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Artykuły w czasopismach na temat "High Oxidation State of Copper"
Kondo, Yasumitsu. "Behaviour of Copper and Nickel during High Temperature Oxidation of Steel Containing Them". Materials Science Forum 522-523 (sierpień 2006): 53–60. http://dx.doi.org/10.4028/www.scientific.net/msf.522-523.53.
Pełny tekst źródłaStadt, Michael Georg, Michael Nelhiebel, Silvia Larisegger i Guenter Fafilek. "In-Situ Raman Spectroscopy of Defined Copper Oxide Surfaces Formed by Electrochemically Controlled High-Temperature Oxidation". ECS Meeting Abstracts MA2023-01, nr 46 (28.08.2023): 2490. http://dx.doi.org/10.1149/ma2023-01462490mtgabs.
Pełny tekst źródłaAnamaria, Imre, Augustin Mot i Radu Silaghi-Dumitrescu. "Exploring the possibility of high-valent copper in models of copper proteins with a three-histidine copper-binding motif". Open Chemistry 10, nr 5 (1.10.2012): 1527–33. http://dx.doi.org/10.2478/s11532-012-0069-3.
Pełny tekst źródłaBera, J. K., A. G. Samuelson i J. Chandrasekhar. "Structure and energetics of high oxidation state copper fragments: Anab initio study". Proceedings / Indian Academy of Sciences 108, nr 3 (czerwiec 1996): 333. http://dx.doi.org/10.1007/bf02870100.
Pełny tekst źródłaKowalska, J., i C. S. Gopinath. "Mapping of Copper Oxidation State Using High Pressure X-Ray Photoelectron Spectroscopy". Acta Physica Polonica A 125, nr 4 (kwiecień 2014): 1065–66. http://dx.doi.org/10.12693/aphyspola.125.1065.
Pełny tekst źródłaCosta, Gabriel F., Maria Rodrigues Pinto, Igor Messias, Joao Junior, Nirala Singh i Raphael Nagao. "Tracking Copper Oxidation State during Nitrate Electrochemical Reduction Reaction". ECS Meeting Abstracts MA2023-01, nr 39 (28.08.2023): 2300. http://dx.doi.org/10.1149/ma2023-01392300mtgabs.
Pełny tekst źródłaZelinka, Samuel L., Grant T. Kirker, George E. Sterbinsky i Keith J. Bourne. "Oxidation states of copper in preservative treated wood as studied by X-ray absorption near edge spectroscopy (XANES)". PLOS ONE 17, nr 1 (27.01.2022): e0263073. http://dx.doi.org/10.1371/journal.pone.0263073.
Pełny tekst źródłaYang, Peng, Xingye Guo, Dingyong He, Zhen Tan, Wei Shao i Hanguang Fu. "Selective Laser Melting of High Relative Density and High Strength Parts Made of Minor Surface Oxidation Treated Pure Copper Powder". Metals 11, nr 12 (23.11.2021): 1883. http://dx.doi.org/10.3390/met11121883.
Pełny tekst źródłaUhlmann, Eckart, Julian Polte, Jan Streckenbach, Ngoc Chuong Dinh, Sami Yabroudi, Mitchel Polte i Julian Börnstein. "High-Performance Electro-Discharge Drilling with a Novel Type of Oxidized Tool Electrode". Journal of Manufacturing and Materials Processing 6, nr 5 (1.10.2022): 113. http://dx.doi.org/10.3390/jmmp6050113.
Pełny tekst źródłaLoucks, Robert R., Gonzalo J. Henríquez i Marco L. Fiorentini. "Zircon and Whole-Rock Trace Element Indicators of Magmatic Hydration State and Oxidation State Discriminate Copper Ore-Forming from Barren Arc Magmas". Economic Geology 119, nr 3 (1.05.2024): 511–23. http://dx.doi.org/10.5382/econgeo.5071.
Pełny tekst źródłaRozprawy doktorskie na temat "High Oxidation State of Copper"
Wang, Guanqi. "Etat d'oxydation élevé des complexes de cuivre de type galactose oxydase pour l'oxydation biomimétique de l'alcool". Electronic Thesis or Diss., Université Grenoble Alpes, 2023. http://www.theses.fr/2023GRALV106.
