4.8 Article

Heterogeneously Catalyzed Selective Decarbonylation of Aldehydes by CeO2-Supported Highly Dispersed Non-Electron-Rich Ni(0) Nanospecies

Journal

ACS CATALYSIS
Volume 11, Issue 22, Pages 13745-13751

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c03375

Keywords

nickel; ceria; aldehydes; decarbonylation; heterogeneous catalysts

Funding

  1. JSPS KAKENHI [19H02509, 21K14460]
  2. Nanotechnology Platform of the Ministry of Education, Culture, Sports, Science and Technology (MEXT) ,Japan
  3. Grants-in-Aid for Scientific Research [21K14460, 19H02509] Funding Source: KAKEN

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A highly efficient selective aldehyde decarbonylation reaction has been developed using a heterogeneous Ni(0) nanospecies catalyst supported on CeO2, with a broad substrate scope and functional group tolerance. The high catalytic performance is attributed to the highly dispersed and non-electron-rich N(0) nanospecies, which suppress side reactions and CO-derived inhibition of catalytic turnover.
Aldehyde decarbonylation has been extensively investigated, primarily using noble-metal catalysts; however, nonprecious-base-metal-catalyzed aldehyde decarbonylation has been hardly reported. We have established an efficient selective aldehyde decarbonylation reaction with a broad substrate scope and functional group tolerance utilizing a heterogeneous Ni(0) nanospecies catalyst supported on CeO2. The high catalytic performance is attributable to the highly dispersed and non-electron-rich N(0) nanospecies, which possibly suppress a side reaction producing esters and adsorbed CO-derived inhibition of the catalytic turnover, according to detailed catalyst characterization and kinetic evaluation.

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