chemistry 35, no. 2 (June 4, 2013): 119–27. http://dx.doi.org/10.1080/17415993.2013.801476.

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Jiang, Ying, Njud S. Alharbi, Bing Sun, and Hua-Li Qin. "Facile one-pot synthesis of sulfonyl fluorides from sulfonates or sulfonic acids." RSC Advances 9, no. 24 (2019): 13863–67. http://dx.doi.org/10.1039/c9ra02531f.

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Bahrami, Kiumars. "TAPC-Promoted Synthesis of Sulfonyl Chlorides from Sulfonic Acids." Synlett 2011, no. 18 (October 19, 2011): 2671–74. http://dx.doi.org/10.1055/s-0031-1289547.

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Su, Debao, Wenbiao Cen, Robert L. Kirchmeier, and Jean'ne M. Shreeve. "Synthesis of fluorinated phosphonic, sulfonic, and mixed phosphonic/sulfonic acids." Canadian Journal of Chemistry 67, no. 11 (November 1, 1989): 1795–99. http://dx.doi.org/10.1139/v89-278.

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The acids (HO)2P(O)CFHSO3H, (HO)2P(O)(CF2)4O(CF2)2SO3H, H(CF2)2O(CF2)2P(O)(OH)2, H(CF2)2O(CF2)4P(O)(OH)2, (HO)2P(O)(CF2)2O(CF2)4H, and the acid precursor (C2H5O)2P(O)CF(SO3Na)2 have been synthesized. Elemental analysis, 19F, 1H, and 31P NMR, and mass spectroscopy were used for characterization of these materials. They are very strong acids, and exhibit a high degree of stability in aqueous solution at elevated temperature, which makes them attractive candidates for use as electrolytes in fuel cells. Keywords: fluorinated phosphonic acids; fluorinated sulfonic acids; 1H, 19F, 31P NMR.
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Peng, Zhen, Yun-Yun Hong, Sha Peng, Xiang-Qun Xu, Shan-Shan Tang, Li-Hua Yang, and Long-Yong Xie. "Photosensitizer-free synthesis of β-keto sulfones via visible-light-induced oxysulfonylation of alkenes with sulfonic acids." Organic & Biomolecular Chemistry 19, no. 20 (2021): 4537–41. http://dx.doi.org/10.1039/d1ob00552a.

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A practical and environment-friendly methodology for the construction of β-keto sulfones through visible-light induced direct oxysulfonylation of alkenes with sulfonic acids under open-air and photosensitizer-free conditions was developed.
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Badali, Elham, Hossein Rahimzadeh, Ali Sharifi, Azizollah Habibi, and Azim Ziyaei Halimehjani. "Nitroepoxide ring opening with thionucleophiles in water: synthesis of α-xanthyl ketones, β-keto sulfones and β-keto sulfonic acids." Organic & Biomolecular Chemistry 18, no. 26 (2020): 4983–87. http://dx.doi.org/10.1039/d0ob00941e.

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Nitroepoxide ring opening with thionucleophiles such as potassium xanthates, sodium aryl sulfinates and sodium bisulfite in water is investigated to provide the corresponding α-xanthyl-α-aryl-2-propanones, β-keto sulfones and β-keto sulfonic acids.
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Jang, Doo, and Joong-Gon Kim. "Convenient One-Pot Synthesis of Sulfonyl Azides from Sulfonic Acids." Synlett 2008, no. 18 (October 23, 2008): 2885–87. http://dx.doi.org/10.1055/s-0028-1083600.

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Bahrami, Kiumars, Mohammad Khodaei, and Jamshid Abbasi. "Synthesis of Sulfonyl Chlorides and Sulfonic Acids in SDS Micelles." Synthesis 2012, no. 02 (November 30, 2011): 316–22. http://dx.doi.org/10.1055/s-0031-1289628.