Pełny tekst źródłaGalactose Oxidase (GOase), a copper-containing metallo-enzyme, is one of the most studied biocatalysts for the enzymatic oxidation of carbohydrates. The consensus mechanism involves the key oxidized form (GOaseox), in which an the carbohydrate substrate (galactose unit) binds to the equatorial (free) site and is subsequently deprotonated. It undergoes hydrogen atom abstraction by the radical and further electron transfer to give the final product aldehyde and the reduced form of the GOase. Due to the potential for highly selective catalytic oxidations, the development of small-molecular models of the GOase active site has been carried out. Notably, sterically hindered schiff bases, which stand as one of the most representative mimics, have garnered significant attention. This biomimetic approach has extended to encompass other strategies. Within this framework, a range of Cu(II)-phenol complexes, serving as pre-catalysts, have been synthesized, subsequently undergoing one-electron oxidation to yield the "active" catalyst form. A central question then arises: What factors determine whether the oxidation pathway proceeds toward the ligand, resulting in the formation of Cu(II)-phenoxyl radicals, or toward the metal, giving rise to the Cu(III)-phenolate species? Despite substantial efforts, a definitive answer to this question has yet to be obtained.The aim of this thesis is to develop redox-active ligands aimed at understanding the factors affecting the oxidation state of copper, able to catalyze the oxidation of an alcohol into an aldehyde. The strategy is to include chemical functions that can stabilize either valence tautomer (Cu(II)-phenoxyl radical and Cu(III)-phenolate) and study their effect. For that purpose, several complexes were synthesized and characterized by different ways to understand their properties. The catalytic activities were also tested against different families of substrates comprising hydroxyl functions. Finally, quantum chemistry (DFT) calculations have been carried to help understand the characteristics of different complexes and elucidate of the catalytic mechanisms at work
King, Lawrence. "High oxidation state group VI imido metallasiloxanes". Thesis, Queen Mary, University of London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369235.
Pełny tekst źródłaMonaghan, Dermot. "High rate unbalanced magnetron sputtering of thick films of ultra-fine brained OFHC copper and copper alloys". Thesis, University of Salford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336163.
Pełny tekst źródłaMcFadzean, Belinda Julie. "The kinetics and associated equilibria of high oxidation state osmium complexes". Thesis, Nelson Mandela Metropolitan University, 2007. http://hdl.handle.net/10948/732.
Pełny tekst źródłaPearson, Stephen. "High oxidation state carbene complexes for C-H bond activation catalysis". Thesis, University of Edinburgh, 2010. http://hdl.handle.net/1842/7570.
Pełny tekst źródłaDann, Sandra Elizabeth. "Preparation and characterisation of high oxidation state compounds of transition metals". Thesis, University of Southampton, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241254.
Pełny tekst źródłaBenham, Emmanuel Jakob. "Actinide chemistry : high oxidation-state uranium fluoride and fluoride halide complexes". Thesis, University of Leicester, 1992. http://hdl.handle.net/2381/33962.
Pełny tekst źródłaSpicer, M. D. "Higher oxidation state complexes of group Vb and VIb donor atom ligands : Compounds with cobalt(III) and copper(III)". Thesis, University of Southampton, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.382971.
Pełny tekst źródłaHarbron, S. K. "Studies in the high oxidation state coordination chemistry of osmium and iron". Thesis, University of Southampton, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234174.
Pełny tekst źródłaSingh, Rojendra. "Cyclopropene polymerization and enyne metathesis catalyzed by high oxidation state molybdenum alkylidenes". Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43771.
Pełny tekst źródłaVita.
Includes bibliographical references.
