Search alternatives:
ng decrease » nn decrease (Expand Search), _ decrease (Expand Search), we decrease (Expand Search)
e decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
ng decrease » nn decrease (Expand Search), _ decrease (Expand Search), we decrease (Expand Search)
e decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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14161
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14162
Configuring Bonds between First-Row Transition Metals
Published 2015“…The potential of using metal–metal complexes for multielectron reduction of small-molecules is addressed by N<sub>2</sub> binding studies and a mechanistic study of a dicobalt catalyst in reductive silylation of N<sub>2</sub> to N(SiMe<sub>3</sub>)<sub>3</sub>. …”
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14163
Configuring Bonds between First-Row Transition Metals
Published 2015“…The potential of using metal–metal complexes for multielectron reduction of small-molecules is addressed by N<sub>2</sub> binding studies and a mechanistic study of a dicobalt catalyst in reductive silylation of N<sub>2</sub> to N(SiMe<sub>3</sub>)<sub>3</sub>. …”
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14164
Morphological Degradation of Oxygen Evolution Reaction-Electrocatalyzing Nickel Selenides at Industrially Relevant Current Densities
Published 2025“…Morphological degradation of the catalyst material was only observed at current densities exceeding 1 A cm<sup>–2</sup> but not for smaller ones. Using X-ray absorption, X-ray photoemission spectroscopy, and X-ray diffraction, we confirmed that the degradation was accompanied by the literature-known transformation of nanoparticulate Ni<sub>3</sub>Se<sub>2</sub> (bulk)/NiSe (surface) into nickel oxyhydroxide. …”
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14165
Morphological Degradation of Oxygen Evolution Reaction-Electrocatalyzing Nickel Selenides at Industrially Relevant Current Densities
Published 2025“…Morphological degradation of the catalyst material was only observed at current densities exceeding 1 A cm<sup>–2</sup> but not for smaller ones. Using X-ray absorption, X-ray photoemission spectroscopy, and X-ray diffraction, we confirmed that the degradation was accompanied by the literature-known transformation of nanoparticulate Ni<sub>3</sub>Se<sub>2</sub> (bulk)/NiSe (surface) into nickel oxyhydroxide. …”
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14166
Morphological Degradation of Oxygen Evolution Reaction-Electrocatalyzing Nickel Selenides at Industrially Relevant Current Densities
Published 2025“…Morphological degradation of the catalyst material was only observed at current densities exceeding 1 A cm<sup>–2</sup> but not for smaller ones. Using X-ray absorption, X-ray photoemission spectroscopy, and X-ray diffraction, we confirmed that the degradation was accompanied by the literature-known transformation of nanoparticulate Ni<sub>3</sub>Se<sub>2</sub> (bulk)/NiSe (surface) into nickel oxyhydroxide. …”
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14167
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14168
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14169
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14170
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14171
Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
Published 2020“…The charge delocalization between the <i>N</i>-heterocyclic carbene (NHC) and the metal in cationic molybdenum imido alkylidene NHC mono(nonafluoro-<i>tert</i>-butoxide) complexes has been studied for different NHCs, i.e., 1,3-dimesitylimidazol-2-ylidene (IMes), 1,3-dimesityl-4,5-dichloroimidazol-2-ylidene (IMesCl<sub>2</sub>), 1,3-dimesityl-4,5-dimethylimidazol-2-ylidene (IMesMe<sub>2</sub>), and 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene (IMesH<sub>2</sub>). …”
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14172
Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
Published 2020“…The charge delocalization between the <i>N</i>-heterocyclic carbene (NHC) and the metal in cationic molybdenum imido alkylidene NHC mono(nonafluoro-<i>tert</i>-butoxide) complexes has been studied for different NHCs, i.e., 1,3-dimesitylimidazol-2-ylidene (IMes), 1,3-dimesityl-4,5-dichloroimidazol-2-ylidene (IMesCl<sub>2</sub>), 1,3-dimesityl-4,5-dimethylimidazol-2-ylidene (IMesMe<sub>2</sub>), and 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene (IMesH<sub>2</sub>). …”
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14173
Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
Published 2020“…The charge delocalization between the <i>N</i>-heterocyclic carbene (NHC) and the metal in cationic molybdenum imido alkylidene NHC mono(nonafluoro-<i>tert</i>-butoxide) complexes has been studied for different NHCs, i.e., 1,3-dimesitylimidazol-2-ylidene (IMes), 1,3-dimesityl-4,5-dichloroimidazol-2-ylidene (IMesCl<sub>2</sub>), 1,3-dimesityl-4,5-dimethylimidazol-2-ylidene (IMesMe<sub>2</sub>), and 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene (IMesH<sub>2</sub>). …”
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14174
Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
Published 2020“…The charge delocalization between the <i>N</i>-heterocyclic carbene (NHC) and the metal in cationic molybdenum imido alkylidene NHC mono(nonafluoro-<i>tert</i>-butoxide) complexes has been studied for different NHCs, i.e., 1,3-dimesitylimidazol-2-ylidene (IMes), 1,3-dimesityl-4,5-dichloroimidazol-2-ylidene (IMesCl<sub>2</sub>), 1,3-dimesityl-4,5-dimethylimidazol-2-ylidene (IMesMe<sub>2</sub>), and 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene (IMesH<sub>2</sub>). …”
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14175
Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
Published 2020“…The charge delocalization between the <i>N</i>-heterocyclic carbene (NHC) and the metal in cationic molybdenum imido alkylidene NHC mono(nonafluoro-<i>tert</i>-butoxide) complexes has been studied for different NHCs, i.e., 1,3-dimesitylimidazol-2-ylidene (IMes), 1,3-dimesityl-4,5-dichloroimidazol-2-ylidene (IMesCl<sub>2</sub>), 1,3-dimesityl-4,5-dimethylimidazol-2-ylidene (IMesMe<sub>2</sub>), and 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene (IMesH<sub>2</sub>). …”
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14176
Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach
Published 2020“…The charge delocalization between the <i>N</i>-heterocyclic carbene (NHC) and the metal in cationic molybdenum imido alkylidene NHC mono(nonafluoro-<i>tert</i>-butoxide) complexes has been studied for different NHCs, i.e., 1,3-dimesitylimidazol-2-ylidene (IMes), 1,3-dimesityl-4,5-dichloroimidazol-2-ylidene (IMesCl<sub>2</sub>), 1,3-dimesityl-4,5-dimethylimidazol-2-ylidene (IMesMe<sub>2</sub>), and 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene (IMesH<sub>2</sub>). …”
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14177
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14178
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14179
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14180