Relevant bibliographies by topics / Transition metal hydrides – Synthesis

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
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Academic literature on the topic 'Transition metal hydrides – Synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Transition metal hydrides – Synthesis"

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Scheler, T., O. Degtyareva, C. Guillaume, J. Proctor, S. Evans, and E. Gregoryanz. "High-pressure synthesis of transition metal hydrides." Acta Crystallographica Section A Foundations of Crystallography 67, a1 (August 22, 2011): C57. http://dx.doi.org/10.1107/s0108767311098655.

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Liu, Yuchen, Djafar Chabane, and Omar Elkedim. "Intermetallic Compounds Synthesized by Mechanical Alloying for Solid-State Hydrogen Storage: A Review." Energies 14, no. 18 (September 13, 2021): 5758. http://dx.doi.org/10.3390/en14185758.

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Hydrogen energy is a very attractive option in dealing with the existing energy crisis. For the development of a hydrogen energy economy, hydrogen storage technology must be improved to over the storage limitations. Compared with traditional hydrogen storage technology, the prospect of hydrogen storage materials is broader. Among all types of hydrogen storage materials, solid hydrogen storage materials are most promising and have the most safety security. Solid hydrogen storage materials include high surface area physical adsorption materials and interstitial and non-interstitial hydrides. Among them, interstitial hydrides, also called intermetallic hydrides, are hydrides formed by transition metals or their alloys. The main alloy types are A2B, AB, AB2, AB3, A2B7, AB5, and BCC. A is a hydride that easily forms metal (such as Ti, V, Zr, and Y), while B is a non-hydride forming metal (such as Cr, Mn, and Fe). The development of intermetallic compounds as hydrogen storage materials is very attractive because their volumetric capacity is much higher (80–160 kgH2m−3) than the gaseous storage method and the liquid storage method in a cryogenic tank (40 and 71 kgH2m−3). Additionally, for hydrogen absorption and desorption reactions, the environmental requirements are lower than that of physical adsorption materials (ultra-low temperature) and the simplicity of the procedure is higher than that of non-interstitial hydrogen storage materials (multiple steps and a complex catalyst). In addition, there are abundant raw materials and diverse ingredients. For the synthesis and optimization of intermetallic compounds, in addition to traditional melting methods, mechanical alloying is a very important synthesis method, which has a unique synthesis mechanism and advantages. This review focuses on the application of mechanical alloying methods in the field of solid hydrogen storage materials.
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Raje, Sakthi, and Raja Angamuthu. "Solvent-free synthesis and reactivity of nickel(ii) borohydride and nickel(ii) hydride." Green Chemistry 21, no. 10 (2019): 2752–58. http://dx.doi.org/10.1039/c8gc04058c.

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Transition metal-hydrides are highly useful in organic transformations of industrial importance yet synthesizing them or their precursor metal-borohydrides in high yield is cumbersome due to their high reactivity and sensitivity towards air and many common solvents.
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Bibienne, Thomas, Roxana Flacau, Jean-Louis Bobet, and Jacques Huot. "Study of Ti-V-Cr metal hydrides by neutron powder diffraction." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1762. http://dx.doi.org/10.1107/s2053273314082370.

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Metal hydrides are interesting materials from a fundamental as well as practical point of view. In particular, Ti-based BCC solid solutions are considered as promising candidates for mobile applications because of their high volumetric capacities and room temperature operation. However, the slow kinetics of the first hydrogenation, the so-called activation step, is an important hurdle in the use of these alloys for practical applications. It has recently been shown that doping a Ti-V-Cr composition with Zr7Ni10 leads to a fast activation kinetic without heating treatment [1]. We studied the effect of this doping on two new Ti-V-Cr compositions: 52Ti-12V-36Cr and 42Ti-21V-37Cr. Two different doping methods were investigated: i) a single-melt synthesis where the raw materials (i.e. Ti, V, Cr, Zr and Ni) chunks were mixed and arc-melted; ii) co-melt synthesis where 52Ti-12V-36Cr and 7Zr-10Ni were arc-melted independently and thereafter re-melted together. Using only X-ray diffraction for structural identification does not provide information about hydrogen localization. Therefore, neutron diffraction is essential for complete determination of this class of hydrides. The peculiarity of the present alloys is that, for neutron diffraction, the scattering lengths of the elements almost cancel. Therefore, the neutron pattern of as-cast alloy shows very small Bragg peaks but the advantage is that the hydride is very easy to see and analyze. We performed in-situ neutron diffraction experiments during dehydrogenation of these materials to see the transition from the dihydride to monohydride. These measurements were complementary to X-ray and synchrotron radiation diffraction and enabled a better crystal structure determination of these alloys
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Auffermann, Gudrun, and Welf Bronger. "Synthesis and Characterization of New Ternary Hydrides with Complex Transition Metal Hydrogen Groups*." Zeitschrift für Physikalische Chemie 1, no. 1 (January 1992): 337–38. http://dx.doi.org/10.1524/zpch.1992.1.1.337.

