Journal articles: 'Sodium hydride'

1

Verma, Abha. "Sodium Hydride." Synlett 2010, no. 15 (August 30, 2010): 2361–62. http://dx.doi.org/10.1055/s-0030-1258067.

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Verma, Abha. "Sodium Hydride." Synlett 2010, no. 15 (September 2010): e8-e8. http://dx.doi.org/10.1055/s-0030-1258558.

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Konashi, Kenji, Kunihiro Itoh, Tsugio Yokoyama, and Michio Yamawaki. "Utilization Research and Development of Hydride Materials in Fast Reactors." Advances in Science and Technology 94 (October 2014): 23–31. http://dx.doi.org/10.4028/www.scientific.net/ast.94.23.

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Metal hydrides have high hydrogen atom density, which is equivalent to that of liquid water. An application of the hafnium hydride has been investigated as a neutron absorber in the Fast Breeder Reactors (FBRs). Fast neutrons are efficiently moderated by hydrogen in Hf hydrides and are absorbed by Hf. Since three isotopes of Hf have large cross sections, increase in the life of control rod is considered by Hf hydride. Results of design study of the core with Hf hydride control rods shows that the long lived hafnium hydride control rod is feasible in the large sodium-cooled FBR. Results of irradiation test conducted in BOR-60 has demonstrated the integrity of the capsules during irradiation. Na bonded capsule has an advantage in confinement effect of hydrogen compared with He bonded one. An application of hydride technique to transmutation target of MA was also discussed. MA hydride target is able to enhance the transmutation rate in FBR.

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Konashi, Kenji, and Michio Yamawaki. "Utilization of Hydride Materials in Nuclear Reactors." Advances in Science and Technology 73 (October 2010): 51–58. http://dx.doi.org/10.4028/www.scientific.net/ast.73.51.

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Metal hydrides have high hydrogen atom density, which is equivalent to that of liquid water. Fast neutrons are efficiently moderated by hydrogen in metal hydrides. Metal hydrides have been studied for their potential application as nuclear materials in fast reactors (FRs). Two types of the utilizations of metal hydride in FRs are discussed in this paper. One is the utilization for transmutation target of long-lived nuclear wastes. Hydride fuel containing 237Np, 241Am and 243Am has been studied as a candidate transmutation target to reduce the radioactivity of long-lived nuclides included in reprocessed nuclear wastes. An application of the hafnium hydride has been investigated as neutron absorber in FRs. The core design has been performed to examine its characteristics and to evaluate the cost reduction effect. Demonstration of fabrication of hydride pin has been done with hydride pellets and stainless steel cladding. Coating technique of inner cladding surface has been also developed to reduce the permeation of hydrogen through stainless steel cladding. Physical and chemical properties of the pellet have been measured for designing the hydride pin. The integrity of the pellets at high temperature has been tested and their compatibility with sodium has also been tested. Irradiation test of hydrides has been performed in the fast experimental reactor, JOYO, at Japan Atomic Energy Association (JAEA).

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Too, Pei Chui, Guo Hao Chan, Ya Lin Tnay, Hajime Hirao, and Shunsuke Chiba. "Hydride Reduction by a Sodium Hydride-Iodide Composite." Angewandte Chemie International Edition 55, no. 11 (February 16, 2016): 3719–23. http://dx.doi.org/10.1002/anie.201600305.

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Too, Pei Chui, Guo Hao Chan, Ya Lin Tnay, Hajime Hirao, and Shunsuke Chiba. "Hydride Reduction by a Sodium Hydride-Iodide Composite." Angewandte Chemie 128, no. 11 (February 17, 2016): 3783–87. http://dx.doi.org/10.1002/ange.201600305.

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7

Dixon, David A., James L. Gole, and Andrew Komornicki. "Absolute proton affinities of lithium dimer, sodium dimer, lithium hydride, and sodium hydride." Journal of Physical Chemistry 92, no. 8 (April 1988): 2134–36. http://dx.doi.org/10.1021/j100319a010.

