Effects of N-oxidation on the molecular and crystal structures and properties of isocinchomeronic acid, its metal complexes and their supramolecular architectures: experimental, CSD survey, solution and theoretical approaches

摘要

Nine coordination complexes and polymer (M/L/X) based on Co, Ni, Zn, Cu (M), pyridine-N-oxide-2,5-dicarboxylic acid (H(2)pydco) (L) and either isonicotinamide (Ina), piperazine (pipz), 2,2 '-bipyridine (bipy) and 1,10-phenanthroline (phen) (X) were synthesized and characterized by elemental analyses, infrared spectroscopy and single crystal X-ray diffraction. The resulting empirical formulae of the prepared complexes are [Co(H2O)(6)][Co(pydco)(2)(H2O)(2)]center dot 2H(2)O (1), [M(pydco)(H2O)(4)](2) [M = Co (2), Ni (3), Zn (4)], [Co(pydco)(bipy)(H2O)(2)]center dot 4H(2)O (5), [Co(pydco)(phen)(H2O)(2)]center dot 5.135(H2O)center dot 0.18(EtOH) (6), [Cu(Hpydco)(bipy)Cl]center dot 2H(2)O (7), [Cu(Hpydco)(bipy)Cl](2)center dot 2H(2)O (8), and {[AgCu(H2O)(2)(phen)(pydco)]NO3}(n) (9). With the exception of 9, which forms an extended structure via multiple coordination modes, all the complexes contain (H)pydco as a bidentate ligand coordinated to the metal ion via the N-oxide and the adjacent carboxylate group oxygen atom, creating a chelate ring. The metal centers exhibit either distorted octahedral (1-6) or square pyramidal (7-9) geometry. Our results demonstrate that, when acting cooperatively, non-covalent interactions such as X-HMIDLINE HORIZONTAL ELLIPSISO hydrogen bonds (X = O, N, C), C-OMIDLINE HORIZONTAL ELLIPSIS pi and pi MIDLINE HORIZONTAL ELLIPSIS pi stacking represent driving forces for the selection of different three-dimensional structures. Moreover, in compounds 2-4, 1D supramolecular chains are formed where OMIDLINE HORIZONTAL ELLIPSIS pi-hole interactions are established, which unexpectedly involve the non-coordinated carboxylate group. The non-covalent interaction (NCI) plot index analysis reveals the existence of the OMIDLINE HORIZONTAL ELLIPSIS pi-hole interactions that have been evaluated using DFT calculations. The Cremer and Pople ring puckering parameters are also investigated. The complexation reactions of these molecules with M were investigated by solution studies. The stoichiometry of the most abundant species in the solution was very close to the corresponding crystals. Finally, the effect of N-oxidation on the geometry of complexes has been also studied using the Cambridge Structural Database. It shows that complexes containing N-oxidized H(2)pydc are very rare.