Comparison of mol­ecular structures of cis-bis­[8-(di­methyl­phosphan­yl)quinoline]­nickel(II) and -platinum(II) complex cations

The crystal structures of the complexes (SP-4-2)-cis-bis­[8-(di­methyl­phosphan­yl)quinoline-κ(2) N,P]nickel(II) bis­(perchlorate) nitro­methane monosolvate, [Ni(C(11)H(12)NP)(2)](ClO(4))(2)·CH(3)NO(2) (1), and (SP-4-2)-cis-bis­[8-(di­methyl­phos­phan­yl)quinoline-κ(2) N,P]platinum(II) bis­(tetra­fluoro­borate) aceto­nitrile monosolvate, [Pt(C(11)H(12)NP)(2)](BF(4))(2)·C(2)H(3)N (2), are reported. In both complex cations, two phosphanyl­quinolines act as bidentate P,N-donating chelate ligands and form the mutually cis configuration in the square-planar coordination geometry. The strong trans influence of the di­methyl­phosphanyl donor group is confirmed by the Ni—N bond lengths in 1, 1.970 (2) and 1.982 (2) Å and, the Pt—N bond lengths of 2, 2.123 (4) and 2.132 (4) Å, which are relatively long as compared to those in the analogous 8-(di­phenyl­phosphan­yl)quinoline complexes. Mutually cis-positioned quinoline donor groups would give a severe steric hindrance between their ortho-H atoms. In order to reduce such a steric congestion, the Ni(II) complex in 1 shows a tetra­hedral distortion of the coordination geometry, as parameterized by τ(4) = 0.199 (1)°, while the Pt(II) complex in 2 exhibits a typical square-planar coordination geometry [τ(4) = 0.014 (1)°] with a large bending deformation of the ideally planar Me(2)Pqn chelate planes. In the crystal structure of 2, three F atoms of one of the BF(4) (−) anions are disordered over two sets of positions with refined occupancies of 0.573 (10) and 0.427 (10).