Auswahl der wissenschaftlichen Literatur zum Thema „Alkaline Earth Metal hydrides“
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Zeitschriftenartikel zum Thema "Alkaline Earth Metal hydrides"
Yang, Wen-Hua, Wen-Cai Lu, Shan-Dong Li, Xu-Yan Xue, Wei Qin, K. M. Ho und C. Z. Wang. „Superconductivity in alkaline earth metal doped boron hydrides“. Physica B: Condensed Matter 611 (Juni 2021): 412795. http://dx.doi.org/10.1016/j.physb.2020.412795.
Der volle Inhalt der QuelleShi, Xianghui, Zhizhou Liu und Jianhua Cheng. „Research Progress of Molecular Alkaline-Earth Metal Hydrides“. Chinese Journal of Organic Chemistry 39, Nr. 6 (2019): 1557. http://dx.doi.org/10.6023/cjoc201903043.
Der volle Inhalt der QuelleReckeweg, Olaf, Jay C. Molstad, Scott Levy und Francis J. DiSalvo. „Syntheses and Crystal Structures of the New Ternary Barium Halide Hydrides Ba2H3X (X = Cl or Br)“. Zeitschrift für Naturforschung B 62, Nr. 1 (01.01.2007): 23–27. http://dx.doi.org/10.1515/znb-2007-0104.
Der volle Inhalt der QuelleKunkel, Nathalie, Holger Kohlmann, Adlane Sayede und Michael Springborg. „Alkaline-Earth Metal Hydrides as Novel Host Lattices for EuIILuminescence“. Inorganic Chemistry 50, Nr. 13 (04.07.2011): 5873–75. http://dx.doi.org/10.1021/ic200801x.
Der volle Inhalt der QuelleYvon, Klaus, und Bernard Bertheville. „Magnesium based ternary metal hydrides containing alkali and alkaline-earth elements“. Journal of Alloys and Compounds 425, Nr. 1-2 (November 2006): 101–8. http://dx.doi.org/10.1016/j.jallcom.2006.01.049.
Der volle Inhalt der QuelleZhang, Song, Lu Wang, Yun-Long Tai, Yun-Lei Teng, Juan Zhao, Wei Zhu und Bao-Xia Dong. „Metal carbonates-induced solution-free dehydrogenation of alkaline earth metal hydrides at room temperature“. Journal of Solid State Chemistry 289 (September 2020): 121485. http://dx.doi.org/10.1016/j.jssc.2020.121485.
Der volle Inhalt der QuelleGebreyohannes, Muez Gebregiorgis, Chernet Amente Geffe und Pooran Singh. „Computational study of pressurized tetragonal magnesium hydride (MgH4) as a potential candidate for high-temperature superconducting material“. Materials Research Express 9, Nr. 3 (01.03.2022): 036001. http://dx.doi.org/10.1088/2053-1591/ac5e22.
Der volle Inhalt der QuelleIVANOVIĆ, NENAD, NIKOLA NOVAKOVIĆ, DANIELE COLOGNESI, IVANA RADISAVLJEVIĆ und STANKO OSTOJIĆ. „ELECTRONIC PRINCIPLES OF SOME TRENDS IN PROPERTIES OF METALLIC HYDRIDES“. International Journal of Modern Physics B 24, Nr. 06n07 (20.03.2010): 703–10. http://dx.doi.org/10.1142/s0217979210064320.
Der volle Inhalt der QuelleKunkel, Nathalie, Holger Kohlmann, Adlane Sayede und Michael Springborg. „ChemInform Abstract: Alkaline-Earth Metal Hydrides as Novel Host Lattices for EuII Luminescence.“ ChemInform 42, Nr. 35 (04.08.2011): no. http://dx.doi.org/10.1002/chin.201135009.
Der volle Inhalt der QuelleStavila, Vitalie. „Structural features of metal dodecahydro-closo-dodecaborates“. Acta Crystallographica Section A Foundations and Advances 70, a1 (05.08.2014): C1026. http://dx.doi.org/10.1107/s2053273314089736.