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Nakao, Takuya, Tomofumi Tada, and Hideo Hosono. "Transition Metal-doped Ru Nanoparticles Loaded on Metal Hydrides for Efficient Ammonia Synthesis from First Principles." Journal of Physical Chemistry C 124, no. 2 (December 23, 2019): 1529–34. http://dx.doi.org/10.1021/acs.jpcc.9b10544.

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Dolukhanyan, S. K., A. G. Aleksanyan, V. Sh Shekhtman, H. G. Hakobyan, D. G. Mayilyan, N. N. Aghadjanyan, K. A. Abrahamyan, N. L. Mnatsakanyan, and O. P. Ter-Galstyan. "Synthesis of transition metal hydrides and a new process for production of refractory metal alloys: An autoreview." International Journal of Self-Propagating High-Temperature Synthesis 19, no. 2 (June 2010): 85–93. http://dx.doi.org/10.3103/s1061386210020020.

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Spektor, Kristina, Wilson A. Crichton, Stanislav Filippov, Sergei I. Simak, Andreas Fischer, and Ulrich Häussermann. "Na3FeH7 and Na3CoH6: Hydrogen-Rich First-Row Transition Metal Hydrides from High Pressure Synthesis." Inorganic Chemistry 59, no. 22 (November 3, 2020): 16467–73. http://dx.doi.org/10.1021/acs.inorgchem.0c02294.

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Mazighi, Khaled, Patrick J. Carroll, and Larry G. Sneddon. "Transition metal promoted reactions of boron hydrides. 13. Platinum catalyzed synthesis of 6,9-dialkyldecaboranes." Inorganic Chemistry 32, no. 10 (May 1993): 1963–69. http://dx.doi.org/10.1021/ic00062a015.

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Humphries, Terry D., Shigeyuki Takagi, Guanqiao Li, Motoaki Matsuo, Toyoto Sato, Magnus H. Sørby, Stefano Deledda, Bjørn C. Hauback, and Shin-ichi Orimo. "Complex transition metal hydrides incorporating ionic hydrogen: Synthesis and characterization of Na2Mg2FeH8 and Na2Mg2RuH8." Journal of Alloys and Compounds 645 (October 2015): S347—S352. http://dx.doi.org/10.1016/j.jallcom.2014.12.113.

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Dissertations / Theses on the topic "Transition metal hydrides – Synthesis"

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Fahlquist, Henrik. "Transition Metal Hydride Complexes and Hydrogenated Gallium Clusters : Synthesis and Structural Properties." Doctoral thesis, Stockholms universitet, Institutionen för material- och miljökemi (MMK), 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-89760.

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Synthesis and structural characterisation of metal hydrides in two important systems are presented. The first system presented is low valent cobalt and nickel complex hydrides with the compositions BaMg5Co2H10, RbMg5CoNiH10, SrMg2CoH7and Sr4Mg4Co3H19 featuring nickel with oxidation state of 0 and cobalt with oxidation state +I and -I. The second system presented is polyanionic gallium complex hydrides with the compositions RbGaH2, RbxK(1−x)GaH2 (0.5≤x≤1), CsxRb(8−x)Ga5H15 (0≤x≤8) and Cs10Ga9H25 featuring novel hydrogenous polyanionic gallium hydride clusters mimicking common hydrocarbons. The syntheses of the compounds were performed at elevated temperatures and at moderate hydrogen pressures (50-100 bar). The structural investigations were mainly done by X-ray powder diffraction (XRPD) and neutron powder diffraction (NPD). The metal-hydrogen bond was investigated by vibrational spectroscopy using Fourier Transform IR-spectroscopy (FTIR) and Inelastic Neutron Scattering (INS).By subtle changes in the compositions of the hydrides it was possible to induce major changes in band gaps, oxidation states and structures.