Chapter 1. An olefin metathesis reaction between Mo(NAr)(CHCMe2Ph)(OCMe(CF3)2)2 (Ar = 2,6diisopropylphenyl) and trans-i 1,4-divinylbenzene or trans, trans- 1,4-di-buta- 1,3-dienylbenzene (5) results in the formation of bimetallic ROMP initiators [(DME)((CF3)2MeCO)2(ArN)MoCH]2-1,4-C6H4 (DME = 1,2-dimethoxyethane; la) and [(DME)((CF3)2MeCO)2(ArN)MoCHCHCH]2-1,4-C6H4 (6), respectively. An X-ray study of [(THF)((CF3)2MeCO)2(ArN)MoCH]2-1,4-C6H4 (THF = tetrahydrofuran; ib), which is closely related to la, showed it to be the expected bimetallic species in which each end is approximately a trigonal bipyramidal monoadduct of a syn alkylidene with the THF coordinated to the NOO face of the metal trans to the Mo=C bond. Treatment of la with hium-t-butoxide yielded [(Bu-t-O)2(ArN)MoCH]2-1,4-C6H4 (2). Addition of four equivalents of Me3CCH2MgCl to la produced the bimetallic species [(Me3CCH2)2(ArN)MoCH]2- 1,4-C6H4 (3), which upon treatment with 2,6diisopropylphenol generated a diastereomeric mixture of [(DME)(ArO)(Me3CCH2)(ArN)MoCH]2-1,4-C6H4 (4). The solid state structure of 3 revealed a "syn/syn" bimetallic species related to lb. In solution two resonances can be observed in the alkylidene region of the 1H NMR spectra for the "syn/anti" isomer of la, Ib, 2, 3, 4 and 5. The total amount of the "syn/anti" isomer varies between 4 and 20% of the total. Bimetallic species la, 2, and 6 initiate at both ends upon addition of less than ten equivalents of 4,5-dicarbomethoxynorbornadiene (DCMNBD),and afford homopolymers of DCMNBD and methyltetracyclododecene (MTD) in a living fashion. MALDI-TOF mass spectra of ferrocene-containing homopolymers have been obtained that are consistent with the polymerization process being living.
(cont.) Triblock copolymers MTDxDCMNBDyMTDx were prepared by adding y equivalents of DCMNBD to the bimetallic ROMP initiators followed (after consumption of DCMNBD) by 2x equivalents of MTD. These triblocks were shown to be of relatively high purity (free of homopolymer and diblock copolymer) and to have a relatively low polydispersity index. Chapter 2 A series of monomers with side chain liquid crystals (SCLCs) were synthesized for ring opening metathesis polymerization (ROMP). The liquid crystals (LCs) used were 4hydroxybenzoic acid 4-methoxyphenyl ester (MPOB-H), which is known to exhibit a nematic liquid crystalline phase, and biphenyl-4-carboxylic acid 4-(1butoxycarbonylethoxy)phenyl ester (BPP4-H), which is known to exhibit a smectic phase. The side chains differed in spacer length, spacer type, and the nature of the LC. Monomers were polymerized using a bimetallic ROMP initiator [(Bu-t-O)2(ArN)MoCH]2-1,4-C6H4 (where Ar = 2,6-diisopropylphenyl); both homopolymers and ABA type triblock copolymers, where the B block is the LC functional monomer, and A is methyltetracyclodocene (MTD) were prepared. The polymers displayed unimodal peak distributions with polydispersities < 1.22. Incorporation of a polyoxyethylene spacer decreased the glass transition temperature (Tg) of the polymer block to -25 from +20 TC, the Tg when an alkyl spacer was used. Although no distinct LC phase was observed with the polyoxyethylene spacer when MPOB was used, use of BPP4 in conjunction with a polyoxyethylene spacer displayed a distinct liquid crystalline transition. Polymers with an alkyl spacer exhibited liquid crystalline behavior and good phase segregation on the basis of differential scanning calorimetry and small-angle X-ray scattering studies.