Der volle Inhalt der QuelleDissertationen zum Thema "Alkaline Earth Metal hydrides"
Santoru, Antonio [Verfasser]. „Insights into the structure and reaction mechanism of alkali and alkaline-earth metal amide-metal hydride composite systems for hydrogen storage / Antonio Santoru“. Hamburg : Helmut-Schmidt-Universität, Bibliothek, 2018. http://d-nb.info/1162510706/34.
Der volle Inhalt der QuelleVerbraeken, Maarten Christiaan. „Doped alkaline earth (nitride) hydrides“. Thesis, St Andrews, 2009. http://hdl.handle.net/10023/714.
Der volle Inhalt der QuelleTreuil-Dussouet, Félix. „Photoconductivity in rare earth metal-oxy-hydrides“. Thesis, Uppsala universitet, Materialteori, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-416695.
Der volle Inhalt der QuellePianalto, Frederick Scott 1961. „Laser spectroscopy of strontium-sulfide and alkaline earth monoborohydrides“. Thesis, The University of Arizona, 1988. http://hdl.handle.net/10150/276739.
Der volle Inhalt der QuelleBlake, Matthew Paul. „Alkaline earth- and rare earth-transition metal complexes“. Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:d14f9c15-ec66-4317-82df-04d6ba1d4899.
Der volle Inhalt der QuelleHuadsai, Wimonsiri. „Activation du dioxyde de carbone par des composés de Lewis hautement acidés“. Electronic Thesis or Diss., Université de Toulouse (2023-....), 2024. http://www.theses.fr/2024TLSES053.
Der volle Inhalt der QuelleThis research aimed to investigate the potential applications of Mg and Ca hydride complexes supported by ß-diketiminate and amidinate ligands for the reduction of CO2 molecules. The catalytic abilities of these complexes were explored in the context of hydroboration and hydrosilylation of CO2. In the first part of the study, we examined the reactivity of ß-diketiminato Mg and Ca hydrides with CO2. It was observed that the Mg hydride complex rapidly incorporated CO2, leading to the formation of various intermediates with different nuclearities. This involved the insertion of Mg—H bond into CO2, resulting in the generation of formate moieties. Under heat, hexameric formate complexes were formed through a "ligand flip" mechanism, releasing steric hindrances around the metal centers. For Ca hydride and CO2 reactions, in situ NMR analysis was mainly conducted. Additionally, a novel Mg amidinate dihydride complex was successfully synthesized and reacted with CO2 to yield a unique single product of dimeric formate Mg complex, in contrast to the ß-diketiminate scaffold, where several formate species were detected. The second part of the research focused on the catalytic hydroboration of CO2 using alkaline-earth hydride complexes. In particular, the Ca-based system demonstrated high efficiency in the production of the four-electron reduction of CO2 or BBA product. This was the first example of using Mg and Ca hydride compounds to catalyze the hydroboration of CO2, selectively producing the BBA product. The in situ generated BBA was further used as a methylene transfer reagent in condensation reactions with thiols, resulting in the formation of novel stable hemithioacetal [RS—CH2—OBR2] compounds under mild and neutral conditions. Activation of the hemithioacetal compounds was achieved under acidic conditions, leading to the formation of dithioacetals and hemithioaminals. The condensation of the second OBR2 fragment with secondary amines, which act as stronger nucleophiles, resulted in the generation of aryl methyl sulfides [RS—CH2—NR2]. In the final section, we investigated the tandem hydrosilylation of CO2 using various hydrosilanes in combination with [Ae]-based hydride complexes and Lewis acid B(C6F5)3 as catalysts. This research expanded on previous studies of Mg-mediated hydrosilylation of CO2 and introduced the first example of Ca-catalyzed CO2 hydrosilylation with hydrosilanes. The effectiveness of reducing CO2 to CH4 or bis(silyl)acetal [H2C(Ph3SiO)2] or BSA depended on the nature of the silanes and the steric hindrances around the substrate Si—H bond. The choice of [Ae] catalyst also significantly influenced the overall reaction rate. Furthermore, Eyring and Arrhenius analyses provided insight into the activation parameters for reducing CO2 by certain catalysts, revealing that this reaction is primarily governed by an entropic contribution. In summary, this research has demonstrated the reactivity of Mg and Ca hydride complexes for CO2 reduction and explored their applications in hydroboration and hydrosilylation reactions. Future investigations may explore mechanistic possibilities, kinetic differences, and the reactivity of group 2 metal hydride complexes with carbon monoxide for CO homologation
Rees, David Alan. „Synthesis of alkaline earth transition metal sulfides“. Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311775.
