A monometallic Rh(III) tetraphosphine complex: Reductive activation of CH2Cl2 and selective meso to racemic tetraphosphine ligand isomerization

The first Rh complex with an eta (4)-coordinated rac-et,ph-P4 ligand [et,ph -P4 = (Et2PCH2CH2)(Ph)PCH2P(Ph)(CH2CH2PEt2)] has been synthesized by reacti ng [Rh(nbd)(2)]BF4 with meso- or rac-et,ph-P4 in dichloromethane. The react ion occurs fairly rapidly at room temperature to form [rac-RhCl2(eta (4)-et ,ph-P4)](+) in high yields, regardless of whether one starts with mixed or even pure meso-et,ph-P4 ligand. This unusual and highly selective metal ass isted isomerization of the meso-et,ph-P4 ligand to its rac-et,ph-P4 disaste reomer will be discussed.