Academic literature on the topic 'Alcohol oxidation'

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Journal articles on the topic "Alcohol oxidation"

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Griffith, William P., and Maria Suriaatmaja. "Studies on transition-metal nitrido and oxo complexes. Part 20. Oxoruthenates and oxo-osmates in oxidation catalysis; cis-[Os(OH)2O4]2- as a catalytic oxidant for primary amines and for alcohols." Canadian Journal of Chemistry 79, no. 5-6 (2001): 598–606. http://dx.doi.org/10.1139/v00-181.

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cis-[Os(OH)2O4]2– with [Fe(CN)6]3– and other co-oxidants has been studied as a catalytic reagent for the oxidative dehydrogenation of primary aromatic and aliphatic amines to nitriles, the oxidation of primary alcohols to carboxylic acids and of secondary alcohols to ketones. Electronic and Raman spectroscopy have been used to elucidate the nature of the oxoruthenates and oxo-osmates present in a number of reported organic oxidations catalyzed by ruthenium and osmium species.Key words: oxidation catalysis, ruthenium, osmium, amine dehydrogenation, alcohol oxidation.
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Sohilait, Hanoch J. "OXIDATION OF BENZYLIC SECONDARY ALCOHOL WITH PYRIDINIUM CHLOROCHROMATE-ALUMINA (PCC-Al2O3)." Indonesian Journal of Chemistry 8, no. 1 (2010): 91–93. http://dx.doi.org/10.22146/ijc.21658.

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In these studies, Pyridinium chlorochromate-Alumina was used for oxidation of secondary alcohols (safryl alcohol and methyleugenyl alcohol) to ketone. The oxidation of safryl alcohol with PCC-Al2O3 followed by purification by potassium bisulfite yields safryl ketone (62,92%). The oxidation of methyleugenyl alcohol with PCC-Al2O3, followed by purification by potassium bisulfite yields methyleugenyl ketone (68,04%). The elucidation of these products was analyzed by FTIR, 1H-NMR and MS. Keywords : PCC-alumina, secondary alcohols, ketone
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Mobley, Justin, John Jennings, Tonya Morgan, Axel Kiefer, and Mark Crocker. "Oxidation of Benzylic Alcohols and Lignin Model Compounds with Layered Double Hydroxide Catalysts." Inorganics 6, no. 3 (2018): 75. http://dx.doi.org/10.3390/inorganics6030075.

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Alcohol oxidation to carbonyl compounds is one of the most commonly used reactions in synthetic chemistry. Herein, we report the use of base metal layered double hydroxide (LDH) catalysts for the oxidation of benzylic alcohols in polar solvents. These catalysts are ideal reagents for alcohol oxidations due to their ease of synthesis, tunability, and ease of separation from the reaction medium. LDHs synthesized in this study were fully characterized by means of X-ray diffraction, NH3-temperature programmed desorption (TPD), pulsed CO2 chemisorption, N2 physisorption, electron microscopy, and el
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PRATIK, KUMAR SEN, SANYAL ANKAN, and KALI SEN GUPTA KALYAN. "Oxidative Behaviour of Sodium Dodecyl Sulphate towards Acid Permanganate in the Absence and Presence of Benzyl Alcohol." Journal of Indian Chemical Society Vol. 70, Apr-May 1993 (1993): 341–45. https://doi.org/10.5281/zenodo.5930097.

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Department of Chemistry, Jadavpur University, Calcutta-700 032 <em>Manuscript received 13 January 1993</em> The oxidative behaviour of sodium dodecyl sulphate (SDS) towards permanganate in the absence and presence of benzyl alcohol has been investigated in perchloric acid medium. The reaction is first order with respect to [\(MNO_4^-\)] and [SDS] in the oxidation of SDS and the rate increases with an increase in [HCIO<sub>4</sub>]. For the SDS oxidation of benzyl alcohol the reaction is first order with respect to [\(MNO_4^-\)] as well as [benzyl alcohol], but a complex order with respect to [
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Şahin, Zeynel. "Oxidation of Benzyl Alcohols by Monomeric Iron Phthalocyanine Complexes: Substituents’ Effect on Their Catalytic Performance." Celal Bayar Üniversitesi Fen Bilimleri Dergisi 21, no. 2 (2025): 100–104. https://doi.org/10.18466/cbayarfbe.1570991.