(cont.) Chapter 3. Molybdenum imido alkylidene complexes supported by 2,6-diisopropylphenyl, 2,6dimethylphenyl, 1-adamantyl, or 2-trifluorophenyl that contain relatively electronwithdrawing phenolate (pentafluoro), binaphtholate (3,3'-bis(9-anthracenyl), 3,3'bispentafluorophenyl, or 3,3'-bis(3,5-bis(trifluoromethyl)phenyl)) or biphenolate (3,3'-ditert-butyl-5,5'-bistrifluoromethyl-6,6'-dimethyl-1,1'-biphenyl) ligands have been prepared to be tested in olefin metathesis reactions. A series of new monomeric pyrrolide complexes, Mo(NR)(CHCMe2R')(2,5-dimethylpyrrolide)2 (where R' = Me or Ph) and Mo(NAd)(CHCMe2Ph)(2,4-dimethylpyrrolide)2, were also synthesized and treated with alcohols, biphenols or binaphthols in order to generate Mo(NR)(CHCMe2Ph)(diolate) species. In several cases the new alkylidene complexes could be prepared only through reaction of two equivalents of pentafluorophenols or an equivalent of binaphthol (3,3'bis(pentafluorophenyl)binaphthol or 3,3'-bis(3,5-bis(trifluoromethyl)phenyl binaphthol) with a bis(2,5-dimethylpyrrolide) complex. The pyrrolide approach can be employed either to isolate catalysts on a preparative scale or to generate catalysts in situ. Several simple preliminary ring-closing metathesis reactions show that the new complexes are catalytically competent. Chapter 4. Living ring opening metathesis polymerization of cyclopropenes using Mo(NAr)(CHCMe2R)(O-t-Bu)2 (where R = Me; la or R = Ph; ib) and Mo(NAr)(CHCMe2Ph)(OCMe(CF3)2)2 (2) has been achieved. The polydispersity indices of the polymers generated are recorded to be < 1.10 for la and lb based on gel permeation chromatography (GPC). Living polymerization of 3-methyl-3phenylcyclopropene (MPC) by t-butoxide derived molybdenum imido alkylidene initiators is utilized in the synthesis of block copolymers.
(cont.) Diblock copolymers MPCPxDCMNBDy (where DCMNBD = 2,3- dicarbomethoxynorbornadiene and x and y are the number of equivalents of MPC and DCMNBD, respectively) were prepared in quantitative yield with unimodal peak distribution via sequential addition of monomers to the initiator 1b. Triblock copolymers MPC100MEMC100MPCoo0 and MTDiooMEMCIooMTDjoo were prepared using [(O-t-Bu)2(ArN)MoCH]2-1,4-C6H4 (IC) as an initiator. The block copolymers revealed good phase segregation based on the differential scanning calorimetry (DSC). ROMP of MPC by molybdenum imido alkylidene initiators containing electron-withdrawing diolates resulted in highly tactic polymers as determined by 'H and 13C NMR spectroscopy. IR spectroscopy of all MPCl00 revealed absorptions at 963 and/or 982 cm-1 of approximately equal intensity that are most consistent with a trans structure. Chapter 5. Addition of one equivalent of ROH to Mo(NAr)(CHCMe2Ph)(2,5-dimethylpyrrolide)2 (Ar = 2,6-diisopropylphenyl) in diethyl ether or THF yielded Mo(NAr)(CHCMe2Ph)(OR)(2,5-dimethylpyrrolide) species where R = (CH3)3C (1), (CH3)2CH (2), Ar (3), (CF3)2CH (4), (CF3)2MeC (5), (Bu-t-O)3SiO (6) or C6F50 (7). Treatment of an equivalent of PMe3 to 5 resulted in the formation of (Me3P)Mo(NAr)(CHCMe2Ph)(OCMe(CF3)2)(PyrMe) (Me3P-5), which showed trans binding of PMe3 with respect to 2,5-dimethylpyrrolide ligand as determined by the 'H NOESY spectrum. The solid state structure of 3 depicts a psuedo-tetrahedral geometry around the metal center with the 2,5-dimethylpyrrolide ligand bound rq' to the metal cener.
(cont.) Complexes 1-6 show rapid reaction when treated with one atmosphere of ethylene and catalyze ring-closing metathesis reactions. Hetereogenous analogs of 6, Mo(NAr)(CHCMe2Ph)(PyrMe)(OSisurf) (10a), Mo(NAd)(CHCMe2Ph)(PyrMe)(OSisurf) (10b) and Mo(NArF)(CHCMe2Ph)(PyrMe)(OSisurf) (10c) (Ad = 1-adamantyl and ArF = 2trifluoromethylphenyl) showed great enhancement in the catalytic activity when employed in self-metathesis of propene and ethyloleate. Ring-closing enyne metathesis catalyzed by 1 - 6 leads to cyclic products that arise through initial addition of the triple bond to a methylene species (initially neophylidene) to yield an cC- or a 3-substituted metallacyclobutene intermediate.
by Rojendra Singh.
Ph.D.
Książki na temat "High Oxidation State of Copper"
Whitfield, Pamela Stephenie. Chemical and diffraction studies of the copper oxidation state in cuprate superconductors. Birmingham: University of Birmingham, 1997.
