An electron rich “hybrid” asymmetric aminophosphine, (diisopropylamino)(morpholino) (phenyl)phosphine, L, was synthesized in good yield by step‐wise aminolysis reactions with dichloro(phenyl)phosphine and structurally characterized. The complex, CuCl(L) was readily isolated from both 1∶1 and 1∶2 reactions of L with CuCl. Single crystal X‐ray structures of L and two copper complexes, [CuCl(L) · CH3CN]2 (1) and [CuCl(L) · CH2Cl2]2 (2) have been determined. X‐ray structures reveal pyramidal nature of phosphorus and near planar geometry of nitrogen of the phosphine ligand and the dimeric nature of the complexes with tricoordinate copper(I) centers. The asymmetric phosphine crystallizes in monoclinic system with space group P21/c and unit cell dimensions as a=17.219(1) Å, b=13.469(1) Å, c=7.395(5) Å, α=90.00°, β=93.11(1)°, γ=90.00°. Both acetonitrile (1) and dichloromethane (2) solvates crystallize in triclinic system with space group Pī. The unit cell dimensions of (1) are a=10.143(2) Å, b=13.681(3) Å, c=16.647(3) Å, α=83.14(1)°, β=76.91(1)°, γ=68.83(1)° and that of (2) are a=8.899(1) Å, b=11.727(1) Å, c=11.784(1) Å. α=66.73(1)°, β=82.27(1)°, γ=84.04(1)°. This is the first report of copper(I) phosphine complexes in which the coordinated asymmetric phosphine carries two different amino substituents.
Read full abstract