At the time for the doctoral defence the following papers were unpublished and had a status as follows: Paper 1: Manuscript; Paper 2: Accepted; Paper 5: Manuscript

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Mellows, Heather. "Synthesis and properties of two fold symmetric ruthenium and rhodium dihydrogen-hydride complexes /." Thesis, Connect to this title online; UW restricted, 2000. http://hdl.handle.net/1773/8598.

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Riddlestone, Ian Martin. "Synthesis and reactivity of transition metal-group 13 complexes." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:f253a2a5-cc6e-4978-86d9-5f3064dadc1b.

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The synthesis and reactivity of a number of mixed transition metal-aluminium and σ-alane complexes are detailed in this thesis. Chapter III reports on the formation and structural characterisation of N,N'-chelated aluminium dihalide precursors featuring amidinate and guanidinate substituents. These precursors of the type RC(R'N)2AlX2 (R = iPr2N or Ph; R' = Cy or iPr or Dipp; X = hal), readily react with Na[CpFe(CO)2] via salt elimination to form the corresponding mixed iron-aluminium complexes CpFe(CO)2[(X)Al(NR')2CR] which have been characterised both spectroscopically and by X-ray diffraction. The reactivity of the novel mixed aluminium-iron complexes towards halide abstraction agents has been investigated and a propensity for augmented coordination at the aluminium centre observed. Furthermore, complementary syntheses of the methyl substituted complex CpFe(CO)2[(Me)Al(NCy)2CNiPr2] have been developed. This can be achieved either via the reaction between the related chloride complex and MeLi, or from the reaction between iPr2C(CyN)2Al(Me)Cl and Na[CpFe(CO)2]. The research detailed in Chapter IV builds on the previous chapter and is focussed on the use of more sterically demanding substituents at both aluminium and transition metal, as well as more electron rich transition metal fragments. The transition metal anions Na[Cp*Fe(CO)2] and Na[CpSiFe(CO)(PPh3)] react with the aluminium precursors forming related mixed iron-aluminium complexes which have been structurally characterised. The Dipp2NacNacAlCl2 precursor has been shown to undergo reaction with both Na[CpFe(CO)2] and Na[Cp*Fe(CO)2]. The halide abstraction chemistry of the latter utilising both Lewis acid and salt metathesis based abstraction approaches has been investigated. The dehydrohalogenation chemistry of the Dipp2NacNacAlCl2 precursor was investigated and the ligand activated products of reactions with both alkyl lithium and alkyl potassium reagents characterised. Chapter V reports the extension of salt metathesis for the formation of an Al-H-Mn interaction, and the product has been fully characterised. In addition, the coordination of Al-H bonds from a number of alane precursors to in situ generated 16-electron fragments has allowed the structural characterisation of a number of novel σ-alane complexes. The incorporation of the transition metal fragments [Cp'Mn(CO)2] and [W(CO)5] permit comparison to archetypal borane and silane σ-complexes. Quantum chemical calculations suggest that the alane ligand has a binding energy close to that of dihydrogen but significantly less than that of CO, consistent with a predominant σ-donor role of the Al-H bond. The formation and structural characterisation of the κ2-complexes (OC)4M[κ2-H2AlDipp2NacNac] (M = Cr, Mo or W) define an unprecedented binding motif for the alane ligand. In the cases of chromium and molybdenum the κ2-complexes can be prepared either photolytically or via alkene displacement from the corresponding (OC)4M(cod) reagent. In the case of tungsten the alkene displacement route yields the desired product, but only under more forcing conditions. Spectroscopic characterisation of the related κ1-complex (OC)5Cr[κ1-H2AlDipp2NacNac], which readily forms the κ2-complex in solution without photolysis, has enabled the kinetics of chelate ring closure to be investigated. This analysis further characterises the formation of the unprecedented κ2-binding motif for the alane ligand.
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Hayward, Michael Andrew. "The synthesis and characterisation of some novel reduced transition metal oxides." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326022.

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Oldham, Warren James. "Synthesis and NMR properties of dihydrogen-hydride complexes of rhodium and iridium /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/8505.

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Bouilly, Guillaume Jacques. "Synthesis and characterization of transition metal oxides and oxyhydrides using epitaxial thin films deposition." 京都大学 (Kyoto University), 2015. http://hdl.handle.net/2433/200450.

