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Synthesis of Triangular Tripalladium Cations as Noble‐Metal Analogues of the Cyclopropenyl Cation
Author(s) -
Blanchard Sébastien,
Fensterbank Louis,
Gontard Geoffrey,
Lacôte Emmanuel,
Maestri Giovanni,
Malacria Max
Publication year - 2014
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201310204
Subject(s) - delocalized electron , chemistry , aromaticity , metal , noble metal , electron delocalization , palladium , valence (chemistry) , atomic orbital , crystallography , inorganic chemistry , photochemistry , electron , molecule , catalysis , organic chemistry , physics , quantum mechanics
The first C 3 ‐symmetric 44‐core‐valence‐electron triangular palladium clusters, [{(SAr′)(PAr 3 )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 [C 3 H 3 ] + , with their all‐metal aromaticity involving d‐type atomic orbitals.