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Thermal- and Photoinduced Spin-State Switching in an Unprecedented Three-Dimensional Bimetallic Coordination Polymer

Niel, Virginie
Thompson, Amber L.
Goeta, Andrés E.
Galet, Ana
Muñoz, M. Carmen
Real, José A.
Published in Chemistry - A European Journal. 2005, vol. 11, no. 7, p. 2047-2060
Abstract The compound {Fe(pmd)[Ag(CN)2][Ag2(CN)3]} (pmd=pyrimidine) was synthesized and characterized. Magnetic, calorimetric and single crystal visible spectroscopic studies demonstrate the occurrence of a two-step high-spin (HS) low-spin (LS) transition. The critical temperatures are Tc1=185 and Tc2=148 K. Each step involves 50 % of the iron centers, with the low-temperature step showing a hysteresis of 2.5 K. The enthalpy and entropy variations associated with the two steps are H1=3.6±0.4 kJ mol-1 and S1=19.5±3 J K-1 mol-1; H2=4.8±0.4 kJ mol-1 and S2=33.5±3 J K-1 mol-1. Photomagnetic and visible spectroscopy experiments show that below 50 K, where the LS state is the thermodynamically stable state, the compound can be switched quantitatively to the HS state using green-red light (550-650 nm). HS-to-LS relaxation experiments in the dark at temperatures between 15 and 55 K show that the relaxation takes place via a two-step cooperative process, which was analyzed in the context of the mean field theory. The crystal structure has been studied at 290, 220, 170, 90 and 30 K together with 30 K after irradiation. The compound adopts monoclinic symmetry (P21/c, Z=16) at all temperatures. There are five [FeN6] pseudo-octahedral sites linked by pmd, [Ag(CN)2]- and [Ag2(CN)3]- bridging ligands to form an unprecedented three-dimensional (6,6) topology. The structural analysis allows for an understanding of the microscopic mechanism of the two-step behavior of the thermally induced spin transition as well as the corresponding relaxation of the photoexcited compound based on the individual changes of the five sites. Synergy between metallophilic interactions and the spin transition is also shown by the variation of the AgAg distances. Correlations between the variation of the unit-cell volume and the change of AgAg interactions within each step with the asymmetric change of the anomalous heat capacity have also been inferred.
Keywords Argentophilic interactionsCoordination modesPolymersSpin crossover
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Research group Groupe Hauser
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NIEL, Virginie et al. Thermal- and Photoinduced Spin-State Switching in an Unprecedented Three-Dimensional Bimetallic Coordination Polymer. In: Chemistry - A European Journal, 2005, vol. 11, n° 7, p. 2047-2060. https://archive-ouverte.unige.ch/unige:3271

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Deposited on : 2009-09-21

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