Controlled Intramolecular Electron Transfers in Cyanide-Bridged Molecular Squares by Chemical Modifications and External Stimuli

A series of cyanide bridged Fe-Co molecular squares, [Co2Fe2(CN)(6)(tp*)(2)(dtbbpy)(4)](PF6)(2)center dot 2MeOH (1), [Co2Fe2(CN)(6)(tp*)(2)(bpy)(4)](PF6)(2)center dot 2MeOH (2), and [Co2Fe2(CN)(6)(tp)(2)(dtbbpy)(4)](PF6)(2)center dot 4H(2)O (3) (tp = hydrotris(pyrazol-1-yl)borate, tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate, bpy =2,2`-bipyridine, dtbbpy =4,4`-di-tert-butyl-2,2`-bipyridine), were prepared by the reactions of [Fe(CN)(3)(L)](-) (L = tp or tp*) with Co2+ and bidentate ligands (bpy or dtbbpy) in MeOH. In the molecular squares, Fe and Co ions are alternately bridged by cyanide ions, forming macrocyclic tetranuclear cores. Variable temperature X-ray structural analyses and magnetic susceptibility measurements confirmed that 1 exhibits two-step charge-transfer induced spin transitions (CTIST) centered at T-1/2 = 275 and 310K in the solid state. The Fe and Co ions in 1 are the low-spin (LS) Fe(III) and high-spin (HS) Co(II) ions, described here in the high-temperature (HT) phase ([(FeLS2CoHS2II)-Co-III]) at 330 K, while a low-temperature (LT) phase ([(FeLS2CoLS2III)-Co-II]) with LS Fe(II) and Co(III) ions was dominant below 260 K. X-ray structural analysis revealed that in the intermediate (IM) phase at 298 K 1 exhibits positional ordering of [(FeLS2CoHS2II)-Co-III] and [(FeLS2CoLS2III)-Co-II] species with the 2:2 ratio. In photomagnetic experiments on 1, light-induced CTIST from the LT to the HT phase was observed by excitation of Fe(II) -> Co(III) intervalence charge transfer (IVCT) band at 5 K and the trapped HT phase thermally relaxed to the LT phase in a two-step fashion. On the other hand, 2 and 3 are in the HT and LT phases, respectively, throughout the entire temperature range measured, and no CTIST was observed. UV-vis-NIR absorption spectral measurements and cyclic voltammetry in solution revealed that the different electronic states in 1-3 are ascribable to the destabilization of iron and cobalt ion d-orbitals by the introduction of methyl and tert-butyl groups to the ligands tp and bpy, respectively. Temperature dependence of UV-vis-NIR spectra confirmed that 1 exhibited a one-step CTIST in butyronitrile, of which T-1/2 varied from 227 to 280 K upon the addition of trifluoroacetic acid.