Investigation of nitro–nitrito photoisomerization: crystal structures of trans-{2,2′-[ethane-1,2-diylbis(nitrilo­methyl­idyne)]diphenolato}(pyridine/4-methyl­pyridine)­nitro­cobalt(III)

摘要

The reaction cavities of the nitro groups in the title compounds, trans-{2,2′-[ethane-1,2-diylbis(nitrilo­methyl­idyne)]diphenolato-κ4O,N,N′,O′}(nitro-κN)(pyridine-κN)cobalt(III), [Co(C16H14N2O2)(NO2)(C5H5N)], (I), and trans-{2,2′-[ethane-1,2-diylbis(nitrilo­methyl­idyne)]diphenolato-κ4O,N,N′,O′}(4-methyl­pyridine-κN)(nitro-κN)cobalt(III), [Co(C16H14N2O2)(NO2)(C6H7N)], (II), have been investigated to reveal that the inter­molecular CMe—H⋯O(nitro) contacts in (II) are unfeasible for the nitro–nitrito photochemical linkage isomerization process. In (I), there are two independent complexes showing similar conformations, and the central five-membered chelate ring of the tetra­dentate salen ligand adopts the same absolute configuration. This is the result of pseudo-spontaneous resolution, since the configuration of the five-membered chelate ring may frequently be reversed in solution. In the crystals of (I) and (II), the mol­ecules are linked into three-dimensional networks by C—H⋯O hydrogen bonds.