Pd/N, S co-doped activated carbon as a highly-efficient catalyst for the one-pot synthesis of meropenem

被引:1
|
作者
Li, Yuefeng [1 ,2 ,3 ]
Xiong, Fengmei [4 ]
Yan, Jiangmei [2 ,3 ]
Wang, Zhaowen [2 ,3 ]
Hong, Tao [1 ]
Zhang, Zhixiang [2 ,3 ]
Li, Yu [1 ]
Jing, Xinli [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem, Xian 710049, Shaanxi, Peoples R China
[2] Kaili Catalyst & New Mat Co Ltd, Dept Technol, Xian 710201, Shaanxi, Peoples R China
[3] Shaanxi Key Lab Catalyt Mat & Technol, Xian 710201, Shaanxi, Peoples R China
[4] Xian Childrens Hosp, Dept Pharm, Xian 710004, Shaanxi, Peoples R China
基金
国家重点研发计划;
关键词
SELECTIVE HYDROGENATION; SULFUR RESISTANCE; CODOPED GRAPHENE; HIGH-PERFORMANCE; REDUCTION; NITROGEN; ACID; DEBENZYLATION; SUPPORT; PRECURSOR;
D O I
10.1039/d2cy02100e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
N, S co-doped active carbons (ACs) were synthesized and utilized as supports to prepare palladium/activated carbon (Pd/C) catalysts. Characterization of the as-prepared supports suggested that the variety of surface functional groups impacted Pd nanoparticles (NPs) with regard to particle size, chemical state, and dispersion. N, S co-doped activated carbon-supported Pd nanoparticles modified with 3 wt% sulfur with a reduced size distribution of approximately 1.81 nm exhibited substantially enhanced activity for the one-pot synthesis of meropenem and provided a higher meropenem yield compared to other Pd/C catalysts. The nitrogen and sulfur groups provided efficient anchoring sites to facilitate Pd NPs dispersion onto the AC surface, which facilitated electron transformation between the supports and the Pd nanoparticles, and contributed to forming relatively electron-deficient, ultra-low size Pd NPs, thereby improving the anti-poisoning performance of Pd/C catalysts, leading to high hydrogenation activity.
引用
收藏
页码:1686 / 1695
页数:10
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