Journal article Chemical synthesis of Zr-/Ce-/Sm-containing intermetallic compounds catalyzing NaBH 4 -assisted hydrogenation of 4-nitrophenol
Yasukazu Kobayashi (author) (Search by this author)
;
Hiroshi Mizoguchi (author) (Search by this author)
ORCID SAMURAI ;
Koharu Yamamoto (author) (Search by this author)
;
Ryo Shoji (author) (Search by this author)
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Citation
Yasukazu Kobayashi, Hiroshi Mizoguchi, Koharu Yamamoto, Ryo Shoji. Chemical synthesis of Zr-/Ce-/Sm-containing intermetallic compounds catalyzing NaBH 4 -assisted hydrogenation of 4-nitrophenol. Dalton Transactions. 2026, 55 (17), 6876-6885. https://doi.org/10.1039/d6dt00513f

Description:

(abstract)

Zr-/Ce-/Sm-containing intermetallic compounds, specifically ZrZnNi4, CeNi5, CeAlNi4, CeNi4Si, Ce(NiSi)2, SmNi3, SmNi4Si, and Sm(NiSi)2, were synthesized by reducing the metal oxides using a CaH2 reducing agent within molten LiCl. The resultant nanopowders exhibited high specific surface areas: ZrZnNi4 (42.0 m2/g), CeAlNi4 (66.9 m2/g), and Sm(NiSi)2 (25.0 m2/g). They were subsequently tested for their effectiveness in the NaBH4-assisted hydrogenation of 4-nitrophenol. When compared to the prepared catalysts, including a conventional CeO2-supported Ni catalyst, ZrZnNi4 demonstrated the highest catalytic activity. Based on experimental results and density functional theory calculations, it was proposed that this enhanced performance could be attributed to the formation of electron-rich Ni species in ZrZnNi4.

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Keyword: catalysts

Date published: 2026-04-17

Publisher: Royal Society of Chemistry (RSC)

Journal:

  • Dalton Transactions (ISSN: 14779234) vol. 55 issue. 17 p. 6876-6885

Funding:

  • Ministry of Education, Culture, Sports, Science and Technology JPMXP125NM5175
  • Japan Society for the Promotion of Science 23K23440
  • Japan Society for the Promotion of Science 24K08591

Manuscript type: Publisher's version (Version of record)

MDR DOI:

First published URL: https://doi.org/10.1039/d6dt00513f

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Updated at: 2026-05-11 11:00:05 +0900

Published on MDR: 2026-05-11 12:24:43 +0900

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