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Bai, Guangcai. "New methods for the syntheses of amido, imido, nitrido and dinitrogen metal complexes and organometallic hydrides and oxides." Doctoral thesis, [S.l.] : [s.n.], 2001. http://webdoc.sub.gwdg.de/diss/2002/bai/bai.pdf.

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White, James P. "Synthesis and characterization of divalent lanthanide (Ln²[superscript plus] = Sm, Eu, Yb) coordination complexes with boron hydride and transition metal carbonyl anions : the formation of metallic films and metal borides from complex precursors /." The Ohio State University, 1990. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487681788254429.

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Sivakumar, V. "Influence Of The Bite Angles Of Chelating Diphosphine Ligands In The Chemistry Of Ruthenium Hydride And Dihydrogen Complexes." Thesis, Indian Institute of Science, 2006. http://hdl.handle.net/2005/293.

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The bite angle of a diphosphine ligand plays an important role in determining the reactivity of a transition metal complex. The coordinated dihydrogen on a transition metal center can be activated toward homolysis or heterolysis depending upon the nature of the metal center and the ancillary ligand environment. The present work deals with our investigations on the effect of the bite angle of the chelating diphosphine ligands in the chemistry of certain ruthenium hydride and dihydrogen complexes. Protonation of the ds-[Ru(H)2(dppm)(PPh3)2] (dppm = Ph2PCH2PPh2) using HBF4-Et2O resulted in the dihydrogen/hydride complex trans-(Formula). This species shows dynamic exchange of the H-atom between the dihydrogen and the hydride ligands. The H-atom site exchange was studied by NMR spectroscopy. Attempts to prepare the ruthenium dihydride complexes, cis-[Ru(H)2(dppe)(PPh3)2] (dppe = Ph2PCH2CH2PPh2) and cw-[Ru(H)2(dppp)(PPh3)2] (dppp = Ph2PCH2CH2CH2PPh2) with larger bite-angled diphosphines dppe and dppp were unsuccessful. Earlier work in our group on the effect of trans nitrile ligands in a series of complexes of the type (Formula)howed that the properties of the bound H2 are almost invariant with a change in the R group of the nitrile. hi an effort to compare those results with analogous ruthenium complexes bearing smaller bite-angled diphosphine, dppm, we synthesized and characterized a series of complexes of the type (Formula). We found that the properties of the bound H2 were once again invariant with a change in the R group of the nitrile. In an effort to compare the effect of having two diphosphine ligands of different bite angles with systems containing symmetrical diphosphine ligands reported by our group,3 we synthesized a series of complexes of the type (Formula). These complexes exhibit hybrid properties in comparison to systems with symmetrical diphosphine ligands in terms of spectroscopic features and chemical reactivity. Thus, the bite angle of the diphosphine ligand has a definite influence on the properties of the bound H2 ligand.
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Ekström, Jesper. "Transition metal hydrides : biomimetic studies and catalytic applications /." Stockholm : Department of Organic Chemistry, Stockholm University, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-7187.

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Books on the topic "Transition metal hydrides – Synthesis"

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International Symposium on the Properties and Applications of Metal Hydrides (1986 Maubuisson, France). Metal hydrides, 1986: Proceedings of the International Symposium on the Properties and Applications of Metal Hydrides V, Maubuisson, France, May 25-30, 1986. Edited by Percheron-Guegan A and Gupta M. Lausanne: Elsevier Sequoia, 1987.

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McQuillin, F. J. Transition metal organometallics for organic synthesis. Cambridge: Cambridge University Press, 1991.

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Wu, Xiao-Feng, and Matthias Beller, eds. Transition Metal Catalyzed Carbonylative Synthesis of Heterocycles. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-24963-6.

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Brandsma, L. Application of transition metal catalysts in organic synthesis. Berlin: Springer, 1998.

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Brandsma, Lambert. Application of transition metal catalysts in organic synthesis. Berlin: Springer, 1998.

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Brandsma, L., H. D. Verkruijsse, and S. F. Vasilevsky. Application of Transition Metal Catalysts in Organic Synthesis. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60328-0.

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1940-, Vasilevsky S. F., and Verkruijsse H. D, eds. Application of transition metal catalysts in organic synthesis. Berlin: Springer, 1999.

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J. T. G. Taylor Gomes. The synthesis of asymmetric ligands for transition metal catalysis. Manchester: UMIST, 1995.

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Obuzor, Gloria U. Synthesis of new cyclopentadienyl and indenyl transition metal complexes. Manchester: UMIST, 1998.

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Kazmaier, Uli. Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2012.

