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Kinetically controlled synthesis of Au-102(SPh)(44) nanoclusters and catalytic application

机译:活动的可控合成非盟- 102 (SPh)(44)制备和催化应用程序

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摘要

We here explore a kinetically controlled synthetic protocol for preparing solvent-solvable Au-102(SPh)(44) nanoclusters which are isolated from polydispersed gold nanoclusters by solvent extraction and size exclusion chromatography (SEC). The as-obtained Au-102(SPh)(44) nanoclusters are determined by matrix-assisted laser desorption ionization (MALDI) and electrospray ionization (ESI) mass spectrometry, in conjunction with UV-vis spectroscopy and thermogravimetric analysis (TGA). However, Au-99(SPh)(42), instead of Au-102(SPh)(44), is yielded when the polydispersed gold nanoclusters are etched in the presence of excess thiophenol under thermal conditions (e.g., 80 degrees C). Interestingly, the Au-102(SPh)(44) nanoclusters also can convert to Au-99(SPh)(42) with equivalent thiophenol ligands, evidenced by the analyses of UV-vis and MALDI mass spectrometry. Finally, the TiO2-supported Au-102(SPh)(44) nanocluster catalyst is investigated in the selective oxidation of sulfides into sulfoxides by the PhIO oxidant and gives rise to high catalytic activity (e.g., 80-99% conversion of R-S-R' sulfides with 96-99% selectivity for R-S(vO)-R' sulfoxides). The Au-102(SPh)(44)/TiO2 catalyst also shows excellent recyclability in the sulfoxidation process.
机译:我们在这里探讨合成控制的活动协议准备solvent-solvable非盟- 102 (SPh)(44)制备分离多分散的金纳米束的溶剂提取和尺寸排阻色谱法(SEC)。束是由matrix-assisted决定的激光解吸电离(MALDI)和电喷雾电离质谱(ESI),结合紫外可见光谱和热重分析(TGA)。au - 99 (SPh)(42),而非盟- 102 (SPh) (44)多分散的金纳米束时产生铭刻在过量的苯硫酚的存在吗热条件下(例如,80摄氏度)。有趣的是,非盟- 102 (SPh)(44)发光机制也可以转换为非盟- 99 (SPh) (42)与苯硫酚配体,证明了这一点分析紫外可见和谱质谱。最后,TiO2-supported au - 102 (SPh) (44)研究在纳米催化剂硫化物的选择性氧化为亚砜PhIO氧化剂和产生高催化活性(如,80 - 99%的转换R-S-R的硫化物选择性为96 - 99%R-S(旁白)-R’sulfoxides)。催化剂还显示了出色的再循环能力sulfoxidation过程。

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