| Literature DB >> 35261133 |
Hao Yan1, Mingyue Zhao1, Xiang Feng1, Siming Zhao1, Xin Zhou1, Shangfeng Li1, Minghao Zha1, Fanyu Meng1, Xiaobo Chen1, Yibin Liu1, Ning Yan2, Chaohe Yang1.
Abstract
Achieving efficient catalytic conversion over a heterogeneous catalyst with excellent resistance against leaching is still a grand challenge for sustainable chemical synthesis in aqueous solution. Herein, we devised a single-atom Pt1 /hydroxyapatite (HAP) catalyst via a simple hydrothermal strategy. Gratifyingly, this robust Pt1 /HAP catalyst exhibits remarkable catalytic selectivity and catalyst stability for the selective oxidation of C2 -C4 polyols to corresponding primary hydroxy acids. It is found that the Pt-(O-P) linkages with strong electron-withdrawing function of PO4 3- (Pt1 -OPO4 3- pair active site) not only realize the activation of the C-H bond, but also destabilize the transition state from adsorbed hydroxy acids toward the C-C cleavage, resulting in the sharply increased selectivity of hydroxy acids. Moreover, the strong PO4 3- -coordination effect provides electrostatic stabilization for single-atom Pt, ensuring the highly efficient catalysis of Pt1 /HAP for over 160 hours with superior leaching resistance.Entities:
Keywords: Coordination Effects; Hydroxyl Acid; Polyols; Selective Oxidation; Single-Atom Catalysts
Year: 2022 PMID: 35261133 DOI: 10.1002/anie.202116059
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336