Tsunoyama Hironori, Ichikuni Nobuyuki, Sakurai Hidehiro, Tsukuda Tatsuya
Catalysis Research Center, Hokkaido University, Nishi 10, Kita 21, Sapporo 001-0021, Japan.
J Am Chem Soc. 2009 May 27;131(20):7086-93. doi: 10.1021/ja810045y.
Au clusters smaller than 1.5 nm and stabilized by poly(N-vinyl-2-pyrrolidone) (PVP) showed higher activity for aerobic oxidation of alcohol than those of larger size or stabilized by poly(allylamine) (PAA). X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy of adsorbed CO, and X-ray absorption near edge structure measurements revealed that the catalytically active Au clusters are negatively charged by electron donation from PVP, and the catalytic activity is enhanced with increasing electron density on the Au core. Based on similar observations of Au cluster anions in the gas phase, we propose that electron transfer from the anionic Au cores of Au:PVP into the LUMO (pi*) of O(2) generates superoxo- or peroxo-like species, which plays a key role in the oxidation of alcohol. On the basis of these results, a simple principle is presented for the synthesis of Au oxidation catalysts stabilized by organic molecules.
由聚(N-乙烯基-2-吡咯烷酮)(PVP)稳定的小于1.5纳米的金簇对醇的有氧氧化显示出比更大尺寸或由聚烯丙胺(PAA)稳定的金簇更高的活性。X射线光电子能谱、吸附CO的傅里叶变换红外光谱以及X射线吸收近边结构测量表明,催化活性金簇通过PVP的电子给予而带负电荷,并且催化活性随着金核上电子密度的增加而增强。基于对气相中金簇阴离子的类似观察,我们提出从Au:PVP的阴离子金核到O(2)的LUMO(π*)的电子转移产生超氧或过氧样物种,其在醇的氧化中起关键作用。基于这些结果,提出了一种合成由有机分子稳定的金氧化催化剂的简单原理。