| Literature DB >> 31971660 |
Rao Tao1, Xiran Shen1, Yiming Hu2, Kun Kang1, Yaqian Zheng1, Shichang Luo1, Shiyu Yang3, Wenliang Li4, Shuanglong Lu5, Yinghua Jin2, Li Qiu1, Wei Zhang2.
Abstract
In this work, a phosphine-based covalent organic framework (Phos-COF-1) is successfully synthesized and employed as a template for the confined growth of broad-scope nanoparticles (NPs). Ascribed to the ordered distribution of phosphine coordination sites in the well-defined pores, various stable and well-dispersed ultrafine metal NPs including Pd, Pt, Au, and bimetallic PdAuNPs with narrow size distributions are successfully prepared as determined by transmission electron microscopy, X-ray photoelectron spectroscopy, inductively coupled plasma, and powder X-ray diffraction analyses. It is also demonstrated that the as-prepared Phos-COF-1-supported ultrafine NPs exhibit excellent catalytic activities and recyclability toward the Suzuki-Miyaura coupling reaction, reduction of nitro-phenol and 1-bromo-4-nitrobenzene, and even tandem coupling and reduction of p-nitroiodobenzene. This work will open many new possibilities for preparing COF-supported ultrafine NPs with good dispersity and stability for a broad range of applications.Entities:
Keywords: catalysis; controlled synthesis; covalent organic frameworks; metal nanoparticles; phosphine
Year: 2020 PMID: 31971660 DOI: 10.1002/smll.201906005
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281