Spin Crossover in Fe(II)–M(II) Cyanoheterobimetallic Frameworks (M = Ni, Pd, Pt) with 2-Substituted Pyrazines
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文摘
Discovery of spin-crossover (SCO) behavior in the family of FeII-based Hofmann clathrates has led to a “new rush” in the field of bistable molecular materials. To date this class of SCO complexes is represented by several dozens of individual compounds, and areas of their potential application steadily increase. Starting from Fe2+, square planar tetracyanometalates MII(CN)42– (MII = Ni, Pd, Pt) and 2-substituted pyrazines Xpz (X = Cl, Me, I) as coligands we obtained a series of nine new Hofmann clathrate-like coordination frameworks. X-ray diffraction reveals that in these complexes FeII ion has a pseudo-octahedral coordination environment supported by four μ4-tetracyanometallates forming its equatorial coordination environment. Depending on the nature of X and M, axial positions are occupied by two 2X-pyrazines (X = Cl and MII = Ni (1), Pd (2), Pt (3); X = Me and MII = Ni (4), Pd (5)) or one 2X-pyrazine and one water molecule (X = I and MII = Ni (7), Pd (8), Pt (9)), or, alternatively, two distinct FeII positions with either two pyrazines or two water molecules (X = Me and MII = Pt (6)) are observed. Temperature behavior of magnetic susceptibility indicates that all compounds bearing FeN6 units (16) display cooperative spin transition, while FeII ions in N5O or N4O2 surrounding are high spin (HS). Structural changes in the nearest FeII environment upon low-spin (LS) to HS transition, which include ca. 10% Fe–N distance increase, lead to the cell expansion. Mössbauer spectroscopy is used to characterize the spin state of all HS, LS, and intermediate phases of 19 (see abstract figure). Effects of a pyrazine substituent and MII nature on the hyperfine parameters in both spin states are established.

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