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Platinum on 2-aminoethanethiol functionalized MIL-101 as a catalyst for alkene hydrosilylation.


ABSTRACT: 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.

SUBMITTER: Xie Z 

PROVIDER: S-EPMC9065458 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Platinum on 2-aminoethanethiol functionalized MIL-101 as a catalyst for alkene hydrosilylation.

Xie Zhikai Z   Chen Weiwen W   Chen Xiuying X   Zhou Xinhua X   Hu Wenbin W   Shu Xugang X  

RSC advances 20190628 35


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 <sup><i>δ</i>+</sup>/AET-MIL-101 (AET = 2-aminoethanethiol) with a partially positively charged Pt <sup><i>δ</i>+</sup> electronic structure is reported, which was successfully prepared using post-synthesis modification with AET and a platinum precursor. The catalysts were character  ...[more]

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