化学
苯乙炔
催化作用
共价有机骨架
选择性
苯乙烯
钯
共价键
贵金属
色散(光学)
化学工程
乙炔
复合数
共聚物
有机化学
复合材料
聚合物
材料科学
工程类
物理
光学
作者
Jianhong Li,Zhi Yu,Zhi Gao,Jian Qiang Li,Yuan Tao,Yu Xiao,Wen Yin,Ya Ling Fan,Chao Jiang,Li Sun,Feng Luo
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2019-08-01
卷期号:58 (16): 10829-10836
被引量:31
标识
DOI:10.1021/acs.inorgchem.9b01117
摘要
Developing noble-metal-based catalysts with ultralow loading to achieve excellent performance for selective hydrogenation of alkynes under mild reaction conditions is highly desirable but still faces huge challenges. To this end, a SO3H-anchored covalent organic framework (COF-SO3H) as the support was deliberately designed, and then ultralow-content Pd (0.38 wt %) was loaded by a wet-chemistry immersion dispersion method. The resulting Pd0.38/COF-SO3H composite exhibits outstanding performance for the selective hydrogenation of phenylacetylene with 97.06% conversion and 93.15% selectivity to styrene under mild reaction conditions (1 bar of H2, 25 °C). Noticeably, the turnover frequency value reaches as high as 3888 h–1, which outperforms most of reported catalysts for such use. Moreover, such a catalyst also exhibits excellent activity for a series of other alkynes and high stability without obvious loss of catalytic performance after five consecutive cycles.
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