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The complete mol­ecule of the title complex, [Cu2(C13H19N2O2)2(N3)2], is generated by the application of a centre of inversion. The central Cu2N2 core is a rhombus as the μ2-azide ligands bridge in an asymmetric fashion. Each CuII atom is also coordinated by a monoanionic tridentate Schiff base ligand via the anti­cipated oxide O, imine N and amine N atoms. The resulting N4O coordination geometry is based on a square pyramid. No specific inter­molecular inter­actions are noted in the crystal packing, but the amine H atoms form intra­molecular N—H...O(oxide)/N(azide) hydrogen bonds.

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Two distinct coordination geometries are found in the binuclear title complex, [Ni2(C13H19N2O2)2(N3)2(CH3OH)], as one Schiff base ligand is penta­dentate, coordinating via the anti­cipated oxide O, imine N and amine N atoms (as for the second, tridentate, ligand) but the oxide O is bridging and coordination also occurs through the meth­oxy O atom. The NiII atoms are linked by a μ2-oxide atom and one end of a μ2-azide ligand, forming an Ni2ON core. The coordination geometry for the NiII atom coordinated by the tridentate ligand is completed by the meth­oxy O atom derived from the penta­dentate ligand, with the resulting N3O3 donor set defining a fac octa­hedron. The second NiII atom has its cis-octa­hedral N4O2 coordination geometry completed by the imine N and amine N atoms of the penta­dentate Schiff base ligand, a terminally coordinated azide N and a methanol O atom. The arrangement is stabilized by an intra­molecular hydrogen bond between the methanol H and the oxide O atom. Linear supra­molecular chains along the a axis are formed in the crystal packing whereby two amine H atoms from different amine atoms hydrogen bond to the terminal N atom of the monodentate azide ligand.
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