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Chuev, V. G., A. F. Evleev, A. F. Ermolov, M. A. Kurykin, S. V. Povroznik, and G. A. Sokol'sky. "New fluorine-containing sulfonic acids." Journal of Fluorine Chemistry 58, no. 2-3 (August 1992): 359. http://dx.doi.org/10.1016/s0022-1139(00)80824-6.

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Dissertations / Theses on the topic "Sulfonic acids"

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Terjeson, Robin Joyce. "The Chemistry of Sulfonyl Fluorides: SF5 and/or SO2F Containing Compounds as Precursors to Sulfonic Acids." PDXScholar, 1989. https://pdxscholar.library.pdx.edu/open_access_etds/1241.

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Sulfonyl fluoride systems and their derivatives, RS02F, where R represents hydrocarbon/fluorocarbon moieties continue to be of considerable interest. The incorporation of the sulfonyl fluoride group (S02F) into molecular systems can lead to compounds that are useful as ion-exchange resins, surface active agents, fuel cell electrolytes, and strong sulfonic acids/salts. Interest in preparing SF5 containing sulfonyl fluorides led to the synthesis of the ᵝ-sultone, SF5CHCF20S02, and its rearranged product. Hydrolysis of the sultone gave SF5CH2S02F which led to the sulfonic acid and salt, SF5CH2S03H•H20 and (SF5CH2S03)2Ca. Esters of the sultone were prepared by reaction of the sultone with fluorinated alcohols in the presence of NaF to give SF5CH(S02F)C(O)OR where R = CH2CF3 and CH(CF3)2. Polymeric SF5/S02F containing esters were prepared by reaction of allyl esters, RCX(S02F)C(O)OCH2CH=CH2, in ultraviolet light where R = CF3 or SF5 and X= H or F. Fluorinated silver carboxylate salts have been useful in preparing fluoroesters from alkyl iodides. Therefore, a new silver salt, FS02CF2C(0)0Ag was prepared and characterized; its reaction with (CH3)3SiI, HOCH2CH2I and alkyl bromides and iodides are reported. In addition, new SF5 containing fluoropolymers were synthesized via reaction of fluorinated olefins with SF5Br. Reactions of SF5 containing olefins with CF30Cl, C1F and Cl2 provide reagents that may be of potential use as precursors to sulfonyl fluoride containing systems. All new compounds were characterized by their respective infrared, nmr and mass spectra.
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Hamel, Nicolas Noel. "Monomeric and Polymeric Fluoroalkyl Sulfonyl Fluorides, Sulfonate Salts and Sulfonic Acids for Use as Electrolytes and Coatings." PDXScholar, 1995. https://pdxscholar.library.pdx.edu/open_access_etds/1265.