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Iron phthalocyanines tetra substituted with either electron-donating n-hexyloxy or electron-withdrawing n-hexylsulfonyl substituents were prepared and tested as oxidation catalysts for benzyl alcohol, 4-bromobenzyl alcohol, 4-methylbenzyl alcohol and 4-tert-butylbenzyl alcohol. Oxidation reactions were performed at room temperature in acetonitrile, acetone, ethanol, toluene, and the best result was obtained in acetonitrile. Oxidation of alcohols using tert-butyl hydroperoxide as an oxidant in the presence of these iron(II) phthalocyanines resulted in the production of corresponding benzaldehyd
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Babayev, Elchin, Nargiz Rahimli, Ulviyya Mammadova, and Nizami Zeynalov. "Investigation of the Properties of Unsaturated Allyl Alcohol and its Oxidation Reaction Products." Nature & Science 6, no. 9 (2024): 17–20. http://dx.doi.org/10.36719/2707-1146/48/17-20.

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Abstract Organic substances in which the -OH group is directly attached to the carbon atom are called alcohols. Unsaturated alcohols are obtained by replacing the hydrogen of ethylene or acetylene-type compounds with a hydroxyl group. Allyl alcohol, the first representative of the class of unsaturated alcohols, contains oxygen. Allyl alcohol is used in optical resins, protective glasses, paints and coatings and polymer cross-linking agents, as well as in the production of pharmaceuticals, organic chemicals, plastics, herbicides, and pesticides. In organic chemistry, alcohols can be oxidized to
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Brei, Volodymyr. "OXIDATION OF ALCOHOLS OVER CERIUM-OXIDE CATALYST: CORRELATION BETWEEN THE ACTIVATION ENERGY OF THE REACTION AND THE CHEMICAL SHIFT δ (R13 COH)". Ukrainian Chemistry Journal 85, № 8 (2019): 66–72. http://dx.doi.org/10.33609/0041-6045.85.8.2019.66-72.

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The oxidation of thirteen alcohols over sup-ported CeO2/Al2O3 catalyst with 10 wt.% of CeO2 have been studied using a desorption mass-spec-trometry technique. A catalyst sample 4–6 mg in quartz cuvette was evacuated at 100 0C, cooled to room temperature, and then adsorption of a alco-hol was provided. After vacuumation of alcohol excess, the TPR profiles of products of alcohol oxidation were recorded at sweep rate 2 a.u.m./sec and heating rate of 15 0C/min using MX-7304A monopole mass- spectrometer. Identification of formed aldehydes and ketones was provided on the bases of their characteristi
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Krishnamoorthy, Guna Sekar, та Seplapatty Kalimuthu Periyasamy. "Oxidation of α,β-Unsaturated Alcohols by Quinaldinium Fluorochromate". International Letters of Chemistry, Physics and Astronomy 5 (вересень 2013): 8–19. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.5.8.

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The kinetics of oxidation of α,β-unsaturated alcohols (allyl alcohol, Crotyl alcohol, Cinnamyl alcohol) by quinaldinium fluorochromate has been studied in aqueous acid medium at 313 K. α,β-unsaturated alcohols were converted to the corresponding acrolein, crotonaldehyde and cinnamaldehyde. The reaction is first order each in oxidant, substrate and H+. The decrease in dielectric constant of the medium increases the rate of the reaction. Increase in ionic strength by the addition of sodium perchlorate has no effect on the rate constant. There is no polymerization with acrylonitrile. The reaction
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Krishnamoorthy, Guna Sekar, та Seplapatty Kalimuthu Periyasamy. "Oxidation of α,β-Unsaturated Alcohols by Quinaldinium Fluorochromate". International Letters of Chemistry, Physics and Astronomy 5 (19 грудня 2012): 8–19. http://dx.doi.org/10.56431/p-91l939.

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The kinetics of oxidation of α,β-unsaturated alcohols (allyl alcohol, Crotyl alcohol, Cinnamyl alcohol) by quinaldinium fluorochromate has been studied in aqueous acid medium at 313 K. α,β-unsaturated alcohols were converted to the corresponding acrolein, crotonaldehyde and cinnamaldehyde. The reaction is first order each in oxidant, substrate and H+. The decrease in dielectric constant of the medium increases the rate of the reaction. Increase in ionic strength by the addition of sodium perchlorate has no effect on the rate constant. There is no polymerization with acrylonitrile. The reaction
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Abad, Alberto, Avelino Corma, and Hermenegildo García. "Supported gold nanoparticles for aerobic, solventless oxidation of allylic alcohols." Pure and Applied Chemistry 79, no. 11 (2007): 1847–54. http://dx.doi.org/10.1351/pac200779111847.

