An icosahedral Au13 nanocluster with three adjacent chlorides on opposite poles catalyses hydroamination of phenylacetylene
Abstract
A novel anionic gold nanocluster [Au13(dppeF)3Cl6]– bearing six chlorides has been synthesized by using a bulky diphosphine, dppeF (1,2-bis[bis(3,5-ditrifluoromethylphenyl)phosphino]ethane), as protecting ligands. Single-crystal X-ray diffraction analysis of this nanocluster revealed that an icosahedral Au13 core is protected by a total of six chlorides, evenly distributed at opposite poles, and by three dppeF ligands on an equatorial plane. This nanocluster acted as a homogeneous catalyst for hydroamination between phenylacetylene and aniline facilitated by the rapid exchange of the chlorides with phenylacetylides.
- This article is part of the themed collection: Advances in computational chemistry and catalysis: Honouring Jumras Limtrakul’s 72nd birthday
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