Structural variety and stereochemical features of bis(diphenylphosphinyl)[3]ferrocenophane gold(I) complexes

The P,N-[3]ferrocenophane ligand 3 forms a (κP-ligand)AuCl complex (5) upon treatment with (Me2S)AuCl. The corresponding P,P-[3]ferrocenophane system 4 yields a binuclear (κP,κP-chelate ligand)(AuCl)2 complex (6) when reacted with 2 equivalents of the (Me2S)AuCl reagent. Complex 6 features an intramolecular aurophilic Au⋯Au interaction. Treatment of the P,P-[3]ferrocenophane 4 with 1.0 equiv. of (PPh3)AuCl gives the tetra-coordinated mono-gold(I) complex (P,P-ligand)(PPh3)AuCl (7), whereas the cationic [(P,P-ligand)2Au]+[Cl−] system is obtained from 4 and 0.5 equivalents of (Me2S)AuCl. The [(P,P-ligand)2Au]+ system is obtained in different diastereoisomeric forms (8 and 9) depending on the stereochemistry of the pair of P,P-[3]ferrocenophane chelate ligand used. Examples of the complexes 5, 6, 7 and 8 were characterized by X-ray diffraction.

The [3]ferrocenophane derived P,P-chelate ligands react with (Me2S)AuCl in a 2:1 stoichiometry to yield the chiral [bis-ligandAu+]Cl− complexes (8 and 9).Figure optionsDownload as PowerPoint slideResearch highlights
► Gold complexes of ferrocenophane based bidentate ligands are prepared.
► The stereochemistry of cationic bis(chelate)ligand gold complexes is investigated.
► Aurophilic interaction at bis-phosphino-ferrocenophane di-gold complexes is characterized.