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8

Mahmoud, Mahmoud R., Manal M. El-Shahawi, Eman A. A. El-Bordany, and Fatma S. M. Abu El-Azm. "Synthesis and reactions of indeno[1,2-c]chromene-6,11-dione derivatives." Journal of Chemical Research 2008, no. 11 (November 2008): 609–12. http://dx.doi.org/10.3184/030823408x360364373.

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Indeno[1,2-c]chromene-6,11-dione was prepared using the readily obtainable starting materials via the condensation of dimethyl homophthalate with 2,6-dichlorobenzaldehyde in the presence of sodium hydride in dry benzene followed by saponification and cyclisation with concentrated sulfuric acid at 0°C. The tendency of indeno[1,2-c]chromene-6,11-dione for undergoing nucleophilic addition has been tested by reaction with nitrogen nucleophiles such as hydrazine hydrate, hydroxylamine hydrochloride, ethyl carbazate, cyanoacetic acid hydrazide, thiosemicarbazide and 4-methylbenzenesulfonohydrazide. The IR, 1H NMR, 13C NMR and mass spectra of the synthesised compounds are discussed.

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9

Maki, Arthur G., and Wm Bruce Olson. "Infrared spectrum of sodium hydride." Journal of Chemical Physics 90, no. 12 (June 15, 1989): 6887–92. http://dx.doi.org/10.1063/1.456263.

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10

Werner, Thomas, and Juliane Koch. "Sodium Hydride Catalyzed Tishchenko Reaction." European Journal of Organic Chemistry 2010, no. 36 (November 17, 2010): 6904–7. http://dx.doi.org/10.1002/ejoc.201001294.

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11

Rathi, Akshat. "Sodium Bis(methoxyethoxy)aluminium Hydride." Synlett 2010, no. 07 (March 23, 2010): 1140–41. http://dx.doi.org/10.1055/s-0029-1219578.

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12

Bogdanovic, Borislav, Michael Felderhoff, and Guido Streukens. "Hydrogen storage in complex metal hydrides." Journal of the Serbian Chemical Society 74, no. 2 (2009): 183–96. http://dx.doi.org/10.2298/jsc0902183b.

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Complex metal hydrides such as sodium aluminohydride (NaAlH4) and sodium borohydride (NaBH4) are solid-state hydrogen-storage materials with high hydrogen capacities. They can be used in combination with fuel cells as a hydrogen source thus enabling longer operation times compared with classical metal hydrides. The most important point for a wide application of these materials is the reversibility under moderate technical conditions. At present, only NaAlH4 has favorable thermodynamic properties and can be employed as a thermally reversible means of hydrogen storage. By contrast, NaBH4 is a typical non-reversible complex metal hydride; it reacts with water to produce hydrogen.

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13

Wang, Jun-qin, Jian-feng Gao, Zhi-gang Wu, Guo-li Ou, and Yu Wang. "Synthesis of Renewable Energy Materials, Sodium Aluminum Hydride by Grignard Reagent of Al." Journal of Nanomaterials 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/296486.

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The research on hydrogen generation and application has attracted widespread attention around the world. This paper is to demonstrate that sodium aluminum hydride can be synthesized under simple and mild reaction condition. Being activated through organics, aluminum powder reacts with hydrogen and sodium hydride to produce sodium aluminum hydride under atmospheric pressure. The properties and composition of the sample were characterized by FTIR, XRD, SEM, and so forth. The results showed that the product through this synthesis method is sodium aluminum hydride, and it has higher purity, perfect crystal character, better stability, and good hydrogen storage property. The reaction mechanism is also discussed in detail.

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14

HASHIMOTO, Shinichi. "Lithium aluminum hydride and Sodium aluminum hydride(LiAlH4 & NaAlH4)." Journal of Synthetic Organic Chemistry, Japan 52, no. 7 (1994): 616–17. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.616.

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15

Stasch, Andreas. "A pyrazolate-stabilized sodium hydride complex." Chemical Communications 51, no. 24 (2015): 5056–58. http://dx.doi.org/10.1039/c5cc00996k.

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16

Sawicka, Agnieszka, Piotr Skurski, and Jack Simons. "Inverse Sodium Hydride: A Theoretical Study." Journal of the American Chemical Society 125, no. 13 (April 2003): 3954–58. http://dx.doi.org/10.1021/ja021136v.