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Monomeric and polymeric fluoroalkyl sulfonyl fluorides, sulfonate salts and sulfonic acids have qualities desirable for use as electrolytes in alternative energy sources such as fuel cells and solid polymer electrolyte lithium batteries. Since the nature of the fluoroalkyl group affects the properties of these compounds, new monomeric and polymeric fluoroalkyl sulfonyl fluorides, sulfonate salts and sulfonic acids were prepared in this work. Simple compounds prepared in this work were: the fluoroalkyl sulfonyl fluorides, sulfonate salts and sulfonic acid CHF (OCF₂CF2SO₂ F)₂ CF₂(OCF₂CF₂SO₂F) ₂ CH₂(OCF₂CF₂SO3Na) ₂ CF₂(OCF₂CF₂SO3 ) ₂Ca , CF₂(OCF₂CF₂SO3H) ₂ prepared by means of electrochemical fluorination; FC (CF3 ) ₂OCH₂CH₂OCF₂CF₂SO₂F prepared using the adduct of hexafluoroacetone and silver fluoride; CH₃OCF₂CF₂SO₂F prepared as a substrate for free-radical substitution reactions of fluorinated species; and the pentafluorosulfur lithium sulfonate salts SFsCHFSO₃Li and SFsCF₂SO₃Li. Novel compounds containing both alcohol and fluoroalkyl sulfonyl functional groups were prepared: the chlorohydrin ClCH₂CH (OH) CH₂OCF₂CF₂SO₂F; the benzyl ethers HOCH₂CH (OCH₂C6Hs) CH₂OCF₂CF₂SO₂F and C6HsCH₂OCH₂CH (OH) CH₂OCF₂CF₂SO₂F as a product mixture; and the diol HOCH₂CH (OH) CH₂OCF₂CF₂SO₂F. The diol was found to be a useful synthon for the preparation of two polymeric fluoroalkyl sulfonyl fluorides: the polyester [C (O)CF₂CF₂CF₂ C (O) OCH₂CH (CH₂OCF₂) CF₂SO₂F] O]n by reaction with perfluoroglutaric anhydride and a polyurethane formed with 1,6-diisocyanohexane. Other polymeric compounds prepared were: the sulfonyl fluoride, sulfonate salt and sulfonic acid [OCH₂CH (CH₂OCF₂CF₂SO₂F)]n, [OCH₂CH (CH₂OCF₂CF₂SO₃Na)]n, and [OCH₂CH (CH₂OCF₂CF₂SO₃H)]n prepared by homopolymerization of the epoxide OCH₂CHCH₂OCF₂CF₂SO₂F; a cross-linked copolymer of the same epoxide; and the fluoroalkyl sulfonyl fluoride polyacrylat [-CH₂-CH-(CO₂CH₂CH₂CF₂CF₂OCF₂CF₂SO₂F)]n prepared from the acrylate ester H₂C=CHC (O) OCH₂CH₂CF₂SO₂F. ¹H, ¹⁹F and ¹³C nuclear magnetic resonance spectroscopy, infrared spectroscopy, mass spectrometry, melting point or boiling point, elemental analysis, contact angles, optical clarity, refractive index, and specific conductivity were among the techniques used to characterize the compounds.
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Rambocus, Subhas. "Reactive solvent extraction of dicarboxylic and carboxylic-sulfonic acids." Thesis, London South Bank University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.245144.

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Willenbring, Robert J. "Synthesis and characterization of some SF₅- containing sulfonic acids." PDXScholar, 1987. https://pdxscholar.library.pdx.edu/open_access_etds/3734.

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Pentafluorosulfur (VI) bromide (SF5Br) adds to olefins of the form CX2=CX2, where X= H or F, with the pentafluorosulfur group usually adding to the carbon with more hydrogens attached to it. This series of compounds was used in an attempt to prepare the corresponding sulfonic acid hydrates of the general formula SF5CX2CX2SO3H·nH2O, in order to have these compounds tested as possible fuel cell electrolytes. The reaction scheme involved reflux of the SF5Br adduct with an equimolar amount of sodium sulfite in 50% ethanol for two days, followed by acidification of the recovered solid material using HCl or H2SO4.
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Dong, Daxuan. "Polyphenylene Sulfonic Acids As Proton Exchange Membranes For Fuel Cells." Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1332355539.

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Kusoglu, Ahmet. "Mechanical characterization of perfluorosulfonic acid (PFSA) ionomer membranes." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 203 p, 2009. http://proquest.umi.com/pqdweb?did=1885675131&sid=3&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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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 corresponding sulfonic acid upon base/acid treatment. The addition of sodium bisulfite to CF₃CF= CF₂ and CF₃(CF₂)₄CF=CF₂ in the presence of (C₆H₅CO)₂O₂ and Na₂B₄O₇·10H₂O was also studied to produce the corresponding sulfonic acid hydrates of the general formula, R[subscript f]CFHCF₂SO₃H·nH₂O. These acids were prepared, and thus, tested as possible fuel cell electrolytes. Infrared, ¹H and ¹⁹F nuclear magnetic resonance and mass spectra, as well as elemental analyses, will be presented in order to support the proposed structures for the resulted compounds.
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Winter, Rolf Walter. "Chemistry of Pentafluorothio (SF5) Alkyl Derivatives." PDXScholar, 1990. https://pdxscholar.library.pdx.edu/open_access_etds/1281.

