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Three iron(II) complexes, [Fe(TPMA)(BIM)](ClO(4))(2)⋅0.5H(2)O (1), [Fe(TPMA)(XBIM)](ClO(4))(2) (2), and [Fe(TPMA)(XBBIM)](ClO(4))(2)⋅0.75CH(3)OH (3), were prepared by reactions of Fe(II) perchlorate and the corresponding ligands (TPMA=tris(2-pyridylmethyl)amine, BIM=2,2'-biimidazole, XBIM=1,1'-(α,α'-o-xylyl)-2,2'-biimidazole, XBBIM=1,1'-(α,α'-o-xylyl)-2,2'-bibenzimidazole). The compounds were investigated by a combination of X-ray crystallography, magnetic and photomagnetic measurements, and Mössbauer and optical absorption spectroscopy. Complex 1 exhibits a gradual spin crossover (SCO) with T(1/2) =190 K, whereas 2 exhibits an abrupt SCO with approximately 7 K thermal hysteresis (T(1/2) =196 K on cooling and 203 K on heating). Complex 3 is in the high-spin state in the 2-300 K range. The difference in the magnetic behavior was traced to differences between the inter- and intramolecular interactions in 1 and 2. The crystal packing of 2 features a hierarchy of intermolecular interactions that result in increased cooperativity and abruptness of the spin transition. In 3, steric repulsion between H atoms of one of the pyridyl substituents of TPMA and one of the benzene rings of XBBIM results in a strong distortion of the Fe(II) coordination environment, which stabilizes the high-spin state of the complex. Both 1 and 2 exhibit a photoinduced low-spin to high-spin transition (LIESST effect) at 5 K. The difference in the character of intermolecular interactions of 1 and 2 also manifests in the kinetics of the decay of the photoinduced high-spin state. For 1, the decay rate constant follows the single-exponential law, whereas for 2 it is a stretched exponential, reflecting the hierarchical nature of intermolecular contacts. The structural parameters of the photoinduced high-spin state at 50 K are similar to those determined for the high-spin state at 295 K. This study shows that N-alkylation of BIM has a negligible effect on the ligand field strength. Therefore, the combination of TPMA and BIM offers a promising ligand platform for the design of functionalized SCO complexes.
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http://dx.doi.org/10.1002/chem.201202045 | DOI Listing |
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