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17

Leopold, K. R., L. R. Zink, K. M. Evenson, and D. A. Jennings. "Far-infrared spectrum of sodium hydride." Journal of Molecular Spectroscopy 122, no. 1 (March 1987): 150–56. http://dx.doi.org/10.1016/0022-2852(87)90225-6.

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18

Sun, Tai, Kateryna Peinecke, Robert Urbanczyk, and Michael Felderhoff. "Influence of Synthesis Gas Components on Hydrogen Storage Properties of Sodium Aluminum Hexahydride." Hydrogen 2, no. 1 (February 26, 2021): 147–59. http://dx.doi.org/10.3390/hydrogen2010009.

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A systematic study of different ratios of CO, CO2, N2 gas components on the hydrogen storage properties of the Na3AlH6 complex hydride with 4 mol% TiCl3, 8 mol% aluminum and 8 mol% activated carbon is presented in this paper. The different concentrations of CO and CO2 in H2 and CO, CO2, N2 in H2 mixture were investigated. Both CO and CO2 gas react with the complex hydride forming Al oxy-compounds, NaOH and Na2CO3 that consequently cause serious decline in hydrogen storage capacity. These reactions lead to irreversible damage of complex hydride under the current experimental condition. Thus, after 10 cycles with 0.1 vol % CO + 99.9 vol %H2 and 1 vol % CO + 99 vol %H2, the dehydrogenation storage capacity of the composite material decreased by 17.2% and 57.3%, respectively. In the case of investigation of 10 cycles with 1 vol % CO2 + 99 vol % H2 gas mixture, the capacity degradation was 53.5%. After 2 cycles with 10 vol % CO +90 vol % H2, full degradation was observed, whereas after 6 cycles with 10 vol % CO2 + 90 vol % H2, degradation of 86.8% was measured. While testing with the gas mixture of 1.5 vol % CO + 10 vol % CO2 + 27 vol % H2 + 61.5 vol % N2, the degradation of 94% after 6 cycles was shown. According to these results, it must be concluded that complex aluminum hydrides cannot be used for the absorption of hydrogen from syngas mixtures without thorough purification.

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19

Lin, Kuen-Song, Yao-Jen Mai, Su-Wei Chiu, Jing-How Yang, and Sammy L. I. Chan. "Synthesis and Characterization of Metal Hydride/Carbon Aerogel Composites for Hydrogen Storage." Journal of Nanomaterials 2012 (2012): 1–9. http://dx.doi.org/10.1155/2012/201584.

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Two materials currently of interest for onboard lightweight hydrogen storage applications are sodium aluminum hydride (NaAlH4), a complex metal hydride, and carbon aerogels (CAs), a light porous material connected by several spherical nanoparticles. The objectives of the present work have been to investigate the synthesis, characterization, and hydrogenation behavior of Pd-, Ti- or Fe-doped CAs, NaAlH4, and MgH2nanocomposites. The diameters of Pd nanoparticles onto CA’s surface and BET surface area of CAs were 3–10 nm and 700–900 m2g−1, respectively. The H2storage capacity of metal hydrides has been studied using high-pressure TGA microbalance and they were 4.0, 2.7, 2.1, and 1.2 wt% for MgH2-FeTi-CAs, MgH2-FeTi, CAs-Pd, and 8 mol% Ti-doped NaAlH4, respectively, at room temperature. Carbon aerogels with higher surface area and mesoporous structures facilitated hydrogen diffusion and adsorption, which accounted for its extraordinary hydrogen storage phenomenon. The hydrogen adsorption abilities of CAs notably increased after inclusion of metal hydrides by the “hydrogen spillover” mechanisms.

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20

Jacoby, Denis, Carlo Floriani, Angiola Chiesi-Villa, and Corrado Rizzoli. "Zirconium meso-octaethylporphyrinogen as a carrier for sodium hydride in toluene: zirconium-sodium bimetallic hydride and alkyls." Journal of the American Chemical Society 115, no. 9 (May 1993): 3595–602. http://dx.doi.org/10.1021/ja00062a024.