Der volle Inhalt der QuelleLiang, Tao. „Chiral Phosphoric Acids and Alkaline Earth Metal Phosphates Chemistry“. Thesis, University of South Florida, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3632228.
Der volle Inhalt der QuelleAsymmetric synthesis and catalysis is one of the leading research areas in chemistry society, for its versatility and efficiency in obtaining chiral molecules that found the vast majority in natural active compounds and synthetic drugs. Developing asymmetric catalytic methodology is at the frontier in both industrial and academic research laboratories. Enantioselective organocatalysis has emerged as a powerful synthetic tool that is complementary to metal-catalyzed transformations. The development of chiral phosphoric acid and metal phosphate as catalysts has been a breakthrough in recent years. Chiral phosphoric acids have been shown to be powerful catalysts in many organic transformations. Moreover, chiral metal phosphates, which formed by simply replacing the proton in phosphoric acid with metals, have introduced new catalytic activations and broaden the scope of phosphoric acids. This thesis details new highly enantioselective chiral phosphoric acid-catalyzed Pinacol rearrangement and robust alkaline phosphates catalytic system, which utilizes novel carbonyl activation.
The Pinacol rearrangement has long been known to be difficult to control in terms of regioselectivity and stereoselectivity. The initial studies found that indolyl-diol compounds can be treated with chiral phosphoric acids to afford the Pinacol rearrangement with high regio- and enantioselectivity. Over 16 chiral phosphoric acids were screened, and it was found an H8-BINOL-phosphoric acid variant with 1-naphthyl groups at 3 and 3' position was the excellent catalyst. This asymmetric transformation is tolerant toward variety of substituents both on the indole ring and migrating groups.
During the study, it was found that different ways to generate the catalyst had critical effect on this catalytic transformation. Only those phosphoric acids washed with HCl after column chromatography afforded the rearrangement products with high enantioselectivity. And those without treating with HCl were found contaminated by alkaline metals. These "contamination" catalysts were also found active with carbonyl activations.
A highly enantioselective catalytic hetero-Diels-Alder reaction of alpha-keto esters has been developed with chiral alkaline metal phosphates. A calcium 1-naphthyl-BINOL phosphate was found to be the optimum catalyst. A large range of alpha-keto esters as well as isatins can be applied in this alkaline phosphates catalytic system with high efficiency and selectivity. The structure of the catalyst is detailed for the first time by X-ray crystal structure analysis. A proposed Transition state model is provided based on the catalyst crystal structure and Raman spectroscopy analysis.
This methodology was further developed with an asymmetric Mukaiyama-Michael addition of beta,gamma-unsaturated alpha-keto ester. The best catalyst was found to be a magnesium chiral phosphate. And the transformation was found capable of tolerating a wide variety of beta,gamma-unsaturated alpha-keto esters.
Hamdy, Louise. „Developing new hydrogen bonded alkaline earth metal-organic complexes“. Thesis, University of Bath, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675739.
Der volle Inhalt der QuelleGillett-Kunnath, Miriam M. „Heavy alkaline earth metal amides: Synthetic and structural investigations“. Related electronic resource: Current Research at SU : database of SU dissertations, recent titles available full text, 2008. http://wwwlib.umi.com/cr/syr/main.
Der volle Inhalt der QuelleBücher zum Thema "Alkaline Earth Metal hydrides"
Harder, Sjoerd, Hrsg. Alkaline-Earth Metal Compounds. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36270-5.
Der volle Inhalt der QuelleChee-yan, Chan, Khoo Kean H, Lepeshkov I. N und International Union of Pure and Applied Chemistry., Hrsg. Alkaline earth metal perchlorates. Oxford: Pergamon, 1989.
