Separating the racemic and meso diastereomers of a binucleating tetraphosphine ligand system through the use of nickel chloride

The reaction of a 1:1 mixture of rac- and meso-et,ph-P4 (et,ph-P4 = (Et(2)PCH(2)CH(2))(Ph)PCH(2)P(Ph)CH(2)CH(2)PEt(2)) with 2 equiv of NiCl(2).6H(2)O in EtOH produces soluble rac-Ni(2)Cl(4)(et,ph-P4) and precipitates meso-Ni(2)Cl(4)(et,ph-P4), allowing facile isolation of each bimetallic complex. Subsequent reaction with more than 250 equiv of NaCN in H(2)O/MeOH releases the et,ph-P4 ligand and Ni(CN)(4)](2-). The rac,trans- and meso,trans-Ni(CN)(2)(eta(2.5)-et,ph-P4) form as intermediates in the cyanolysis of rac- and meso-Ni(2)Cl(4)(et,ph-P4). These have been characterized by X-ray crystallography. The unusual partial isomerization of the meso- to rac-et,ph-P4 ligand via the monometallic trans-Ni(CN)(2)(eta(2.5)-et,ph-P4) intermediate complex is discussed.