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21

Včelák, Jaroslav, Anna Friesová, Roman Řeřicha, and Jiří Hetflejš. "Dehalogenation of Chlorobenzenes with Sodium Dihydridobis(2-methoxyethoxo)aluminate." Collection of Czechoslovak Chemical Communications 59, no. 6 (1994): 1368–83. http://dx.doi.org/10.1135/cccc19941368.

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The dehalogenation of a series of 9 mono- to pentachlorinated benzenes with the title hydride in toluene has been found to be first order in the substrate and half order in the hydride. The reactivities of the chlorobenzenes, expressed by rate constants for the first-step dehalogenation, increased with increasing number of chlorine atoms over three orders of magnitude. The rate data revealed the unexpected acceleration of benzene formation during exhaustive dehalogenation of the higher chlorinated benzenes. For comparison, dehalogenation of several isomeric dibromobenzenes and bromochlorobenzenes with the same hydride and the product distribution for the dehalogenation of some chlorobenzenes with LiAlH4 are also reported.

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22

Ong, Derek Yiren, Jia Hao Pang, and Shunsuke Chiba. "Synthetic Organic Reactions Mediated by Sodium Hydride." Journal of Synthetic Organic Chemistry, Japan 77, no. 11 (November 1, 2019): 1060–69. http://dx.doi.org/10.5059/yukigoseikyokaishi.77.1060.

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23

Chan, Guo. "Hydrodecyanation by a Sodium Hydride-Iodide Composite." Organic Syntheses 95 (2018): 240–55. http://dx.doi.org/10.15227/orgsyn.095.0240.

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24

Werner, Thomas, and Juliane Koch. "ChemInform Abstract: Sodium Hydride Catalyzed Tishchenko Reaction." ChemInform 42, no. 16 (March 24, 2011): no. http://dx.doi.org/10.1002/chin.201116077.

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25

Rajeev, Narasimhamurthy, Toreshettahally R. Swaroop, Ahmad I. Alrawashdeh, Shofiur Rahman, Abdullah Alodhayb, Seegehalli M. Anil, Kuppalli R. Kiran, et al. "The reaction of arylmethyl isocyanides and arylmethylamines with xanthate esters: a facile and unexpected synthesis of carbamothioates." Beilstein Journal of Organic Chemistry 16 (February 3, 2020): 159–67. http://dx.doi.org/10.3762/bjoc.16.18.

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An unexpected formation of carbamothioates by a sodium hydride-mediated reaction of arylmethyl isocyanides with xanthate esters in DMF is reported. The products thus obtained were compared with the carbamothioates obtained by the sodium hydride-mediated condensation of the corresponding benzylamines and xanthate esters in DMF. To account for these unexpected reactions, a mechanism is proposed in which the key steps are supported by quantum chemical calculations.

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26

Hong, Zonghan, Derek Yiren Ong, Subas Kumar Muduli, Pei Chui Too, Guo Hao Chan, Ya Lin Tnay, Shunsuke Chiba, Yusuke Nishiyama, Hajime Hirao, and Han Sen Soo. "Understanding the Origins of Nucleophilic Hydride Reactivity of a Sodium Hydride-Iodide Composite." Chemistry - A European Journal 22, no. 21 (April 1, 2016): 7108–14. http://dx.doi.org/10.1002/chem.201600340.

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27

Joo, Cheonik, Sunhae Kang, Sun Min Kim, Hogyu Han, and Jung Woon Yang. "Oxidation of benzoins to benzils using sodium hydride." Tetrahedron Letters 51, no. 46 (November 2010): 6006–7. http://dx.doi.org/10.1016/j.tetlet.2010.09.028.

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28

Reardon, Hazel, Natalia Mazur, and Duncan H. Gregory. "Facile synthesis of nanosized sodium magnesium hydride, NaMgH3." Progress in Natural Science: Materials International 23, no. 3 (June 2013): 343–50. http://dx.doi.org/10.1016/j.pnsc.2013.05.003.

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29

Czerwiński, Paweł J., and Bartłomiej Furman. "A Long-Sought Reactivity of a Sodium Hydride." Trends in Chemistry 2, no. 9 (September 2020): 782–84. http://dx.doi.org/10.1016/j.trechm.2020.07.001.

