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One‐Pot Fabrication of Pd Nanoparticles@Covalent‐Organic‐Framework‐Derived Hollow Polyamine Spheres as a Synergistic Catalyst for Tandem Catalysis
Author(s) -
Yang Xinyi,
He Yajun,
Li Liuyi,
Shen Jinni,
Huang Jianhui,
Li Lingyun,
Zhuang Zanyong,
Bi Jinhong,
Yu Yan
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201904731
Subject(s) - ammonia borane , catalysis , nanomaterial based catalyst , nanoparticle , dehydrogenation , chemistry , imine , bimetallic strip , combinatorial chemistry , covalent bond , chemical engineering , nanotechnology , tandem , molecule , materials science , organic chemistry , engineering , composite material
Facile fabrication of nanocatalysts consisting of metal nanoparticles (NPs) anchored on a functional support is highly desirable, yet remains challenging. Covalent organic frameworks (COFs) provide an emerging materials platform for structural control and functional design. Here, a facile one‐pot in situ reduction approach is demonstrated for the encapsulation of small Pd NPs into the shell of COF‐derived hollow polyamine spheres (Pd@H‐PPA). In the one‐pot synthetic process, the nucleation and growth of Pd NPs in the cavities of the porous shell take place simultaneously with the reduction of imine linkages to secondary amine groups. Pd@H‐PPA shows a significantly enhanced catalytic activity and recyclability in the tandem dehydrogenation of ammonia borane and selective hydrogenation of nitroarenes through an adsorption–activation–reaction mechanism. The strong interactions of the secondary amine linkage with borane and nitroarene molecules afford a positive synergy to promote the catalytic reaction. Moreover, the hierarchical structure of Pd@H‐PPA allows the accessibility of active Pd NPs to reactants.