Abstract
The asymmetric unit of the solvated title complex, [Ir(C(11)H(8)N)(2)(C(15)H(14)NO(3))]·2CH(2)Cl(2), consists of two complex mol-ecules together with four di-chloro-methane solvent mol-ecules, one of which is disordered. In each complex mol-ecule, the Ir(III) ion has a distorted octa-hedral coordination environment defined by two 2-phenyl-pyridine ligands, through two phenyl C and two pyridine N atoms, and by one N,O-bidentate 2-[(2,4-di-meth-oxy-phenyl-imino)-meth-yl]phenolate anion. The Ir(III) ions lie almost in the equatorial planes with deviations of 0.0396 (17) and 0.0237 (17) Å, respectively, for the two complex mol-ecules. In both complex mol-ecules, the two 2-phenyl-pyridine ligands are nearly perpendicular to each other [dihedral angles between the least-squares-planes of 89.91 (11) and 85.13 (11)°]. In the crystal, inter-molecular C-H⋯O inter-actions as well as inter-molecular C-H⋯π inter-actions are present, leading to a three-dimensional network structure. One of the four dichlormethane solvent mol-ecules shows disorder over two sets of sites [occupancy ratio 0.79 (2):0.21 (2)].