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30

Pavlenko, V. I., G. G. Bondarenko, O. V. Kuprieva, R. N. Yastrebinskii, and N. I. Cherkashina. "Modification of titanium hydride surface with sodium borosilicate." Inorganic Materials: Applied Research 5, no. 5 (September 2014): 494–97. http://dx.doi.org/10.1134/s207511331405013x.

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31

Enoki, Toshiaki, Noriaki Sakamoto, Keisuke Nakazawa, Kazuya Suzuki, Ko Sugihara, and Koji Kobayashi. "Electronic Structures of Sodium-Hydride-Graphite Intercalation Compounds." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 245, no. 1 (April 1994): 7–12. http://dx.doi.org/10.1080/10587259408051658.

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32

Prozorov, Tanya, Jun Wang, Armin D. Ebner, and James A. Ritter. "Sonochemical doping of Ti-catalyzed sodium aluminum hydride." Journal of Alloys and Compounds 419, no. 1-2 (August 2006): 162–71. http://dx.doi.org/10.1016/j.jallcom.2005.05.056.

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33

Magg, Ulrich, and Harold Jones. "The ground-state infrared spectrum of sodium hydride." Chemical Physics Letters 146, no. 5 (May 1988): 415–18. http://dx.doi.org/10.1016/0009-2614(88)87469-4.

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34

Baum, James Clayton, Kathleen Anne Durkin, Laura Precedo, Stacy Brian O'blenes, John Edward Goehl, Richard Francis Langler, Gerald Kendall MacCormack, and Lana Louise Smith. "Sulfonyl esters 3. The formation of sulfone-sulfonates in the reactions of aryl methanesulfonates with sodium hydride." Canadian Journal of Chemistry 69, no. 12 (December 1, 1991): 2127–35. http://dx.doi.org/10.1139/v91-307.

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Sodium hydride reductions of aryl methanesulfonates afford dimeric sulfone-sulfonate esters as well as products arising from SO bond rupture. SO bond rupture becomes more competitive as the LUMO energy of the sulfonate ester declines. Exploration of the chemistry of a sulfone-sulfonate ester revealed a complex novel reaction that resulted in the formation of, inter alia, a dichloromethanesulfonate ester and a trichloromethanesulfonate ester. The first successful approaches to the synthesis of the heretofore unknown trichloromethanesulfonates and dichloromethanesulfonates are reported. Key words: sodium hydride reductions, sulfenes, sulfone-sulfonate esters

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35

Pang, Jia Hao, Atsushi Kaga, and Shunsuke Chiba. "Nucleophilic amination of methoxypyridines by a sodium hydride–iodide composite." Chemical Communications 54, no. 73 (2018): 10324–27. http://dx.doi.org/10.1039/c8cc05979a.

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36

Bye, Ragnar. "Generation of selenium hydride from alkaline solutions: a new concept of the hydride generation-atomic absorption technique." Journal of Automatic Chemistry 11, no. 4 (1989): 156–58. http://dx.doi.org/10.1155/s1463924689000337.

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The use of hydride generation is often useful in environmental analysis. The normal acid sodium tetrahydroborate reaction provides exceptional sensitivity with continuous flow hydride generators. In some situations there are interferences which will mask the sensitivity. An alternative chemistry system is described here and is shown to offer similar sensitivity to that normally used. A commercial continuous flow analyser is used in this work.

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37

Dölling, Wolfgang, Helmut Hartungb, and Matthias Biedermann. "Reaktionen von 2-Methyl-1H-benzimidazol mit Schwefelkohlenstoff und Phenylisothiocyanat. Kristall- und Molekülstruktur von 1,1′ -Carbonothioyl-bis(2-methyl-1H-benzimidazol) und 2-Methyl-1-(ethoxycarbonylmethylthio-phenylimino)-1H-benzimidazol / Reactions of 2-Methyl-1 H-benzimidazole with Carbon Disulfide and Phenyl Isothiocyanate. Molecular and Crystal Structures of 1,1′-Carbonothioyl-bis(2-methyl-1 H-benzimidazole) and 2-Methyl-1-(ethoxycarbonylmethylthio-phenylimino)-1 H-benzimidazole." Zeitschrift für Naturforschung B 50, no. 5 (May 1, 1995): 837–43. http://dx.doi.org/10.1515/znb-1995-0525.

