Relevant bibliographies by topics / Cerium(IV) ammonium nitrate)

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Academic literature on the topic 'Cerium(IV) ammonium nitrate)'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Cerium(IV) ammonium nitrate)"

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Nair, Vijay, V. Sheeba, Sreeletha B. Panicker, Tesmol G. George, Roshini Rajan, Lakshmi Balagopal, M. Vairamani, and S. Prabhakar. "Cerium(IV) Ammonium Nitrate Induced Dimerization of Methoxystyrenes." Tetrahedron 56, no. 16 (April 2000): 2461–67. http://dx.doi.org/10.1016/s0040-4020(00)00054-5.

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Ganguly, N., A. K. Sukai, and S. De. "CERIUM(IV) AMMONIUM NITRATE MEDIATED NITRATION OF COUMARINS." Synthetic Communications 31, no. 2 (January 2001): 301–9. http://dx.doi.org/10.1081/scc-100000214.

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Takeshita, Michinori, Hirohisa Tsuzuki, and Masashi Tashiro. "Treatment of Dimethoxyparacyclophanes with Ammonium Cerium(IV) Nitrate." Bulletin of the Chemical Society of Japan 65, no. 8 (August 1992): 2076–82. http://dx.doi.org/10.1246/bcsj.65.2076.

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Nair, Vijay, Jessy Mathew, Puthuparampil P. Kanakamma, Sreeletha B. Panicker, V. Sheeba, S. Zeena, and Guenter K. Eigendorf. "Novel Cerium(IV) ammonium nitrate induced dimerization of methoxystyrenes." Tetrahedron Letters 38, no. 12 (March 1997): 2191–94. http://dx.doi.org/10.1016/s0040-4039(97)00279-7.

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Baciocchi, E., T. Del Giacco, C. Rol, and G. V. Sebastiani. "Cerium (IV) ammonium nitrate catalyzed photochemical autoxidation of alkylbenzenes." Tetrahedron Letters 26, no. 28 (January 1985): 3353–56. http://dx.doi.org/10.1016/s0040-4039(00)98296-0.

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Kumar, Atul, and Seema Pathak. "Direct-Thiocyanation of Ketones Using Cerium (IV) Ammonium Nitrate." Letters in Organic Chemistry 2, no. 8 (December 1, 2005): 745–48. http://dx.doi.org/10.2174/157017805774717373.

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Glebov, Evgeni M., Vjacheslav P. Grivin, Victor F. Plyusnin, Roman G. Fedunov, Ivan P. Pozdnyakov, Vadim V. Yanshole, and Danila B. Vasilchenko. "Photochemistry of cerium(IV) ammonium nitrate (CAN) in acetonitrile." Journal of Photochemistry and Photobiology A: Chemistry 418 (September 2021): 113440. http://dx.doi.org/10.1016/j.jphotochem.2021.113440.

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Adler, Pauline, Antoine Fadel, and Nicolas Rabasso. "Cerium(iv) ammonium nitrate mediated 5-endo-dig cyclization of α-amino allenylphosphonates to spirodienones." Chemical Communications 51, no. 17 (2015): 3612–15. http://dx.doi.org/10.1039/c5cc00281h.

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Peterson, John R., Hoang D. Do, and Andrew J. Dunham. "Cerium(IV)-induced nitration of cinnamic acids. Novel remote electrophilic substitution." Canadian Journal of Chemistry 66, no. 7 (July 1, 1988): 1670–74. http://dx.doi.org/10.1139/v88-271.

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The treatment of (E)-3,4-dimethoxycinnamic acid with ceric ammonium nitrate in trifluoroacetic acid afforded (E)-1,2-dimethoxy-4-nitro-5-(2-nitroethenyl)benzene in 79% yield. The unusual ipso substitution of the carboxylic acid moiety by a nitro functional center illustrated a new reaction manifold of cerium(IV). Six cinnamic acids were examined to ascertain the generality of the transformation. The bidentate nitrato structure of the metal salt is believed to account for the nitrating ability of this system.
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Najafpour, Mohammad Mahdi, Maryam Khoshkam, Davood Jafarian Sedigh, Ali Zahraei, and Mohsen Kompany-Zareh. "Self-healing for nanolayered manganese oxides in the presence of cerium(iv) ammonium nitrate: new findings." New Journal of Chemistry 39, no. 4 (2015): 2547–50. http://dx.doi.org/10.1039/c4nj02092h.

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Dissertations / Theses on the topic "Cerium(IV) ammonium nitrate)"

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Schollin, Mårten. "Reaction Mechanism between Chitosan and Cerium(VI) Ammonium Nitrate for Production of a Greener Poly(Vinyl Acetate) Adhesive." Thesis, KTH, Skolan för kemi, bioteknologi och hälsa (CBH), 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-290297.

