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    Hydrosilylation is one of the largest-scale applications for homogeneous catalysis and is widely used to enable the commercial manufacture of silicon products. In this paper, a bifunctional heterogeneous catalyst, Pt δ+/AET-MIL-101 (AET = 2-aminoethanethiol) with a partially positively charged Pt δ+ electronic structure is reported, which was successfully prepared using post-synthesis modification with AET and a platinum precursor. The catalysts were characterized using X-ray diffraction (XRD), nitrogen (N2) adsorption-desorption, transmission electron microscopy (TEM), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) techniques which showed that the synergy of AET-MIL-101 provides a good dispersion of Pt δ+ in the channels, which can efficiently catalyze the hydrosilylation reaction with almost complete conversion and produce a unique adduct. In addition, the synthetic heterogeneous catalyst Pt δ+/AET-MIL-101 achieves reasonable use of Pt in terms of number cycles and atomic utilization efficiency, indicating the potential to achieve a green hydrosilylation industry. This journal is © The Royal Society of Chemistry.

    Citation

    Zhikai Xie, Weiwen Chen, Xiuying Chen, Xinhua Zhou, Wenbin Hu, Xugang Shu. Platinum on 2-aminoethanethiol functionalized MIL-101 as a catalyst for alkene hydrosilylation. RSC advances. 2019 Jun 25;9(35):20314-20322


    PMID: 35514732

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