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Rücktitelbild: Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair (Angew. Chem. 10/2019).
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3262, doi. 10.1002/ange.201901616
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Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair.
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 3134, doi. 10.1002/ange.201810945
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Roles of Solvent in the Catalytic Hydrogen Release from Liquid Organic Hydrogen Carriers: Chemical, Thermodynamical and Technological Aspects.
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- Topics in Catalysis, 2024, v. 67, n. 13/14, p. 892, doi. 10.1007/s11244-024-01950-8
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Hydrogen Energy.
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- ChemPhysChem, 2019, v. 20, n. 10, p. 1157, doi. 10.1002/cphc.201900429
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Leveraging Curvature on N‐Doped Carbon Materials for Hydrogen Storage.
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- Small, 2024, v. 20, n. 25, p. 1, doi. 10.1002/smll.202310162
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The Ethanol–Ethyl Acetate System as a Biogenic Hydrogen Carrier.
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- Energy Technology, 2023, v. 11, n. 1, p. 1, doi. 10.1002/ente.202200892
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Back Cover: Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair (Angew. Chem. Int. Ed. 10/2019).
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- Angewandte Chemie International Edition, 2019, v. 58, n. 10, p. 3228, doi. 10.1002/anie.201901616
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Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 10, p. 3102, doi. 10.1002/anie.201810945
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Nanoscaffold Mediates Hydrogen Release and the Reactivity of Ammonia BoraneThis research was performed in part at the Interfacial and Nano Science Facility in the William R. Wiley Environmental Molecular Sciences Laboratory, a national scientific user facility sponsored by the Office of Biological and Environmental Research of the US Department of Energy and located at the Pacific Northwest National Laboratory (PNNL). Pacific Northwest is operated for the Department of Energy by Battelle. The authors wish to acknowledge support from the Laboratory Directed Research and Development Program at the PNNL and the Nano Science & Technology Initiative. T.A. thanks D. Thorn (LANL) and D. Schubert (US Borax) for helpful discussions.
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- Angewandte Chemie, 2005, v. 117, n. 23, p. 3644, doi. 10.1002/ange.200462602
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Nanoscaffold Mediates Hydrogen Release and the Reactivity of Ammonia BoraneThis research was performed in part at the Interfacial and Nano Science Facility in the William R. Wiley Environmental Molecular Sciences Laboratory, a national scientific user facility sponsored by the Office of Biological and Environmental Research of the US Department of Energy and located at the Pacific Northwest National Laboratory (PNNL). Pacific Northwest is operated for the Department of Energy by Battelle. The authors wish to acknowledge support from the Laboratory Directed Research and Development Program at the PNNL and the Nano Science & Technology Initiative. T.A. thanks D. Thorn (LANL) and D. Schubert (US Borax) for helpful discussions.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 23, p. 3578, doi. 10.1002/anie.200462602
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- Article
Heterolysis of H<sub>2</sub> Across a Classical Lewis Pair, 2,6-Lutidine⋅BCl<sub>3</sub>: Synthesis, Characterization, and Mechanism.
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- Chemistry - A European Journal, 2015, v. 21, n. 44, p. 15713, doi. 10.1002/chem.201501899
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Growth of Crystalline Polyaminoborane through Catalytic Dehydrogenation of Ammonia Borane on FeB Nanoalloy.
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- Chemistry - A European Journal, 2010, v. 16, n. 43, p. 12814, doi. 10.1002/chem.201001844
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Effects of Glymes on the Distribution of Mg(B 10 H 10) and Mg(B 12 H 12) from the Thermolysis of Mg(BH 4) 2.
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- Inorganics, 2021, v. 9, n. 6, p. 41, doi. 10.3390/inorganics9060041
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Lewis Base Complexes of Magnesium Borohydride: Enhanced Kinetics and Product Selectivity upon Hydrogen Release.
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- Inorganics, 2017, v. 5, n. 4, p. 89, doi. 10.3390/inorganics5040089
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Mechanistic Investigation on the Formation and Dehydrogenation of Calcium Amidoborane Ammoniate.
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- ChemSusChem, 2012, v. 5, n. 5, p. 927, doi. 10.1002/cssc.201100523
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In Situ Multinuclear NMR Spectroscopic Studies of the Thermal Decomposition of Ammonia Borane in Solution.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 39, p. 7493, doi. 10.1002/anie.200802100
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THE PHOTOCHEMISTRY OF 3-NITROBENZOYL AND 4-NITROBENZOYL AZIDES: POSSIBLE REAGENTS FOR PHOTOAFFINITY LABELING.
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- Photochemistry & Photobiology, 1988, v. 47, n. 4, p. 497, doi. 10.1111/j.1751-1097.1988.tb08837.x
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