Showing 14,161 - 14,180 results of 122,625 for search '(( 2 e decrease ) OR ( 5 ((((ng decrease) OR (a decrease))) OR (mean decrease)) ))', query time: 2.15s Refine Results
  1. 14161
  2. 14162

    Configuring Bonds between First-Row Transition Metals by Reed J. Eisenhart (1469023)

    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>. …”
  3. 14163

    Configuring Bonds between First-Row Transition Metals by Reed J. Eisenhart (1469023)

    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>. …”
  4. 14164

    Morphological Degradation of Oxygen Evolution Reaction-Electrocatalyzing Nickel Selenides at Industrially Relevant Current Densities by Felix Hiege (21700895)

    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. …”
  5. 14165

    Morphological Degradation of Oxygen Evolution Reaction-Electrocatalyzing Nickel Selenides at Industrially Relevant Current Densities by Felix Hiege (21700895)

    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. …”
  6. 14166

    Morphological Degradation of Oxygen Evolution Reaction-Electrocatalyzing Nickel Selenides at Industrially Relevant Current Densities by Felix Hiege (21700895)

    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. …”
  7. 14167
  8. 14168
  9. 14169
  10. 14170
  11. 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 by Mathis Benedikter (9726148)

    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>). …”
  12. 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 by Mathis Benedikter (9726148)

    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>). …”
  13. 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 by Mathis Benedikter (9726148)

    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>). …”
  14. 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 by Mathis Benedikter (9726148)

    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>). …”
  15. 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 by Mathis Benedikter (9726148)

    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>). …”
  16. 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 by Mathis Benedikter (9726148)

    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>). …”
  17. 14177
  18. 14178
  19. 14179
  20. 14180