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Abstract 2-Methyl-1 H-benzimidazole 1 reacts in the presence of two equivalents of sodium hydride in dry DMSO with carbon disulfide to methyl 2-methylbenzimidazole-1-dithiocarboxylate 3 using methyl iodide as alkylating agent, whereas using 1,2-dibromoethane 1,1′-carbonothioyl bis(2-methyl-1 H-benzimidazole) 5 is formed. Compound 1 reacts with phenyl isothiocyanate in the presence of one equivalent of sodium hydride in dry DMF after alkylation to 2-methyl-1-( alkylthio-phenylimino)-1 H-benzimidazoles 6a, 6b. Reaction products 5 and 6b have been identified and structurally characterized by X-ray analysis.

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38

Lei, Jie Hong, Zheng Zhou Yan, Hao Duan, and Yun Juan Zhang. "Theoretical Study on Crystal Structure and Hydrogen Storage Properties of Sodium Hydride." Advanced Materials Research 287-290 (July 2011): 1348–51. http://dx.doi.org/10.4028/www.scientific.net/amr.287-290.1348.

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In this paper, the crystal structure and hydrogen storage properties of the sodium hydride at different x value (NaHxD1-x, NaHxT1-x, NaDxT1-x; x=0, 0.25, 0.5, 0.75, 1.0) are investigated by using density functional theory within the generalized gradient approximation (GGA). The calculated results of NaH (D, T) are in good agreement with the other theoretical results. It has been found that, densities decreased with the increase of x value, while lattice parameters stay constant. The hydrogen storage properties of sodium hydride were predicted. The density-value x (ρ-x) relationship, the variations of the hydrogen storage properties with different crystal structure were obtained systematically.

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39

Anderson, Kim A., and Brandon Isaacs. "Simultaneous Determination of Arsenic, Selenium, and Antimony in Environmental Samples by Hydride Generation for Inductively Coupled Plasma Atomic Emission Spectrometry." Journal of AOAC INTERNATIONAL 78, no. 4 (July 1, 1995): 1055–60. http://dx.doi.org/10.1093/jaoac/78.4.1055.

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Abstract Total arsenic, selenium, and antimony are determined simultaneously by inductively coupled plasma atomic emission spectrometry (ICP AES) with hydride vapor generation. A1 g wet, 0.25 g dry, or 10 mL water sample is digested by 1 of 2 methods in a 10 mL volumetric culture tube on a programmed heating block by heating with nitric acid and then boiling in a mixture of sulfuric and perchloric acids. For soils, a 0.25 g sample is digested in a 10 mL volumetric culture tube with hydrochloric acid. After digestion, the sample is treated with additional hydrochloric acid. Arsenic, selenium, and antimony are reduced to their hydrides by sodium borohydride in a simplified continuous- flow manifold. A standard pneumatic nebulizer separates the gaseous hydrides (AsH3, SeH2, and SbH3), which are then quantitated by ICP AES at 193.696,196.026, and 231.147 nm, respectively. The detection limits for As, Se, and Sb are 0.55,1.0, and 0.41 μg/L, respectively. Recoveries from 10 matrixes are 65 to 109%; recovery ranges for As, Se, and Sb are 81–109,87–108, and 65–123%, respectively. The method demonstrates good accuracy and precision for environmental samples and is especially suited for analysis of small samples. It requires no additional apparatus for hydride generation or sample introduction.

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40

Akkus, Meryem Sena, and Goksel Ozkan. "Investigation of Synthesis of Sodium Aminodiborane in One Step and Its Reaction Kinetics." Molekul 15, no. 3 (November 27, 2020): 219. http://dx.doi.org/10.20884/1.jm.2020.15.3.681.