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Book chapters on the topic "Transition metal hydrides – Synthesis"

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Brunner, Henri. "Optically Active Transition Metal Compounds Containing Chiral Transition Metal Atoms." In Chemical Synthesis, 91–111. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0255-8_4.

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Miller, Thomas M., Amy E. Stevens Miller, and John F. Paulson. "Dissociative Electron Attachment to Transition-Metal Hydrides." In Dissociative Recombination, 273–74. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2976-7_28.

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Beletskaya, I. P., and A. V. Cheprakov. "Aqueous transition-metal catalysis." In Organic Synthesis in Water, 141–222. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4950-1_5.

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Pedneault, Sylvain, L. Roué, and Jacques Huot. "Synthesis of Metal Hydrides by Cold Rolling." In Metastable and Nanostructured Materials III, 33–38. Stafa: Trans Tech Publications Ltd., 2008. http://dx.doi.org/10.4028/0-87849-474-x.33.

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Suginome, Michinori, and Yoshihiko Ito. "Transition Metal-Mediated Polymerization of Isocyanides." In Polymer Synthesis, 77–136. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b95531.

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Brunner, Henri. "Enantioselective Catalysis with Transition Metal Complexes." In Chemical Synthesis, 175–90. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0255-8_7.

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Rauchfuss, Thomas B. "Synthesis of Transition Metal Dithiolenes." In Progress in Inorganic Chemistry, 1–54. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471471933.ch1.

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Genet, J. P. "Transition metal catalysts for asymmetric reduction." In Advanced Asymmetric Synthesis, 146–80. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-007-0797-9_8.

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Beller, Matthias, and Xiao-Feng Wu. "Applications in Total Synthesis." In Transition Metal Catalyzed Carbonylation Reactions, 187–213. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-39016-6_10.

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Kandalova, N. V., S. P. Sirotinkin, and V. N. Verbetsky. "Synthesis and Properties of Mg2EuH5.5." In Hydrogen Materials Science and Chemistry of Metal Hydrides, 125–30. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0558-6_14.

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Conference papers on the topic "Transition metal hydrides – Synthesis"

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Sharma, Ramesh, Seema Shukla, Shalini Dwivedi, and Yamini Sharma. "Ab-initio study of transition metal hydrides." In SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872870.

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Shrestha, Santosh, Simon Chung, Neeti Gupta, Pei Wang, Xiaoming Wen, and Gavin Conibeer. "Potential of transition metal nitrides and hydrides as hot carrier solar cell absorbers." In 2015 IEEE 42nd Photovoltaic Specialists Conference (PVSC). IEEE, 2015. http://dx.doi.org/10.1109/pvsc.2015.7356109.

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LLAMAS-JANSA, I., C. RONGEAT, S. DOPPIU, and O. GUTFLEISCH. "SYNTHESIS AND MODIFICATION OF LIGHT METAL AND COMPLEX HYDRIDES BY HIGH-ENERGY BALL MILLING." In Proceedings of the International Symposium. WORLD SCIENTIFIC, 2009. http://dx.doi.org/10.1142/9789812838025_0013.

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Merchan-Merchan, W., A. V. Saveliev, and Aaron Taylor. "Flame Synthesis of Nanostructured Transition Metal Oxides." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-68987.

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Various transition metal oxide nanostructures are synthesized using a novel probe-flame interaction method. An opposed flow flame of methane and oxygen enriched air provides a high-temperature reacting environment forming various metal oxide structures directly on the surface of pure metal probes. The unique thermal profile and chemical composition of the generated flame tends to convert almost pure bulk (99.9%) metallic materials into 1-D and 3-D structures of different chemical compositions and unique morphologies. The synthesized molybdenum, tungsten, and iron oxide structures exhibit unique morphological characteristics. The application of Mo probes results in the formation of micron size hollow and non-hollow Mo-oxide channels and elongated structures with cylindrical shapes. The use of W probes results in the synthesis of 1-D carbon-oxide nanowires, 3-D structures with rectangular shapes, and thin oxide plates with large surface areas. The formation of elongated iron-oxide nanorods is observed on iron probes. The iron nanorods’ diameters range from ten nanometers to one hundred nanometers with lengths of a few micrometers. Flame position, probe diameter, and flame exposure time tend to play an important role for material shape and selectivity.
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Pietschnig, Rudolf, Carmen Moser, Stefan Spirk, and Sven Schäfer. "Synthesis and Structure of Transition Metal Bisalkinylselenolato Complexes." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01518.

