Abstract
Phenylene-1,2-bis(phosphane) reacts with two mole-equivalents of tris[(triphenylphosphane)gold(I)]oxonium tetrafluoroborate in dichloromethane at -78°C to give high yields of a hexanuclear complex (C6H4[P(AuPPh3)3]2] 2+ · 2 BF4- (1). The variable-temperature 31P{1H}-NMR spectra of the product in CD2Cl2 at -80°C are compatible with a static structure featuring three Ph3PAu units associated with each of the two C6H4P2 phosphide functions, as derived from a clear doublet/quartet pattern. At 50°C in CDCl3, however, there is rapid intramolecular scrambling of these Ph3PAu units, which gives rise to a triplet/septet pattern with the J(P,P) value reduced to exactly one half of the value at the low-temperature limit.
Original language | English |
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Pages (from-to) | 217-219 |
Number of pages | 3 |
Journal | Chemische Berichte |
Volume | 130 |
Issue number | 2 |
DOIs | |
State | Published - 1997 |
Keywords
- (Phosphane)gold(i) complexes
- Clusters
- Gold compounds
- P Ligands