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In this study, sodium aminodiborane (NaNH2(BH3)2) synthesis was carried out in a constant volume batch reactor with a single feed at various temperatures and inlet molar ratios. It was synthesized, ammonia borane and sodium hydride as precursors, by a wet chemical reaction method using tetrahydrofuran which is a solvent under atmospheric pressure. These experiments were carried out at varied temperature ranges from 0 °C to 24 °C, and varied inlet molar ratios (AB/NaH) from 0.75 to 1.25. Sodium amidoborane is synthesized when the experiment is carried out in a stoichiometric ratio, but sodium aminodiborane is synthesized when the mole of ammonia borane is higher than the mole of sodium hydride. In order to characterize the products, FTIR, XRD, GC-MS/MS, and quantitative analysis techniques were utilized. In addition, sodium aminodiborane’s synthesis reaction kinetic was determined. r apparent = 0.8594 e ^ (- 4366 / RT) C AB ^ (0.8) C NaH ^ (0.2). The apparent activation energy, Ea, and frequency constant, k0, were calculated about 4366 J/mol and 0.8594 h-1, respectively

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41

Rakesh, K. P., A. B. Ramesha, C. S. Shantharam, K. Mantelingu, and N. Mallesha. "An unexpected reaction to methodology: an unprecedented approach to transamidation." RSC Advances 6, no. 110 (2016): 108315–18. http://dx.doi.org/10.1039/c6ra23374k.

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42

Yin-Heng, Fan, Liao Shi-Jian, and Yu Dao-Rong. "Thermal Stability and Chemical Reactivity of Nanometric Sodium Hydride." Acta Physico-Chimica Sinica 14, no. 12 (1998): 1057–60. http://dx.doi.org/10.3866/pku.whxb19981201.

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43

Shekhani, Mohammed Salehpp, Khalid Mohammed Khan, and Khalid Mahmood. "Reductive cleavage of t-butyldimethylsilyl ethers with sodium hydride." Tetrahedron Letters 29, no. 47 (1988): 6161–62. http://dx.doi.org/10.1016/s0040-4039(00)82294-7.

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44

Poupin, Lucas, Terry D. Humphries, Mark Paskevicius, and Craig E. Buckley. "A thermal energy storage prototype using sodium magnesium hydride." Sustainable Energy & Fuels 3, no. 4 (2019): 985–95. http://dx.doi.org/10.1039/c8se00596f.

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45

Ong, Derek Yiren, Ciputra Tejo, Kai Xu, Hajime Hirao, and Shunsuke Chiba. "Hydrodehalogenation of Haloarenes by a Sodium Hydride-Iodide Composite." Angewandte Chemie 129, no. 7 (January 10, 2017): 1866–70. http://dx.doi.org/10.1002/ange.201611495.

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46

Ong, Derek Yiren, Ciputra Tejo, Kai Xu, Hajime Hirao, and Shunsuke Chiba. "Hydrodehalogenation of Haloarenes by a Sodium Hydride-Iodide Composite." Angewandte Chemie International Edition 56, no. 7 (January 10, 2017): 1840–44. http://dx.doi.org/10.1002/anie.201611495.

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47

Kadir, K., and D. Noréus. "The Structure of a Sodium-substituted Palladium Hydride, NaPd3H2*." Zeitschrift für Physikalische Chemie 1, no. 1 (January 1992): 263–67. http://dx.doi.org/10.1524/zpch.1992.1.1.263.

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48

Kadir, K., and D. Noréus. "The Structure of a Sodium-substituted Palladium Hydride, NaPd3H2*." Zeitschrift für Physikalische Chemie 179, Part_1_2 (January 1993): 249–53. http://dx.doi.org/10.1524/zpch.1993.179.part_1_2.249.

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Sirota, D. S., and A. P. Pchel'nikov. "Electrochemical Behavior of Nickel Hydride in Sodium Hydroxide Solutions." Protection of Metals 40, no. 5 (September 2004): 441–46. http://dx.doi.org/10.1023/b:prom.0000043061.81634.d0.

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Pukazhselvan, D., M. Sterlin Leo Hudson, A. S. K. Sinha, and O. N. Srivastava. "Studies on metal oxide nanoparticles catalyzed sodium aluminum hydride." Energy 35, no. 12 (December 2010): 5037–42. http://dx.doi.org/10.1016/j.energy.2010.08.015.

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Journal articles on the topic 'Sodium hydride'

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