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Poly(vinyl acetate) (PVAc) has a major application as an indoor wood adhesive. Low water stability is however, one of the greatest drawbacks of PVAc. By grafting PVAc from a chitosan (CS) backbone (CS-graft- PVAc) water stability of adhesive is increased while good mechanical and adhesive properties are retained. Simultaneously the percentage of bio-based content is increased. This work investigates the proposed re- action mechanisms between chitosan and cerium(IV) ammonium nitrate (CAN) which is used as an initiator for the grafting reaction. Litera- ture studies showed one dominating reaction mechanism and some not as common. The reaction mechanisms and their shortcomings are pre- sented and discussed in the report.
Poly(vinyl acetat)(PVAc) har ett stort användningsområde som ett trälim för möbler som ska användas inomhus. Den dåliga vatten stabiliteten är ett av de största problemen för användning av PVAc. Genom att ympa PVAc med chitosan(CS) (CS-graft-PVAc) kan vatten stabiliteten ökas samtidigt som en god limfunktion finns kvar och delen fossilbaserad monomer blir mindre och byts ut mot en biobaserad polymer. I detta arbete undersöks de föreslagna reaktionsmekanismerna mellan CS och cerium(IV) ammonium nitrat(CAN) som används som en katalysator för att grafta PVAc med CS. Litteraturstudier visade en dominerade reaktionsmekanism och några mindre förekommande. Reaktionsmekanis- merna och eventuella tillkortakommanden som finns gällande hur de fortlöper presenteras och diskuteras i detta arbete.
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Pan, Wen-Bin, and 潘文彬. "(I) Studies on the Chemical Constituents and Biological Activities of Tupistra chinensis (II) The Esterification, Nitration and Addition Initiated by Cerium(IV) Ammonium Nitrate." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/05658422999918207931.

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博士
高雄醫學大學
藥學研究所
91
As a result of our search for bioactive agents from traditional Chinese medicine, we have undertaken the chemical investigation the methanolic extracts of the rhizomes of Tupistra chinensis. Fifty-nine compounds, including two alkaloids, eleven flavonoids, twenty-five steroids, two lignans, one amide, sixteen benzenoids, and two other compounds, were isolated from T. chinensis and their structures were established on the basis of NMR and MS spectral data. Among them, tupichinols A-F (F3, F1, F2, F5, F9, F10), tupichigenins A-F (S12, S4, S5, S10, S13, S9), tupichinins A-I (S1, S14, S15, S16, S17, S18, S19, S20, S21), tupipregnenolone (S6), and tupichiamide (Am1) were new compounds. 5-Hydroxymatairesinol dimethyl ether (L1) was isolated for the first time from natural source. Ranmogenin A (S3), Δ25(27)-pentrogenin (S2), S17 and 4-allyl-pyrocatechol (B8) exhibited 80%, 100%, 99%, and 96% inhibition against human gastric cancer (NUGC) cancer cell lines at 50 mM, respectively. Compounds Δ25(27)-pentrogenin (S2) and S17 also showed 100% and 98% inhibition against human nasopharyngeal carcinoma (HONE-1) cancer cell lines at 50 mM, respectively. The esterification of phenylacetic acids and cis-oleic acid with primary and secondary simple alcohols, which also act as solvents using cerium(IV) ammonium nitrate (CAN) at room temperature gave phenylacetates and methyl (9Z)octadec-9-enoate. The reactions, which occur under relatively mild conditions, afforded the desired products in good to excellent yields. Simultaneous aromatic nitration and esterification of 2-hydroxyphenyl propanoic acid and 2-hydroxyphenyl acetic acid under mild conditions using CAN in methanol or in methanol/dichloromethane (4:1) at room temperature afforded the corresponding mononitro methyl esters and methyl esters in good combined yields. The 3-(2’-hydroxyphenyl) propenoic acid proceeded the intramolecular esterification reaction to afford coumarin product. 2-Hydroxyphenyl carboxylic acids in acetonitrile using CAN led to the corresponding o, p-dinitro intramolecular esterification compound as the sole product in good yield in a one-step process. The 3-(2’-hydroxyphenyl) propenoic acid did not proceed the intramolecular esterification reaction to afford coumarin product. The benzoic acids employed in methanol using CAN led to the corresponding esterification products in lower yields (20~70%). While the ortho- or para-hydroxyl benzoic acids proceeded simultaneous aromatic nitration and esterification reactions in this reaction condition. The phenols employed in acetonitrile using CAN at room temperature led to the corresponding nitration products in 10~85% yields and the regioselectivity is low. The para-cresol gave a o-nitro compound as the major product, a three-ring oxidative addition product and minor nitrated biphenyl compound. The iodophenols led to the corresponding nitration products, iodination products as well as nitrodeiodonation reaction. The hydroxyl benzoic acids led to the corresponding nitrated products as well as nitrodecarboxylated products. 1-Naphthol in acetonitrile or methanol using CAN at room temperature led to 1,4-naphthoquinone and nitrated products, while 2-naphthol in acetonitrile using CAN at room temperature gave the 1-nitro-2-naphthol. The stilbenes in methanol using CAN at room temperature can proceed the oxidative addition reaction to afford the methoxylation, nitration products as well as benzophenone. dl-1,2-dimethoxy-1,2-diphenylethane was the major product in 38%-40% yields.
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Hsu, Meng-hui, and 許孟慧. "Preparation of dihydrobenzofurans via the oxidative coupling of p-vinylphenols with cerium ammonium nitrate." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/28093610118273050940.