Znajdź pełny tekst źródłaBarrera, Gabriel Plascencia. High temperature oxidation of copper and copper aluminium alloys: Impact on furnace side wall cooling systems. 2004.
Znajdź pełny tekst źródłaGluckman, Sir Peter, Mark Hanson, Chong Yap Seng i Anne Bardsley. Copper in pregnancy and breastfeeding. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780198722700.003.0024.
Pełny tekst źródłaCzęści książek na temat "High Oxidation State of Copper"
Schuller, Ivan K., D. G. Hinks, J. D. Jorgensen, L. Soderholm, M. Beno, K. Zhang, C. U. Segre, Y. Bruynseraede i J. P. Locquet. "Copper Oxidation States, Vacancy Ordering and Their Effect on High Temperature Superconductivity". W Novel Superconductivity, 647–52. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1937-5_73.
Pełny tekst źródłaNishiyama, Yoshitaka, i Nobuo Otsuka. "The Role of Copper in Resisting Metal Dusting of Ni-Base Alloys". W High-Temperature Oxidation and Corrosion 2005, 581–88. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-409-x.581.
Pełny tekst źródłaEl-Saadani, Mohamed, Hermann Esterbauer, Günther Jürgens, Mohamed El-Sayed, Ahmed Nassar, Mohamed Goher i Anton Holasek. "Copper and Copper-Nicotinic Acid Complexes Mediated Oxidation of High Density Lipoprotein". W Oxygen Radicals in Biology and Medicine, 381–85. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5568-7_59.
Pełny tekst źródłaLim, Byeong Soo, M. J. Jin, Si Yon Bae i Dong Bok Lee. "The Oxidation and High Temperature Fatigue of P23 Alloy". W Solid State Phenomena, 31–38. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/3-908451-15-9.31.
Pełny tekst źródłaKondo, Yasumitsu. "Behaviour of Copper and Nickel during High Temperature Oxidation of Steel Containing Them". W High-Temperature Oxidation and Corrosion 2005, 53–60. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-409-x.53.
Pełny tekst źródłaShekhter, Dr Leonid N., Dr Corby G. Anderson, Daniel G. Gribbin, Esra Cankaya-Yalcin, Joseph D. Lessard i Larry F. McHugh. "Looping Sulfide Oxidation™Process for Anode Copper Production". W 4th International Symposium on High-Temperature Metallurgical Processing, 37–44. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118663448.ch5.
Pełny tekst źródłaChen, Feng, Zhiqiao Yan i Tao Wang. "Effects of Internal Oxidation Methods on Microstructures and Properties of Al2O3 Dispersion-Strengthened Copper Alloys". W High Performance Structural Materials, 1–8. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-0104-9_1.
Pełny tekst źródłaMorawitz, H., i V. Z. Kresin. "Combined Phonon-Acoustic Plasmon Theory of High-Tc Copper Oxides". W Springer Series in Solid-State Sciences, 376–81. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-84345-7_72.
Pełny tekst źródłaRaveau, B., F. Deslandes, C. Michel, M. Hervieu, G. Heger i G. Roth. "The Solid State Chemistry of Mixed Valence Copper Oxide High Tc Superconductors". W High-T c Superconductors, 3–12. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4899-0846-9_1.
Pełny tekst źródłaRogers, Michelle M., i Shannon S. Stahl. "N-Heterocyclic Carbenes as Ligands for High-Oxidation-State Metal Complexes and Oxidation Catalysis". W N-Heterocyclic Carbenes in Transition Metal Catalysis, 21–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-36930-1_2.
Pełny tekst źródłaStreszczenia konferencji na temat "High Oxidation State of Copper"
Asadiankouhidehkordi, Golnoush, Andre C. Liberati, Fadhel Ben Ettouil i Christian Moreau. "Inner Diameter High-Velocity Air Fuel (ID-HVAF) Spraying of Copper, Compared to Cold Spray". W ITSC 2023. ASM International, 2023. http://dx.doi.org/10.31399/asm.cp.itsc2023p0531.
Pełny tekst źródłaWebb, Ralph L., Jin Wook Paek i David Pickrell. "Very High Performance Thermal Interface Material and Attachment Technology". W ASME 2003 International Electronic Packaging Technical Conference and Exhibition. ASMEDC, 2003. http://dx.doi.org/10.1115/ipack2003-35253.