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Part I describes the preparation of a number of useful intermediates from the sultone F5SCHCF2OSO2 (1). These intermediates include the following: the ketene F5SC(SO2)=C=O (21), the unique sultone F4S=CCF2OSO2 (23), and various ionic intermediates of the form Y+ [F5SC(SO2F) COX]-. These intermediates play an important role in providing new pathways for preparing fluorosulfonic acid precursors. Fluorosulfonic acids are excellent candidates to improve the efficiency of environmentally safe fuel cells. It was possible to obtain new derivatives of 1 by various reactions of 21, 23 and the ionic intermediates, but it was not possible to introduce an alkyl substituent with either of the intermediates. Part II is concerned with the synthesis of SF5 containing epoxides as possible monomers. When polymerized, materials of high dielectric strength and high chemical resistance should be obtained. The reaction chemistry of one of the epoxides was investigated and it was found that all reactions studied were accompanied by the loss of the SF5 group. Thus, it was not possible to obtain any polymeric materials. Part III deals with the synthetic accessibility of SF$\sb5$ malonic esters and thence of SF$\sb5$ acrylic esters. These compounds should serve as building blocks in the synthesis of SF$\sb5$ containing pyrimidines. The CF3 analogue, 5-trifluoromethyl uracil, is used as an antiviral drug. In order to synthesize either SF5 malonic ester or 2-SF5 acrylic ester an SF5 group has to be introduced at a secondary carbon. A secondary SF$\sb5$ compound could be synthesized (F5SCH (COOC2H5) (CHBrOAc)) but could not be converted to the respective malonic ester F5SCH (COOC2H5) compound. Part IV describes the reactions and preparations of Parts I-III.
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Hicks, Jason Christopher. "Organic/inorganic hybrid amine and sulfonic acid tethered silica materials synthesis, characterization and application /." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/26583.

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Thesis (Ph.D)--Chemical Engineering, Georgia Institute of Technology, 2008.
Committee Chair: Jones, Christopher; Committee Member: Koros, William; Committee Member: Lyon, Andrew; Committee Member: Nair, Sankar; Committee Member: Weck, Marcus. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Granados-Focil, Sergio. "A new class of polyelectrolytes, poly(phenylene sulfonic acids) and its copolymers as proton exchange membranes for PEMFC'S." online version, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1129082182.

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Books on the topic "Sulfonic acids"

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Saul, Patai, and Rappoport Zvi, eds. The Chemistry of sulphonic acids, esters, and their derivatives. Chichester [England]: Wiley, 1991.

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W, Cooper George, and United States. National Aeronautics and Space Administration., eds. Sulfur and hydrogen isotope anomalies in meteorite sulfonic acids. [Washington, DC: National Aeronautics and Space Administration, 1997.

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Royal Society of Chemistry (Great Britain), ed. Chlorosulfonic acid: A versatile reagent. Cambridge, UK: Royal Society of Chemistry, 2002.

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Saul, Patai, Rappoport Zvi, and Stirling C. J. M, eds. The Chemistry of sulphones and sulphoxides. Chichester [Sussex]: Wiley, 1988.

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Chokusa arukirubenzen suruhon-san oyobi sono shio (arukiru-ki no tansosū ga 10 kara 14 made no mono oyobi sono kongōbutsu ni kagiru): Linear alkylbenzene sulfonic acid and its salt. Tōkyō-to Shibuya-ku: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.

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Patai, Saul, and Zvi Z. Rappoport. Chemistry of Sulphonic Acids, Esters and Their Derivatives. Wiley & Sons, Limited, John, 2006.