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After giving some general considerations about the specific properties of nanoparticles below 20 nm, procedures for size stabilization, and the importance of developing green alcohol oxidation reactions, catalytic data are presented showing that gold nanoparticles (3-7 nm) supported on nanoparticulated ceria (4 nm) are far more chemoselective than related palladium catalysts for the aerobic oxidation of allylic alcohols. Using palladium catalysts, in addition to minor oxidation of the alcohol functional group, we have also observed polymerization, 1-2 hydrogen shift, and hydrogenation. In cont
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Dissertations / Theses on the topic "Alcohol oxidation"

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But, Yuen-sze Tracy, and 畢婉詩. "Organocatalytic alcohol oxidation and Mitsunobu reactions." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B42182578.

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But, Yuen-sze Tracy. "Organocatalytic alcohol oxidation and Mitsunobu reactions." Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B42182578.

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Clendenning, Gráinne Margaret Ann. "Developing new Pd (ii) catalysts for alcohol oxidation." Thesis, Queen's University Belfast, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.579691.

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The selective aerobic oxidation of organic molecules has been highlighted as a fundamental and practical challenge for modem chemistry. The oxidation of alcohols is one such challenge. It is a key reaction in the synthesis of many compounds, however rarely implemented in an industrial setting. In the last 20 years Pd(II) complexes modulated with oxidatively stable ligands have emerged as a promising class of catalysts for the reaction. Such Pd(Il) ligated complexes utilise molecular oxygen as the sole oxidant producing benign by- products such as water. Although the work to date has been pione
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Choi, Heewon. "Alcohol Oxidation Reactions on Porous PtCu/C Catalysts." The Ohio State University, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=osu1405352022.

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Rogan, Luke. "Transition metal based catalysts for aerobic alcohol oxidation." Thesis, Queen's University Belfast, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.709812.

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The selective oxidation of alcohols to the corresponding carbonyl product is an important transformation. Traditionally this reaction has been carried out using stoichiometric oxidants, but such methods are highly undesirable from an environmental viewpoint. In the fine chemical and pharmaceutical industries, oxidative transformations prove problematic, and are often avoided, due to a limited number of existing chemoselective and sustainable oxidation methods. The demand for new, environmentally sustainable and efficient alcohol oxidation methods has driven academic research, and a number of s
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Kanno, Hisashi. "In situ alcohol oxidation-transformation reactions using manganese dioxide." Thesis, University of York, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270357.

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Lu, Liang. "Investigation of silica supported Pd catalysts for aerobic alcohol oxidation." Thesis, Queen's University Belfast, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675848.

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Oxidising alcohol to their corresponding carbonyl compound is still a vitally important reaction for the fine chemical and pharmaceutical industries. In this thesis the investigation of the use of Pd(II) catalysts for the oxidation of alcohols using 02 as the terminal oxidant is reported. The initial section describes the investigation of ligand effects on Pd(OAc)2 operating under homogeneous conditions. The examination into the use of different gas mixtures showed that 02/C02 was beneficial due to the formation in situ of alkylcarbonic add by the reaction between C02 and the alcohol substrate
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Pedersen, Nicolai. "Oxidation of veratryl alcohol with lignin peroxidase and nanoscale photosystems." Thesis, Uppsala universitet, Institutionen för kemi - BMC, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-355159.

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Padayachee, Diandree. "Development of electrocatalysts for glycerol oxidation." Thesis, University of Canterbury. Chemical and Process Engineering, 2013. http://hdl.handle.net/10092/8985.

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Glycerol is a very promising alternative fuel to hydrogen in fuel cells. However, the utilisation of glycerol as a fuel requires a good catalyst, due to the slow kinetics of glycerol electrooxidation. Gold has been identified as a promising catalyst due to its high activity and stability for glycerol electrooxidation – although the overpotentials are higher than on platinum and palladium. Modification of a nano-Au/C catalyst by the addition of MnO2, in an attempt to further improve the activity and lower the overpotential for glycerol oxidation, was therefore first explored. This was followed
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Hall, David Wesley. "Benzyl alcohol oxidation in a phase-transfer catalytic microporous contactor reactor." Thesis, University of Newcastle Upon Tyne, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.251004.