Den vollen Inhalt der Quelle findenHan, Qiyong. Rare earth, alkaline earth and other elements in metallurgy. Tokyo: Japan Technical Information Service, 1998.
Den vollen Inhalt der Quelle findenLange, Norbert. Schwingungsspektroskopische Untersuchungen an Erdalkali- und Übergangsmetallhalogenaten. Rheinfelden: Schäuble, 1992.
Den vollen Inhalt der Quelle findenNoble, E. G. Solubilities of chloride salts of alkali and alkaline-earth metals when sparged with hydrogen chloride. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1985.
Den vollen Inhalt der Quelle findenAnoop, Kelkar, und Bhabha Atomic Research Centre, Hrsg. Validation of ION chromatography for the determination of transition metal IONs along with alkali, alkaline earth metal elements for uranium oxide fuel. Mumbai: Bhabha Atomic Research Centre, 2009.
Den vollen Inhalt der Quelle findenAnoop, Kelkar, und Bhabha Atomic Research Centre, Hrsg. Validation of ION chromatography for the determination of transition metal IONs along with alkali, alkaline earth metal elements for uranium oxide fuel. Mumbai: Bhabha Atomic Research Centre, 2009.
Den vollen Inhalt der Quelle findenGregory, A. E. Studies leading to the development of an optical sensor for alkaline earth metal ions based on porphyrins. Manchester: UMIST, 1993.
Den vollen Inhalt der Quelle findenOrganization, World Health, Hrsg. Calcium and magnesium in drinking-water: Public health significance. Geneva, Switzerland: World Health Organization, 2009.
Den vollen Inhalt der Quelle findenMiyamoto, H., M. Salomon und H. L. Clever. Alkaline Earth Metal Halates. Elsevier Science & Technology Books, 2013.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Alkaline Earth Metal hydrides"
Papaconstantopoulos, Dimitrios A. „Alkaline Earth Hydrides“. In Band Structure of Cubic Hydrides, 75–119. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-06878-2_4.
Der volle Inhalt der QuelleGooch, Jan W. „Alkaline-Earth Metal“. In Encyclopedic Dictionary of Polymers, 27. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_428.
Der volle Inhalt der QuelleBöning, Dieter, Michael I. Lindinger, Damian M. Bailey, Istvan Berczi, Kameljit Kalsi, José González-Alonso, David J. Dyck et al. „Alkaline Earth Metal“. In Encyclopedia of Exercise Medicine in Health and Disease, 52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_4044.
Der volle Inhalt der QuelleGasik, Mikhail, Viktor Dashevskii und Aitber Bizhanov. „Alkaline Earth Metal Ferroalloys“. In Ferroalloys, 219–50. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-57502-1_12.
Der volle Inhalt der QuelleTorvisco, Ana, und Karin Ruhlandt-Senge. „Heavy Alkaline-Earth Metal Organometallic and Metal Organic Chemistry: Synthetic Methods and Properties“. In Alkaline-Earth Metal Compounds, 1–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36270-5_1.
Der volle Inhalt der QuelleWesterhausen, Matthias, Jens Langer, Sven Krieck, Reinald Fischer, Helmar Görls und Mathias Köhler. „Heavier Group 2 Grignard Reagents of the Type Aryl-Ae(L) n -X (Post-Grignard Reagents)“. In Alkaline-Earth Metal Compounds, 29–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36270-5_2.
Der volle Inhalt der QuelleJones, Cameron, und Andreas Stasch. „Stable Molecular Magnesium(I) Dimers: A Fundamentally Appealing Yet Synthetically Versatile Compound Class“. In Alkaline-Earth Metal Compounds, 73–101. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36270-5_3.
Der volle Inhalt der QuelleMulvey, Robert E., und Stuart D. Robertson. „Modern Developments in Magnesium Reagent Chemistry for Synthesis“. In Alkaline-Earth Metal Compounds, 103–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36270-5_4.
Der volle Inhalt der QuelleCarpentier, Jean-François, und Yann Sarazin. „Alkaline-Earth Metal Complexes in Homogeneous Polymerization Catalysis“. In Alkaline-Earth Metal Compounds, 141–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36270-5_5.