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Abbas, Omar Adnan, Adam Henry Lewis, Nikos Aspiotis, Chung-Che Huang, Ioannis Zeimpekis, Dan Hewak, Pier Sazio, and Sakellaris Mailis. "Direct Laser Synthesis of Two-Dimensional Transition Metal Dichalcogenides." In 2019 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC). IEEE, 2019. http://dx.doi.org/10.1109/cleoe-eqec.2019.8871667.

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Ashok, Anchu, Anchu Ashok, Anand Kumar, and Yussuf Olasunkanmi Kuti. "Synthesis Of Transition Metal Nanoparticles Using Combustion Based Techniques." In Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2014. http://dx.doi.org/10.5339/qfarc.2014.eepp1173.

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Wesch, W., O. Picht, M. Steinert, A. Undisz, M. Rettenmayr, U. Kaiser, J. Biskupek, N. A. Sobolev, Floyd D. McDaniel, and Barney L. Doyle. "Ion Beam Synthesis of Transition Metal Nanoclusters in Silicon." In APPLICATION OF ACCELERATORS IN RESEARCH AND INDUSTRY: Twentieth International Conference. AIP, 2009. http://dx.doi.org/10.1063/1.3120054.

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Aleksandrova, O. A., D. S. Mazing, L. B. Matyushkin, S. F. Musikhin, A. V. Nikiforova, V. A. Moshnikov, and V. Barzda. "Synthesis of transition metal doped zinc selenide nanoparticles for bioimaging." In 2015 Photonics North. IEEE, 2015. http://dx.doi.org/10.1109/pn.2015.7292477.

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Ullah, Ruh, and Joydeep Dutta. "Synthesis and Optical Properties of Transition Metal Doped ZnO Nanoparticles." In 2007 International Conference on Emerging Technologies (ICET). IEEE, 2007. http://dx.doi.org/10.1109/icet.2007.4516363.

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Reports on the topic "Transition metal hydrides – Synthesis"

1

Fox, K. SYNTHESIS OF METAL HYDRIDES BY MECHANICAL ALLOYING IN AN ATTRITOR MILL: FY07 STATUS REPORT. Office of Scientific and Technical Information (OSTI), November 2007. http://dx.doi.org/10.2172/921679.

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2

Fox, K. SYNTHESIS OF METAL HYDRIDES BY MECHANICAL ALLOYING IN AN ATTRITOR MILL: FY06 STATUS REPORT. Office of Scientific and Technical Information (OSTI), November 2006. http://dx.doi.org/10.2172/922281.

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3

Casteel, Jr., William Jack. The synthesis and structural characterization of novel transition metal fluorides. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/10190395.

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4

Casteel, W. J. Jr. The synthesis and structural characterization of novel transition metal fluorides. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/7017272.

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5

Browning, Robert. Synthesis and Characterization of the 2-Dimensional Transition Metal Dichalcogenides. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.5367.

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6

Cadieu, F. J. Direct Synthesis and Optimization of Rare Earth Transition Metal Permanent Magnet Systems. Fort Belvoir, VA: Defense Technical Information Center, September 1986. http://dx.doi.org/10.21236/ada172955.

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7

Reinig, Regina Rose. Synthesis and reactivity of paramagnetic late transition metal complexes supported by tris(oxazolinyl)phenylborate. Office of Scientific and Technical Information (OSTI), May 2018. http://dx.doi.org/10.2172/1505192.

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8

Limbach, H. H., S. Ulrich, G. Buntkowsky, S. Sabo-Etienne, B. Chaudret, G. J. Kubas, and J. Eckert. A unified view of coherent and incoherent dihydrogen exchange in transition metal hydrides by nuclear resonance and inelastic neutron scattering. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/206446.

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9

Das, Supriyo. Synthesis and structural, magnetic, thermal, and transport properties of several transition metal oxides and aresnides. Office of Scientific and Technical Information (OSTI), January 2010. http://dx.doi.org/10.2172/985308.

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10

Derakhshan, Shahab, and Yohannes Abate. Near-Field Nanoscopy of Metal-Insulator Phase Transitions Towards Synthesis of Novel Correlated Transition Metal Oxides and Their Interaction with Plasmon Resonances. Fort Belvoir, VA: Defense Technical Information Center, January 2016. http://dx.doi.org/10.21236/ad1007386.

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