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Aerobic Oxidation of Alcohols on Au Nanocatalyst: Insight to the Roles of the Ni–Al Layered Double Hydroxides Support
Author(s) -
Wang Jiang,
Lang Xianjun,
Zhaorigetu Bao,
Jia Meilin,
Wang Jun,
Guo Xiaofang,
Zhao Jincai
Publication year - 2014
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201400046
Subject(s) - layered double hydroxides , catalysis , redox , hydroxide , alcohol oxidation , nanoparticle , inorganic chemistry , chemistry , base (topology) , hydrotalcite , chemical engineering , materials science , nanotechnology , organic chemistry , mathematical analysis , mathematics , engineering
Au nanoparticles (NPs) supported on Ni–Al layered double hydroxides (LDHs) were shown to be efficient heterogeneous catalysts for the highly selective oxidation of alcohols to the corresponding aldehydes or ketones under base‐free or even solvent‐free conditions with O 2 as the sole oxidant. The Au NPs can be uniformly distributed on Ni–Al LDHs support, which is beneficial to the catalytic activity. In addition, the weak Brønsted basic property of the support enables the aerobic oxidation of alcohols under base‐free conditions. More importantly, unlike Al 2 O 3 , which is inert, Ni–Al–LDHs are redox‐actively involved in prompting the electron transfer to O 2 via the Au nanocatalyst because of the presence of Ni II . Both of the basic and the redox properties of Ni–Al–LDHs can be tuned by adjusting the ratio of Ni:Al to achieve the best synergistic effects between Au NPs and the supports. The activity of the obtained Au catalysts was found to be structurally associated with the arrangements of NiO 6 and AlO 6 octahedra in the surface hydroxide layers which were different from the bulk Ni:Al ratio.