A comparison of the isostructural [Co(NH3)5NO2]XNO3 and [Co(NH3)5ONO]XNO3, X = Cl- or Br- in relation to nitro-nitrito linkage isomerization and photomechanical effects.

Abstract

A new photoactive cobalt coordination compound, [Co(NH₃)₅NO₂]BrNO₃ (I), was obtained. Its crystal structure was shown to be isostructural with previously known [Co(NH₃)₅NO₂]ClNO₃ (II) for which linkage isomerization accompanied with mechanical response of the crystal has been already reported. Single crystals of I are transformed into nitrito isomer [Co(NH₃)₅ONO]BrNO₃ (III) on irradiation with blue light (λ = 465 nm) without being destroyed. The crystal structure of III was also solved using single-crystal X-ray diffraction and compared with previously known [Co(NH₃)₅ONO]ClNO₃ (IV). A detailed comparison of the structures of I, II, III and IV, including unit-cell parameters, the distribution of free space (in particular, reaction cavities around the nitro ligand), the lengths of hydrogen bonds, coordination and Voronoi-Dirichlet polyhedra has been performed. Single-crystal X-ray diffraction data were complemented with IR spectra. The effect of the replacement of Cl^- by Br^- on the crystal structure and on the nitro-nitrito photoisomerization is discussed.