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Sulfanilic acid from the Republic of Hungary and India: Determination of the Commission in investigation no. 701-TA-318 (preliminary) under the Tariff Act of 1930, together with the information obtained in the investigation : determinations of the Commission in investigations nos. 731-TA-560 and 561 (preliminary) under the Tariff Act of 1930, together with the information obtained in the investigations. Washington, D.C: U.S. International Trade Commission, 1992.

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Sulfanilic acid: Probable economic effect of removal from the list of eligible articles under the U.S. generalized system of preferences : report to the President on Investigation No. 332-330. Washington, DC: U.S. International Trade Commission, 1992.

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Sulfanilic acid from the Republic of Hungary and India: Determination of the Commission in investigation no. 701-TA-318 (final) under the Tariff Act of 1930, together with the information obtained in the investigation : determinations of the Commission in investigations nos. 731-TA-560 and 561 (final) under the Tariff Act of 1930, together with the information obtained in the investigations. Washington, DC: U.S. International Trade Commission, 1993.

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Beilstein Handbook of Organic Chemistry: Supplement 5: Heterocyclic Compounds with One Ring-Nitrogen Atom: Carboxylic Acids, Sulfonic Acids, Amines Etc. Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, 1990.

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Book chapters on the topic "Sulfonic acids"

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Peter, L. B. "Sulfonic Acids, Salts and Esters." In Inorganic Reactions and Methods, 20–21. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch25.

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Alberti, Giulio, Riccardo Narducci, and Maria Luisa Di Vona. "Perfluorinated Sulfonic Acids as Proton Conductor Membranes." In Solid State Proton Conductors, 295–329. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781119962502.ch8.

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Csapó, J., I. Tóth-Pósfai, and Z. S. Csapó-Kiss. "Separation of D- and L-amino acids by ion exchange column chromatography in the form of 2-sulfonic acid alanyl dipeptides." In Amino Acids, 96–101. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_12.

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Bedford, C. T. "Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives." In Organic Reaction Mechanisms Series, 47–68. Chichester, UK: John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9780470975800.ch2.

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Bedford, C. T. "Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives." In Organic Reaction Mechanisms · 2008, 45–77. Chichester, UK: John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9780470979525.ch2.

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Bedford, C. T. "Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives." In Organic Reaction Mechanisms Series, 75–115. Chichester, UK: John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9781119972471.ch2.

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Bedford, C. T. "Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives." In Organic Reaction Mechanisms Series, 67–96. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118560273.ch2.

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Bedford, C. T. "Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and Their Derivatives." In Organic Reaction Mechanisms 2001, 43–121. Chichester, UK: John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/0470866748.ch2.

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Bedford, C. T. "Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives." In Organic Reaction Mechanisms Series, 55–78. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781119941910.ch2.

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Bedford, C. T. "Reactions of Carboxylic, Phosphoric and Sulfonic Acids and their Derivatives." In Organic Reaction Mechanisms Series, 45–103. Chichester, UK: John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/0470022051.ch2.

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Conference papers on the topic "Sulfonic acids"

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Fuchiwaki, Masaki, Kazuhiro Tanaka, and Keiichi Kaneto. "Planate Conducting Polymer Actuator and Its Application." In ASME 2006 2nd Joint U.S.-European Fluids Engineering Summer Meeting Collocated With the 14th International Conference on Nuclear Engineering. ASMEDC, 2006. http://dx.doi.org/10.1115/fedsm2006-98486.