Der volle Inhalt der QuelleCrimmin, Mark R., und Michael S. Hill. „Homogeneous Catalysis with Organometallic Complexes of Group 2“. In Alkaline-Earth Metal Compounds, 191–241. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36270-5_6.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Alkaline Earth Metal hydrides"
Takenobu, Taishi. „Synthesis and structure of alkaline earth and rare earth metal doped C[sub 70]“. In NANONETWORK MATERIALS: Fullerenes, Nanotubes, and Related Systems. AIP, 2001. http://dx.doi.org/10.1063/1.1420133.
Der volle Inhalt der QuellePatel, Hiral, Priyank Kumar, Nisarg K. Bhatt, Pulastya R. Vyas und Vinod B. Gohel. „Phonon spectrum and dynamical elastic constants of alkaline earth metal barium“. In 3RD INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC-2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0001324.
Der volle Inhalt der QuelleSato, Yukinori. „Photoabsorption studies of quasimolecules of alkaline-earth and related metal atoms“. In Proceedings of the 12th International conference on spectral line shapes. AIP, 1995. http://dx.doi.org/10.1063/1.47463.
Der volle Inhalt der QuelleSLÍVA, Aleš, Jaromír DRÁPALA und Robert BRÁZDA. „Innovation of apparatus for processing metals of loose nature tending to air oxidation, especially alkaline earth metals“. In METAL 2019. TANGER Ltd., 2019. http://dx.doi.org/10.37904/metal.2019.929.
Der volle Inhalt der QuelleTakahashi, Y., K. Fukuda, T. Kinoshita und T. Yabuzaki. „Liquid helium line broadening and shifts of alkaline earth and alkali metal atoms“. In Proceedings of the 12th International conference on spectral line shapes. AIP, 1995. http://dx.doi.org/10.1063/1.47434.
Der volle Inhalt der QuellePhung, Nga, Hans Köbler, Diego Di Girolamo, Thi Tuyen Ngo, Gabrielle Sousa e Silva, Ivan Mora-Seró, Bernd Rech und Antonio Abate. „Impact of Alkaline Earth Metal Doping on the Stability of Perovskite Solar Cells“. In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.036.
Der volle Inhalt der QuellePhung, Nga, Hans Köbler, Diego Di Girolamo, Thi Tuyen Ngo, Gabrielle Sousa e Silva, Ivan Mora-Seró, Bernd Rech und Antonio Abate. „Impact of Alkaline Earth Metal Doping on the Stability of Perovskite Solar Cells“. In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.036.
Der volle Inhalt der QuelleChung, Chih-Ang, Ci-Siang Lin und Ci-Jyun Ho. „Computational Study of Hydrogen Storage Performance in Metal Hydride Reactors“. In ASME 2010 10th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2010. http://dx.doi.org/10.1115/esda2010-24059.
Der volle Inhalt der QuelleTa-Ming Cheng, Geng-Te Lin, Hui-Chun Wang, Ming-Chin Cheng, Hsien-Ming Wu und Chi-Young Lee. „Modified solid phase synthesis of alkaline earth metal halide (BaFBr:Eu2+) phosphor“. In Environment (ICMREE). IEEE, 2011. http://dx.doi.org/10.1109/icmree.2011.5930520.
Der volle Inhalt der QuelleManteghi, Faranak, und Targol Rahimi Masale Nezhad. „Synthesis of an alkaline-earth metal organic frameworks (MOF) based on benzene-1,2,4,5 tetracarboxylic acid“. In The 22nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecsoc-22-05703.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Alkaline Earth Metal hydrides"
Chase, M. W. Thermodynamic properties of the alkaline earth metal hydroxides (MOH) I:. Gaithersburg, MD: National Bureau of Standards, 1987. http://dx.doi.org/10.6028/nbs.tn.1243.
Der volle Inhalt der QuelleFondeur, F. F. The Effect of Alkaline Earth Metal on the Cesium Loading of Ionsiv(R) IE-910 and IE-911. Office of Scientific and Technical Information (OSTI), Januar 2001. http://dx.doi.org/10.2172/773568.
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