N-heterocyclic carbene-stabilized metal nanoparticles within porous organic cages for catalytic application

被引:27
|
作者
Liu, Tong [1 ]
Bai, Sha [1 ]
Zhang, Le [1 ]
Hahn, F. Ekkehardt [1 ,2 ]
Han, Ying-Feng [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Xian Key Lab Funct Supramol Struct & Mat, Key Lab Synthet & Nat Funct Mol,Minist Educ, Xian 710127, Peoples R China
[2] Westfalische Wilhelms Univ Munster, Inst Anorganicshe & Analyt Chem, D-48149 Munster, Germany
关键词
metal nanoparticle; porous organic cage; catalytic reaction; N-heterocyclic carbene; PALLADIUM NANOPARTICLES; HETEROGENEOUS CATALYSTS; GOLD NANOPARTICLES; TEMPLATE SYNTHESIS; COORDINATION; COMPLEXES; EFFICIENT; LIGANDS;
D O I
10.1093/nsr/nwac067
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tuning the surface-embellishing ligands of metal nanoparticles (NPs) is a powerful strategy to modulate their morphology and surface electronic and functional features, impacting their catalytic activity and selectivity. In this work, we report the design and synthesis of a polytriazolium organic cage PIC-T, capable of stabilizing PdNPs within its discrete cavity. The obtained material (denoted Pd@PCC-T) is highly durable and monodispersed with narrow particle-size distribution of 2.06 +/- 0.02 nm, exhibiting excellent catalytic performance and recyclability in the Sonogashira coupling and tandem reaction to synthesize benzofuran derivatives. Further investigation indicates that the modulation of N-heterocyclic carbene sites embedded in the organic cage has an impact on NPs' catalytic efficiency, thus providing a novel methodology to design superior NP catalysts. The discrete cage structure and a subtle regulation of NHC sites inside the cavity facilitate the controllable formation of unique PdNPs with superior catalytic performances.
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页数:8
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