Pełny tekst źródłaKatcher, Kelsi M., Timothy C. Allison, Michael Marshall, Yuin Jin, Chansun Lim i Sungho Chang. "Design of a Cooled sCO2 Combustion Test Rig for Steady-State Kinetics Testing". W ASME Turbo Expo 2021: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/gt2021-04122.
Pełny tekst źródłaWenting Zhao, Jiechen Wu, Anmin Hu, Ming Li i Dali Mao. "An investigation into copper oxidation behavior". W High Density Packaging (ICEPT-HDP). IEEE, 2010. http://dx.doi.org/10.1109/icept.2010.5582339.
Pełny tekst źródłaXiangquan Fan, Techun Wang, Yuqi Cong, Binhai Zhang i Jiaji Wang. "Oxidation study of copper wire bonding". W High Density Packaging (ICEPT-HDP). IEEE, 2010. http://dx.doi.org/10.1109/icept.2010.5582431.
Pełny tekst źródłaLee, K. I., K. I. Min, S. K. Joo, K. G. Rha i W. S. Kim. "Characteristics of the Oxidation Barrier Layers for Copper Metallization". W 1994 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1994. http://dx.doi.org/10.7567/ssdm.1994.c-11-4.
Pełny tekst źródłaTatham, D. R., Liang-Kuei Chou i K. A. Abboud. "High-oxidation state salts of BEDT-TTF". W International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835519.
Pełny tekst źródłaRotteger, Chase, i Scott Sayres. "TUNABLE EXCITED STATE DYNAMICS OF NEUTRAL COPPER OXIDE CLUSTERS WITH SIZE AND OXIDATION". W 2023 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.6998.
Pełny tekst źródłaIwaki, Chikako, Daigo Kittaka, Toshihiro Yoshii, Motoshige Yagyu, Masato Okamura, Masashi Tanabe i Fumihiko Ishibashi. "Development of Hydrogen Treatment System in Severe Accident: Part 2 — Study on Reaction Characteristic of a Hydrogen Processing Unit". W 2016 24th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icone24-60917.
Pełny tekst źródłaLee, W. L., J. L. Zhang, S. Y. Wang, M. L. Tsai, G. L. Luo i C. H. Chien. "Time-Dependent Selective Oxidation by Low Pressure Oxidation on High-Ge-Content SiGe". W 2018 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2018. http://dx.doi.org/10.7567/ssdm.2018.ps-1-22.
Pełny tekst źródłaRaporty organizacyjne na temat "High Oxidation State of Copper"
Chacon, L. C. The synthesis, characterization and reactivity of high oxidation state nickel fluorides. Office of Scientific and Technical Information (OSTI), grudzień 1997. http://dx.doi.org/10.2172/335167.
Pełny tekst źródłaLucier, George Michael. Synthesis, structure, and reactivity of high oxidation state silver fluorides and related compounds. Office of Scientific and Technical Information (OSTI), maj 1995. http://dx.doi.org/10.2172/101247.
Pełny tekst źródłaShen, Ciping. Preparations and characterizations of novel graphite-like materials and some high oxidation state fluorine chemistry. Office of Scientific and Technical Information (OSTI), listopad 1992. http://dx.doi.org/10.2172/10174522.
Pełny tekst źródłaTawfik, Aly, Deify Law, Juris Grasis, Joseph Oldham i Moe Salem. COVID-19 Public Transportation Air Circulation and Virus Mitigation Study. Mineta Transportation Institute, czerwiec 2022. http://dx.doi.org/10.31979/mti.2021.2036.
Pełny tekst źródłaTawfik, Aly, Deify Law, Juris Grasis, Joseph Oldham i Moe Salem. COVID-19 Public Transportation Air Circulation and Virus Mitigation Study. Mineta Transportation Institute, czerwiec 2022. http://dx.doi.org/10.31979/mti.2022.2036.
Pełny tekst źródłaPlouffe, A., D. Petts, I M Kjarsgaard i M. Polivchuk. Laser ablation inductively coupled plasma mass spectrometry mapping of porphyry -related epidote from south-central British Columbia. Natural Resources Canada/CMSS/Information Management, 2023. http://dx.doi.org/10.4095/331671.
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