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Books on the topic "Alcohol oxidation"

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Cardona, Francesca, and Camilla Parmeggiani, eds. Transition Metal Catalysis in Aerobic Alcohol Oxidation. Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/9781782621652.

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Liang, Zhen-Xing, and Tim S. Zhao, eds. Catalysts for Alcohol-Fuelled Direct Oxidation Fuel Cells. Royal Society of Chemistry, 2012. http://dx.doi.org/10.1039/9781849734783.

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Haines, Alan H. Methods for the oxidation of organic compounds: Alcohols, alcohol derivatives, alkyl halides, nitroalkanes, alkyl azides, carbonyl compounds, hydroxyarenes and aminoarenes. Academic, 1988.

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Courtin, Helene L. Oxidation of allyl alcohol into glycerol by hydrogen peroxideoverTI-ZSM-5. UMIST, 1994.

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Inc, Arthur D. Little, ed. Partial oxidation for improved cold starts in alcohol-fueled engines: Phase II topical report. National Renewable Energy Laboratory, 1998.

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E, Allred Ronald, and United States. National Aeronautics and Space Administration., eds. Fiber finishes for improving interfacial thermo-oxidative stability in PMR-II-50 matrix composites: Final report for the period of October 1993 through September 1996, contract NAS3-27090. National Aeronautics and Space Administration, 1997.

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Slaich, Inderbir Kaur. The catalytic oxidation of alcohols with cerium (IV). University ofBirmingham, 1986.

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Yurdakal, Sedat. Selective photocatalytic oxidation of aromatic alcohols with titanium dioxide. Anadolu Üniversitesi, 2010.

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Markusse, Abraham Peter. Platinum catalyst deactivation and reactivation during aqueous oxidation of alcohols. Technische Universiteit Eindhoven, 2000.

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M, De Pontes, ed. Natural gas conversion IV: Proceedings of the 4th International Natural Gas Conversion Symposium, Kruger Park, South Africa, November 19-23, 1995. Elsevier, 1997.

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Book chapters on the topic "Alcohol oxidation"

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Gonzalez, Ernesto R., and Andressa Mota-Lima. "Catalysts for Methanol Oxidation." In Direct Alcohol Fuel Cells. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7708-8_2.

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Steves, Janelle E., and Shannon S. Stahl. "Copper-Catalyzed Aerobic Alcohol Oxidation." In Liquid Phase Aerobic Oxidation Catalysis: Industrial Applications and Academic Perspectives. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527690121.ch6.

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Berkessel, Albrecht. "Catalytic Oxidations with Hydrogen Peroxide in Fluorinated Alcohol Solvents." In Modern Oxidation Methods. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632039.ch4.

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Zultanski, Susan L., and Shannon S. Stahl. "NOxCocatalysts for Aerobic Oxidation Reactions: Application to Alcohol Oxidation." In Liquid Phase Aerobic Oxidation Catalysis: Industrial Applications and Academic Perspectives. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527690121.ch15.

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Lee, Adam F. "Mechanistic Studies of Alcohol Selective Oxidation." In Heterogeneous Catalysts for Clean Technology. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527658985.ch2.

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Arjona, Noé, Alejandro Arredondo-Espínola, Lorena Álvarez-Contreras, and Minerva Guerra-Balcázar. "Single-Atom Catalysts for Alcohol Oxidation Reactions." In Atomically Precise Electrocatalysts for Electrochemical Energy Applications. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-54622-8_24.

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Oppenheimer, Norman J., and Gary T. M. Henehan. "Horse Liver Alcohol Dehydrogenase-Catalyzed Aldehyde Oxidation." In Advances in Experimental Medicine and Biology. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1965-2_48.

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Gomes, Janaina Fernandes, Patricia Maria Patrizi Pratta, and Germano Tremiliosi-Filho. "Electro-oxidation of 3-Carbon Alcohols and Its Viability for Fuel Cell Application." In Direct Alcohol Fuel Cells. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7708-8_4.

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Bianchini, C. "4 Palladium-Based Electrocatalysts for Alcohol Oxidation in Direct Alcohol Fuel Cells." In Modern Aspects of Electrochemistry. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-5580-7_4.

