环己酮
化学
催化作用
醛
亲核细胞
金属羰基
纳米颗粒
吸附
金属
大气压力
光化学
无机化学
有机化学
核化学
材料科学
纳米技术
地质学
海洋学
作者
Shotaro Matsuda,Shinya Masuda,Shinjiro Takano,Nobuyuki Ichikuni,Tatsuya Tsukuda
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2021-08-09
卷期号:11 (16): 10502-10507
被引量:6
标识
DOI:10.1021/acscatal.1c02703
摘要
Poly(vinylpyrrolidone) (PVP)-stabilized Ir- or Pt-doped (10 at. %) Ru NPs with the average diameters of 1.3–1.5 nm (RuIr or RuPt) were prepared by a coreduction of the corresponding metal precursors. RuIr and RuPt showed remarkable activity for the hydrogenation of aromatic, cyclic, and aliphatic carbonyl compounds at 30 °C under 0.2 MPa of H2, whereas the monometallic NPs of Ru, Ir, and Pt did not show any activity under the same conditions. In particular, RuPt converted the aliphatic aldehyde and cyclohexanone to the corresponding alcohols at 30 °C under atmospheric H2 pressure. Remarkable synergistic effects were ascribed to the provision of highly active sites for H2 and enhancement of the nucleophilicity of the adsorbed hydrides.
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