Copper nanoparticle heterogeneous catalytic 'click' cycloaddition confirmed by single-molecule spectroscopy

被引:131
作者
Decan, Matthew R. [1 ,2 ]
Impellizzeri, Stefania [1 ,2 ]
Luisa Marin, M. [1 ,2 ,3 ]
Scaiano, Juan C. [1 ,2 ]
机构
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Ctr Catalysis Res & Innovat, Ottawa, ON K1N 6N5, Canada
[3] Univ Politecn Valencia, CSIC, Inst Univ Mixto Tecnol Quim, Valencia 46022, Spain
基金
加拿大自然科学与工程研究理事会;
关键词
ALKYNE-AZIDE CYCLOADDITION; MULTICOMPONENT SYNTHESIS; MECHANISTIC INSIGHTS; GOLD NANOPARTICLES; TERMINAL ALKYNES; HIGH-RESOLUTION; CHEMISTRY; REACTIVITY; DYNAMICS; 1,2,3-TRIAZOLES;
D O I
10.1038/ncomms5612
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
Colloidal or heterogeneous nanocatalysts can improve the range and diversity of Cu(I)catalysed click reactions and facilitate catalyst separation and reuse. Catalysis by metal nanoparticles raises the question as to whether heterogeneous catalysts may cause homogeneous catalysis through metal ion leaching, since the catalytic process could be mediated by the particle, or by metal ions released from it. The question is critical as unwanted homogeneous processes could offset the benefits of heterogeneous catalysis. Here, we combine standard bench scale techniques with single-molecule spectroscopy to monitor single catalytic events in real time and demonstrate that click catalysis occurs directly at the surface of copper nanoparticles; this general approach could be implemented in other systems. We use 'from the mole to the molecule' to describe this emerging idea in which mole scale reactions can be optimized through an intimate understanding of the catalytic process at the single-molecule-single catalytic nanoparticle level.
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页数:8
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