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Ishimoto, Takayoshi, and Michihisa Koyama. "Chapter 4 Theoretical Aspects of Gold Nanocatalyst for Ethanol and Glucose Oxidation." In Nanomaterials for Direct Alcohol Fuel Cell. Pan Stanford Publishing, 2016. http://dx.doi.org/10.1201/9781315364902-5.

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Conference papers on the topic "Alcohol oxidation"

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wang, chengxia. "Binary Co3@CdS composite for photocatalytic oxidation of benzyl alcohol coupling with hydrogen generation." In Tenth International Conference on Energy Materials and Electrical Engineering (ICEMEE 2024), edited by Yuanhao Wang and Cristian Paul Chioncel. SPIE, 2024. https://doi.org/10.1117/12.3050510.

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Soriaga, Manuel P., G. M. Berry, C. Bhardwaj, et al. "Chemisorption of Organic Molecules on Metal Electrode Surfaces." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90300.

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Abstract The chemisorption of various organic functional groups from aqueous solutions onto smooth single-crystal and polycrystalline electrodes, and the resistance of the resulting monolayer intermediates towards electrochemical oxidation have been studied; these investigations were motivated by the need to understand, at the atomic level, metal passivation by monolayer organic coatings. The electrodes employed were Rh, Pd, Ir, Pt, and Au whose anodic dissolution is preceded by surface-oxide formation even in highly acidic media. Resistance towards anodic oxidation can thus be associated with
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Sanmartín-Matalobos, Jesús, Lucía Briones-Miguéns, Ana García-Deibe, Matilde Fondo, and Concepcion González-Bello. "A convenient Pd-mediated oxidation of 4-methylbenzyl alcohol." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a012.

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Da Xin, Xinyi Xu, Hongrui Wang, and Yuanyuan Gao. "Advanced oxidation of polyvinyl alcohol wastewater by O3/UV." In 2011 International Symposium on Water Resource and Environmental Protection (ISWREP). IEEE, 2011. http://dx.doi.org/10.1109/iswrep.2011.5893290.

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Gabrič, Maja, Florian Maximilian Harth, Brigita Hočevar, Miha Grilc, and Blaž Likozar. "Rhenium Catalyzed Production of Bio-Based Acrylates From Glyceric Acid." In TBMCE, International Conference on Technologies & Business Models for Circular Economy. University of Maribor Press, 2025. https://doi.org/10.18690/um.fkkt.1.2025.1.

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Bio-based glyceric acid, an oxidation product of glycerol, was converted into acrylic acid and its esters, crucial polymer precursors, using a new catalytic approach in a sustainable manner. Avoiding gaseous H2 or dangerous chemicals, the crucial step is Re-catalyzed deoxydehydration (DODH) in an alcoholic medium. In addition to being a solvent and hydrogen donor, alcohol also forms protective ester groups with acrylic and glyceric acids. This study examined several catalysts, alcohols, the presence of H2, and temperatures. Acrylic acid and methyl acrylate were produced in 72 hours with a 65%
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Francàs Forcada, Laia. "Alcohol oxidation using α-Fe2O3 and BiVO4: mechanistic and kinetic insides". У International Conference on Frontiers in Electrocatalytic Transformations. Fundació Scito, 2021. http://dx.doi.org/10.29363/nanoge.interect.2021.005.

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Odobel, Fabrice, Deborah ROMITO, Vasilis NIKOLAOU, Stéphane DIRING, Athanassios COUTSOLELOS, and Eric VAUTHEY. "Photocatalytic Benzyl Alcohol Oxidation Coupled with Hydrogen Evolution or CO2 Reduction." In MATSUS Spring 2024 Conference. FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2023. http://dx.doi.org/10.29363/nanoge.matsus.2024.254.

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Yan, Li, and Li Jing. "Studies on anti-oxidation effects of alcohol extract of Juglans Mandshurica leaves." In 2011 International Conference on Human Health and Biomedical Engineering (HHBE). IEEE, 2011. http://dx.doi.org/10.1109/hhbe.2011.6028032.

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P. Babu, Sreejith, and P. Elumalai. "Novel Co(OH)2/Au composite as electrocatalyst for alcohol electro-oxidation." In Proceedings of the International Conference on Nanotechnology for Better Living. Research Publishing Services, 2016. http://dx.doi.org/10.3850/978-981-09-7519-7nbl16-rps-123.