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We propose a planate conducting polymer actuator which can transform only its central part locally and a micro pump using its actuator as a drive source. We have developed a planate conducting polymer actuator based on polypyrrole and two types of acids, such as p-phenol sulfonic acid and dodecylbenzene sulfonic acid, by electrodeposition. Its structure was patterned bimorph structure with anion-driven, cation-driven and bimorph layers. The planate conducting polymer actuator could deform only its central part locally. And, we have proposed a micro pump using the planate conducting polymer actuator as the drive source. The water level in the flow channel of micro pump shows the reciprocating motion measuring ±2 mm in accordance with the oscillation of the bimorph conducting polymer actuator which was approximately 28 μl/min. The oscillating volume can be controlled by the application of electrochemical potential and its scan rate applied to the actuator.
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Zhao, Yuan-yuan, Eiji Tsuchida, Yoong-Kee Choe, Tamio Ikeshoji, and Akihiro Ohira. "A DFT Study on the Dissociation Property of Sulfonic Acids with Different Neighboring Pendants in Polymer Electrolyte Membranes." In Proceedings of Computational Science Workshop 2014 (CSW2014). Journal of the Physical Society of Japan, 2015. http://dx.doi.org/10.7566/jpscp.5.011005.

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Li, Changhai. "Adsorption of 5-Amino-2-Chlorotoluene-4-Sulfonic and Chlorhydric Acids from their solution by Weakly Basic Resin." In 2008 2nd International Conference on Bioinformatics and Biomedical Engineering (ICBBE '08). IEEE, 2008. http://dx.doi.org/10.1109/icbbe.2008.474.

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Liptak, Andras, Ferene Sajtos, and Edit Balla. "THIOGLYCOSIDE REARRANGEMENT BY 1-->2-THIO MIGRATION INTO 2-THIO SUGARS AND THEIR OXIDATION TO SUGAR 2-SULFONIC ACIDS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.610.

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Evans, William, Jazmine Eccles, and William Baldwin. "Changes in Energy Metabolism Induced by PFOS and Dietary Oxylipins." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/jnpe5541.

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CYP2B6 is a drug metabolizing cytochrome P450 (CYP) that has anti-obesity properties, but also increases non-alcoholic fatty liver disease (NAFLD) in hCYP2B6-transgenic mice compared to Cyp2b-null mice. hCYP2B6-transgenic mice are also more susceptible to perfluorooctane sulfonic acid (PFOS) toxicity, a lipid-like toxicant used in stains, varnishes and firefighting foams that increase NAFLD. Our recent research demonstrates that CYP2B6 metabolizes dietary polyunsaturated fatty acids into the oxylipins, 9-HODE and 9-HOTre, which are strong peroxisome proliferator activated receptor alpha (PPARa) agonists and weak PPARg agonists. The purpose of our studies is to better understand the mechanisms behind PFOS and oxylipin-mediated hepatic steatosis. To test whether PFOS, 9-HODE or 9-HOTrE alter mitochondrial metabolism, Seahorse Mitostress assays were performed using HepG2 cells treated with 0.2, 1 and 5mM PFOS, 9-HODE and 9-HOTrE for 24 hours (n=5). Both PFOS and 9-HOTrE increased spare respiratory capacity in a concentration-dependent manner with lesser effects by 9-HODE. qPCR was performed following exposure of HepG2 cells to 1 and 5 mM of each compound to investigate changes in gene expression that may explain alterations in mitochondrial respiration or hepatic steatosis. PFOS repressed expression of ANGPTL4, a biomarker of PPARgactivation. 9-HODE induced CD36 and FASN expression, genes involved in fatty acid uptake and synthesis. 9-HOTrE induced SREBF1 and Cpt1a expression, genes involved in sterol synthesis and fatty acid transport into the mitochondria and may partially explain the increase in SRC. Thus, based on current results, PFOS is associated with reduced transport of lipids from the liver and 9-HODE increases lipid uptake; both would increase steatosis through different mechanisms. 9-HOTre may increase metabolism and therefore reduce steatosis.
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Dekamin, Mohammad G., and Amene Yaghoubi. "Periodic Mesoporous Organosilica Functionalized Sulfonic Acids (PMO-ICS-SO3H) as an Efficient and Recyclable NanoCatalyst for the Unsymmetric Hantzsch reaction." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a012.

