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 using a bulky diphosphine, dppeF (1,2-bis[bis(3,5-ditrifluoromethylphenyl)phosphino]ethane) as a protecting ligand. Single-crystal X-ray diffraction analysis revealed that this nanocluster has an icosahedral Au13 core, which is protected by each of three Cl ligands on opposite poles and by three dppeF ligands in an equatorial plane. This nanocluster acted as a homogeneous catalyst for hydroamination between phenylacetylene and aniline, facilitated by the rapid exchange of the Cl− ligands with phenyl acetylides.
- This article is part of the themed collection: Advances in computational chemistry and catalysis: Honouring Jumras Limtrakul’s 72nd birthday

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