A. Jouaiti et al., MONO-DENTATE AND BI-DENTATE PHOSPHAALKENE LIGANDS - STRUCTURES OF THEIR COPPER(I) CHLORIDE COMPLEXES, Journal of the Chemical Society. Dalton transactions, (11), 1994, pp. 1685-1688
While the reaction of the monophosphaalkene -tri-tert-butylphenyl)phos
phanediylmethyl]-benzene (L2) with copper(I) chloride ed to a dimeric
complex [Cu2Cl2L22(NCMe)2] 1, use of the diphosphaalkene 6-tri-tert-bu
tylphenyl)phosphanediylmethyl]benzene (L1) gave rise to a tetrameric c
omplex [Cu4Cl4L12].3EtOH 2. The crystal structures of the complexes ha
ve been determined and indicate that 1 is a centrosymmetric dimer with
tetrahedrally co-ordinated copper(I) centres, whereas 2 adopts a 'cub
ane-like' structure with pairs of copper atoms bridged by different L1
units.