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Santi, Claudio, Hanane Achibat, Luca Sancineto, et al. "Explorative application of selenium catalysts in the oxidation of benzyl alcohol." In The 19th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a009.

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Reports on the topic "Alcohol oxidation"

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Thompson, Christopher. Studies of Heterogeneously Catalyzed Liquid-Phase Alcohol Oxidation on Platinum bySum-frequency Generation Vibrational Spectroscopy and Reaction Rate Measurements. Office of Scientific and Technical Information (OSTI), 2014. http://dx.doi.org/10.2172/1164214.

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Dudareva, Natalia, Alexander Vainstein, Eran Pichersky, and David Weiss. Integrating biochemical and genomic approaches to elucidate C6-C2 volatile production: improvement of floral scent and fruit aroma. United States Department of Agriculture, 2007. http://dx.doi.org/10.32747/2007.7696514.bard.

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The specific objectives of approved proposal include to: 1. Elucidate the C6-C2 biochemical pathways leading to the biosynthesis of phenylacetaldehyde, phenylethyl alcohol and phenylethyl acetate in floral tissues of ornamentally important plants, pefunia and roses. 2. Isolate and characterrze genes responsible for the production of these C6-C2 compounds and those involved in the regulation of the pathway using genomic and transcriptomic tools. 3. Determine whether altering the expression of key genes of this pathway can result in changing the aroma characteristics of flowers. Aldehydes are in
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Augustine, R. L., and L. K. Doyle. Catalytic oxidation of secondary alcohols. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7047071.

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Augustine, R. L., and L. K. Doyle. Catalytic oxidation of secondary alcohols. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10187537.

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Parshikov, Igor. Microbial Transformation of Some Ethylpyridines by Fungi. Intellectual Archive, 2022. http://dx.doi.org/10.32370/iaj.2635.

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We were observed transformation 4-ethylpyridine and 2-methyl-5-ethylpyridine by fungus Beauveria bassiana ATCC 7159. Stereoselective oxidation of methylene group leading to the optically active (-)-(1-hydroxyethyl)pyridine was shown. Besides, the hydroxylation of methyl groups and the oxidation of the heterocyclic ring in the nitrogen atom to the respective primary alcohols and N-oxides were observed
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Kanner, Joseph, Edwin Frankel, Stella Harel, and Bruce German. Grapes, Wines and By-products as Potential Sources of Antioxidants. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7568767.bard.

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Several grape varieties and red wines were found to contain large concentration of phenolic compounds which work as antioxidant in-vitro and in-vivo. Wastes from wine production contain antioxidants in large amounts, between 2-6% on dry material basis. Red wines but also white wines were found to prevent lipid peroxidation of turkey muscle tissues stored at 5oC. The antioxidant reaction of flavonoids found in red wines against lipid peroxidation were found to depend on the structure of the molecule. Red wine flavonoids containing an orthodihydroxy structure around the B ring were found highly
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Oji, L. N. Oxidative mineralization and characterization of polyvinyl alcohol for compatibility with tank farm processing chemistry. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/752185.

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Friend, Cynthia M., Martin Schmid, Andrew Crampton, et al. Molecular-scale Understanding of Selective Oxidative Transformations of Alcohols Promoted by Au and Au-based Alloys. Office of Scientific and Technical Information (OSTI), 2018. http://dx.doi.org/10.2172/1515177.

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Pesis, Edna, and Mikal Saltveit. Postharvest Delay of Fruit Ripening by Metabolites of Anaerobic Respiration: Acetaldehyde and Ethanol. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7604923.bard.

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Abstract:
The use of pretreatments for 24 h prior to storage, under anaerobic condtions, or in the presence of the natural metabolic products, acetaldehyde (AA) and ethanol, to delay fruit ripening, was found to be effective with several climacteric fruits, among them avocado, mango, peach and tomato. The delay in ripening of avocado, peach and tomato was accompanied by inhibition of ethylene production and of fruit softening. The maintenance of fruit firmness was associated with a decrease in the activities of cell-wall-degrading enzymes, including endoglucanases (Cx), polygalacturonases (PG) and b-gal
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Zauche, Timothy. Kinetics and mechanisms of the oxidation of alcohols and hydroxylamines by hydrogen peroxide, catalyzed by methyltrioxorhenium, MTO, and the oxygen binding properties of cobalt Schiff base complexes. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/770652.

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