TY - JOUR
T1 - Unsupported Nanoporous Gold Catalyst for Chemoselective Hydrogenation Reactions under Low Pressure
T2 - Effect of Residual Silver on the Reaction
AU - Takale, Balaram S.
AU - Feng, Xiujuan
AU - Lu, Ye
AU - Bao, Ming
AU - Jin, Tienan
AU - Minato, Taketoshi
AU - Yamamoto, Yoshinori
N1 - Funding Information:
We acknowledge Prof. T. Fujita at WPI-AIMR for useful discussions on structural details of nanoporous gold. We are grateful to the National Natural Science Foundation of China (Nos. 21373041, 21372035) and NSFC-IUPAC program (No. 21361140375) for their financial support. This work was supported by KAKENHI (Grant-in-Aid for Scientific Research (A), 23245020). T.J. acknowledges JSPS KAKENHI Grant No. JP16H01000 in Precisely Designed Catalysts with Customized Scaffolding
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/8/17
Y1 - 2016/8/17
N2 - For the first time, H-H dissociation on an unsupported nanoporous gold (AuNPore) surface is reported for chemoselective hydrogenation of C=C, C=C, C=N, and C=O bonds under mild conditions (8 atm H2 pressure, 90 °C). Silver doping in AuNPore, which was inevitable for its preparation through a process of dealloying of Au-Ag alloy, exhibited a remarkable difference in catalytic activity between two catalysts, Au>99Ag1NPore and Au90Ag10NPore.The former was more active and the latter less active in H2 hydrogenation, while the reverse tendency was observed for O2 oxidation. This marked contrast between H2 reduction and O2 oxidation is discussed. Further, Au>99Ag1NPore showed a high chemoselectivity toward reduction of terminal alkynes in the presence of internal alkynes which was not achieved using supported gold nanoparticle catalysts and other previously known methods. Reductive amination, which has great significance in synthesis of amines due to its atom-economical nature, was also realized using Au>99Ag1NPore, and the Au>99Ag1NPore/H2 system showed a preference for the reduction of aldehydes in the presence of imines. In addition to this high chemoselectivity, easy recovery and high reusability of AuNPore make it a promising heterogeneous catalyst for hydrogenation reactions.
AB - For the first time, H-H dissociation on an unsupported nanoporous gold (AuNPore) surface is reported for chemoselective hydrogenation of C=C, C=C, C=N, and C=O bonds under mild conditions (8 atm H2 pressure, 90 °C). Silver doping in AuNPore, which was inevitable for its preparation through a process of dealloying of Au-Ag alloy, exhibited a remarkable difference in catalytic activity between two catalysts, Au>99Ag1NPore and Au90Ag10NPore.The former was more active and the latter less active in H2 hydrogenation, while the reverse tendency was observed for O2 oxidation. This marked contrast between H2 reduction and O2 oxidation is discussed. Further, Au>99Ag1NPore showed a high chemoselectivity toward reduction of terminal alkynes in the presence of internal alkynes which was not achieved using supported gold nanoparticle catalysts and other previously known methods. Reductive amination, which has great significance in synthesis of amines due to its atom-economical nature, was also realized using Au>99Ag1NPore, and the Au>99Ag1NPore/H2 system showed a preference for the reduction of aldehydes in the presence of imines. In addition to this high chemoselectivity, easy recovery and high reusability of AuNPore make it a promising heterogeneous catalyst for hydrogenation reactions.
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U2 - 10.1021/jacs.6b06569
DO - 10.1021/jacs.6b06569
M3 - Article
AN - SCOPUS:84983404578
SN - 0002-7863
VL - 138
SP - 10356
EP - 10364
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 32
ER -