Affiliation:
1. International Research Center for Elements Science Institute for Chemical Research Kyoto University Uji Kyoto 611-0011 Japan
2. Department of Energy and Hydrocarbon Chemistry Graduate School of Engineering Kyoto University Nishikyo-ku Kyoto 615-8510 Japan
Abstract
AbstractThiolate‐protected gold nanoclusters (AuNCs) have attracted significant attention as nano‐catalysts, revealing a superatomic core and gold‐thiolate staples as distinct structural units. Here, we demonstrate the unprecedented dual catalytic activity of thiolate‐protected [Au25(SR)18]− nanoclusters, involving both photosensitized 1O2 generation by the Au13 superatomic core and catalytic carbon‐carbon bond formation facilitated by Au2(SR)3 staples. This synergistic combination of two different catalytic units enables efficient cross‐dehydrogenative coupling of terminal alkynes and tertiary aliphatic amines to afford propargylamines in high yields of up to 93 %. Mixed‐ligand AuNCs bearing both thiolate and alkynyl ligands revealed the intermediacy of the alkynyl‐exchanged AuNCs toward both photosensitization and C−C bond‐forming catalytic cycles. Density functional theory calculations also supported the intermediacy of the alkynyl‐exchanged AuNCs. Thus, the use of ligand‐protected metal nanoclusters has enabled the development of an exceptional multifunctional catalyst, wherein distinct nanocluster components facilitate cooperative photo‐ and chemo‐catalysis.
Funder
Japan Society for the Promotion of Science
Kyoto University Foundation
Iketani Science and Technology Foundation
Hitachi Metals · Materials Science Foundation
Subject
General Chemistry,Catalysis
Cited by
4 articles.
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