Abstract
AbstractThe first C3‐symmetric 44‐core‐valence‐electron triangular palladium clusters, [{(SAr′)(PAr3)Pd}3]+, have been synthesized by activation of the CS bond of isothioureas. Owing to delocalized metal–metal bonding, these stable complexes are the first noble‐metal analogues of the π‐aromatic cyclopropenyl cation [C3H3]+, with their all‐metal aromaticity involving d‐type atomic orbitals.
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