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"Plasticizing Characteristics of Sulfonic Acid Polymer Containing Methacrylic Acid Derivatives." In SP-148: Fourth CANMET/ACI International Conference on Superplasticizers and chemical admixtures in Concrete. American Concrete Institute, 1994. http://dx.doi.org/10.14359/4112.

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Lu, Yi Heng, Shuang Chun Ma, Ying Chen, and Wen Quan Feng. "Perfluorinated sulfonic acid ion-exchange membrane doped silicotungstic acid thermal stability and conductivity." In 2015 International Conference on Advanced Engineering Materials and Technology. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/icaemt-15.2015.139.

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Poonsawat, Worapong, Sirilux Poompradub, and Chawalit Ngamcharussrivichai. "Preparation of sulfonic acid-containing rubbers from natural rubber vulcanizates." In International Conference on Experimental Mechanics 2013 and the Twelfth Asian Conference on Experimental Mechanics, edited by Somnuk Sirisoonthorn. SPIE, 2014. http://dx.doi.org/10.1117/12.2054228.

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Takeuchi, N., R. Oishi, Y. Kitagawa, and K. Yasuoka. "Adsorption and decomposition of perfluorooctane sulfonic acid on plasma-water interface." In 2011 IEEE 38th International Conference on Plasma Sciences (ICOPS). IEEE, 2011. http://dx.doi.org/10.1109/plasma.2011.5993106.

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Reports on the topic "Sulfonic acids"

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Willenbring, Robert. Synthesis and characterization of some SF₅- containing sulfonic acids. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.5618.

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Terjeson, Robin. The Chemistry of Sulfonyl Fluorides: SF5 and/or SO2F Containing Compounds as Precursors to Sulfonic Acids. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.1240.

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Hamel, Nicolas. Monomeric and Polymeric Fluoroalkyl Sulfonyl Fluorides, Sulfonate Salts and Sulfonic Acids for Use as Electrolytes and Coatings. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.1264.

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Litt, Morton. Poly(p-Phenylene Sulfonic Acids). PEMs with frozen-in free volume. Office of Scientific and Technical Information (OSTI), January 2016. http://dx.doi.org/10.2172/1236792.

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Mohtasham, Javid. Fluorinated [beta]-sultones as Precursors to Fluorinated Sulfonic Acids, and New Fluorosulfonyl Containing Monomers/Polymers. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.1249.

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Wagener, Ken. Precision Morphology in Sulfonic, Phosphonic, Boronic, and Carboxylic Acid Polyolefins. Fort Belvoir, VA: Defense Technical Information Center, November 2013. http://dx.doi.org/10.21236/ada606523.

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Allen, H. C., E. A. Raymond, and G. L. Richmond. Surface Structural Studies of Methane Sulfonic Acid at Air/Aqueous Solution Interfaces using Vibrational Sum Frequency Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, July 2000. http://dx.doi.org/10.21236/ada379636.

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PFAS Exposure Assessments Final report. Agency for Toxic Substances and Disease Registry (ATSDR), September 2022. http://dx.doi.org/10.15620/cdc:122063.

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"PFAS (or per- and polyfluoroalkyl substances) are a family of synthetic chemicals that have been used in industry and consumer products since the 1940s. There are thousands of different PFAS. The exposure assessments (EAs) described in this report evaluated some of the most commonly studied PFAS, such as perfluorooctanoic acid (PFOA), perfluorooctane sulfonic acid (PFOS), perfluorohexane sulfonic acid (PFHxS), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoroundecanoic acid (PFUnA), and N-methyl perfluorooctanesulfonamidoacetic acid (MeFOSAA)"
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NTP Technical Report on the Toxicity Studies of Perfluoroalkyl Sulfonates (Perfluorobutane Sulfonic Acid, Perfluorohexane Sulfonate Potassium Salt, and Perfluorooctane Sulfonic Acid) Administered by Gavage to Sprague Dawley (Hsd:Sprague Dawley SD) Rats. NIEHS, August 2019. http://dx.doi.org/10.22427/ntp-tox-96.

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