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碩士
高雄醫學大學
醫藥暨應用化學研究所碩士在職專班
95
In this thesis, an improved method for the preparation of dihydrobenzofurans was described. The starting materials, p-vinylphenols was prepared from the corresponding p-hydroxybenzaldehydes via crossed aldol condensation or Wittig reaction in good yields. The p-vinylphenols were then treated with respectively cerium(Ⅳ) ammomium nitrate to undergo oxidative coupling to give dihydrobenzofurans in few minutes, and in moderated yields.
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Books on the topic "Cerium(IV) ammonium nitrate)"

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Harju, Mauno E. E. Transition path selection between ammonium nitrate solid phases IV, III, and II. Helsinki: Suomalainen Tiedeakatemia, 1994.

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Book chapters on the topic "Cerium(IV) ammonium nitrate)"

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Baciocchi, E., T. Del Giacco, S. M. Murgia, and G. V. Sebastiani. "Role of Nitrate Radical in the Nitrooxylation of Alkenes by Cerium(IV) Ammonium Nitrate." In Organic Free Radicals, 193–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73963-7_96.

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Baciocchi, Enrico, and Renzo Ruzziconi. "Synthetic Applications of Substitution and Addition Reactions Promoted by Cerium(IV) Ammonium Nitrate." In Free Radicals in Synthesis and Biology, 155–85. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0897-0_14.

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Baciocchi, E., D. Intini, and C. Rol. "Kinetics and Mechanism of the Oxidation Reaction of Thioethers by Cerium(IV) Ammonium Nitrate." In Organic Free Radicals, 169–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73963-7_84.

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Carreño, M. C., and M. Ribagorda. "Using Ammonium Cerium(IV) Nitrate." In Quinones and Heteroatom Analogues, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-028-00655.

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Firouzabadi, H., and N. Iranpoor. "Using Ammonium Cerium(IV) Nitrate." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00439.

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Leung, M. k., and T. Y. Luh. "Catalyzed by Ammonium Cerium(IV) Nitrate." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00207.

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Scarso, A., and G. Strukul. "Catalyzed by Ammonium Cerium(IV) Nitrate." In Peroxides, Inorganic Esters (RO-X, X=Hal, S, Se, Te, N), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-038-00072.

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Figadère, B., and X. Franck. "Oxidation with Ammonium Cerium(IV) Nitrate." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00156.

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Aitken, R. A., and K. M. Aitken. "Using Sodium Nitrite and Ammonium Cerium(IV) Nitrate." In Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes, 1. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-041-00184.

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Hou, X. L., X. S. Peng, K. S. Yeung, and H. N. C. Wong. "Ammonium Cerium(IV) Nitrate Catalyzed Radical Dimerization." In Fully Unsaturated Small-Ring Heterocycles and Monocyclic Five-Membered Hetarenes with One Heteroatom, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-109-00162.

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Conference papers on the topic "Cerium(IV) ammonium nitrate)"

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Aoki, H., K. Watanabe, T. Iizuka, N. Ishikawa, and K. Mori. "Ruthenium Film Etching and Cleaning Process Using Cerium Ammonium Nitrate (CAN)-Nitric Acid." In 2001 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2001. http://dx.doi.org/10.7567/ssdm.2001.a-2-1.

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Mihara, Morihiro, Toshiyuki Nakazawa, Norikazu Yamada, and Gento Kamei. "Effects of Nitrate on Nuclide Solubility for Co-Location Disposal of TRU Waste and HLW." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40040.

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Part of TRU waste includes a large amount of nitrate salt, the effects of which have to be evaluated in a safety assessment of co-location disposal with high level radioactive waste (HLW). High concentrations of nitrate ions from TRU waste might affect the solubility of different radionuclides in the HLW. In the current study, the effects of nitrate salt on radionuclide solubility were investigated experimentally. Solubility experiments of important and redox sensitive radionuclides, Tc(IV), Np(IV) and Se(0), were performed using various concentrations of sodium nitrate (NaNO3) and of Np(V) in NaNO3 solutions to investigate complex formation with NO3− ions. Solubility experiments of Pd(II), Sn(IV) and Nb(V) using ammonium chloride (NH4Cl) solution were also undertaken to investigate complex formation with NH3/NH4+ ions. No significant solubility enhancement was observed for Np and Se. Tc solubility in ≥0.1 mol/dm3 NaNO3 solution increased due to oxidation by nitrate ions. An increase of Np(V) solubility was expected by the chemical equilibrium model calculation with JNC-TDB, however, solubility enhancement by complex formation of Np(V) with nitrate ions was not observed. Solubility enhancement by complex formation of Sn and Nb were also not observed, only Pd solubility was increased by complex formation with NH3/NH4+ ions.
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Nickson, Ian D., Colin Boxall, Angela Jackson, and Guy O. H. Whillock. "The Development of a Method for the Simultaneous Measurement of Cerium (IV) and Chromium (VI) Species in Nitric Acid Media." In ASME 2009 12th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2009. http://dx.doi.org/10.1115/icem2009-16124.

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The corrosion of stainless steel in nitric acid media is a major concern for the nuclear industry. Several reprocessing schemes such as PUREX (Plutonium Uranium Reduction Extraction) and UREX (Uranium Reduction Extraction) utilise nitric acid media, and an understanding of the behaviour of key chemical species in these process streams is vital if their effect on associated corrosion reactions and their rates is to be accurately assessed and quantified. This will allow for more accurate prediction of the working lifetime of any stainless steel surface in contact with the process stream in question. Two such key species that are found in nuclear process streams are cerium as Ce(IV) and chromium as Cr(VI), both of which may act as corrosion accelerants. The redox chemistry of cerium and chromium in highly active liquor (HAL) will depend on nitrous acid concentration, temperature, acidity, total nitrate and possibly the influence of other dissolved species and hence an analytical technique for the on-line measurement of these quantities would be useful for lifetime prediction and corrosion prevention. As a result of this, a strategy for the simultaneous measurement of both Ce(IV) and Cr(VI) species in the presence of other ions typically found in process streams (such as Iron, Magnesium Neodymium and Aluminium) has been developed. The work presented will discuss the design and implementation of the electrochemical techniques that we have used in the development of this strategy and in the measurement of the species in question.
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McFee, John, and Kevin Barbour. "Improved Technologies for Decontamination and Reuse of Plutonium Contaminated Gloveboxes." In ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-5003.

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The Los Alamos Large Scale Demonstration and Deployment Project (LSDDP), in support of the US Department of Energy (DOE) Deactivation and Decommissioning Focus Area (DDFA), has been identifying and demonstrating technologies to reduce the cost and risk of management of transuranic element contaminated large metal objects, i.e. gloveboxes. DOE must dispose of hundreds of gloveboxes from Rocky Flats Environmental Technology Site (RFETS), Los Alamos National Laboratory (LANL), and other DOE sites. This paper reports on the results of four technology demonstrations on decontamination of plutonium-contaminated gloveboxes with each technology compared to a common baseline technology, wipedown with nitric acid. The general objective of the demonstrations was decontamination to an alpha-emitting nuclide disintegration rate of less than 50,000 disintegrations per minute per 100 square centimeters (dpm/100 cm2), the surface activity level desired for re-application of these particular gloveboxes to a new mission. The technologies demonstrated include: • A LANL-developed electrochemical decontamination system (EDS) technique utilizing a recycled electrolyte solution to contact the glovebox surface via a small electrode fixture, which is moved from location to location until the entire metal surface is decontaminated. • A commercial three-step decontamination technology marketed by Environmental Alternatives Inc. (EAI) was demonstrated to quantify its performance relative to the baseline technology. • Cerium (IV) nitrate decontamination, previously utilized at other DOE sites and developed for application to gloveboxes at RFETS, was demonstrated to quantify its performance in this application. • A Russian-developed electrochemical decontamination (ECD) technology was monitored by the Los Alamos LSDDP for potential application in DOE. Although this decontamination activity was not an LSDDP “demonstration,” it was planned, monitored, and reported using LSDDP methodologies. Generally, the experience from these demonstrations shows that all innovative technologies perform better than the baseline, nitric acid wipedown. The goal of meeting 50,000 dpm/100 cm2 was not achieved by the baseline technology or cerium nitrate decontamination at all measured locations with the number of decontamination technologies used in the demonstration. Additional decontamination cycles were estimated for achievement of the targeted activity for cost estimating purposes. However, the actual decontamination achieved may be acceptable for LLW status at some facilities. Both electrochemical techniques are capable of decontaminating surfaces to the targeted contamination level and, if desired, can decontaminate to very low levels. The EAI technology is the best performing of the wipedown techniques, but is more costly. Table I summarizes the number of cycles the various technologies required to achieve the desired decontamination level and the associated decontamination factor.
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