Thermal and light-induced spin-crossover in salts of the heptadentate complex [tris(4-{pyrazol-3-yl}-3-aza-3-butenyl)amine]iron(ii) |
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Authors: | Lazar Hanane Z Forestier Thibaut Barrett Simon A Kilner Colin A Létard Jean-François Halcrow Malcolm A |
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Institution: | Institut de Chimie de la Matière Condensée de Bordeaux, UPR CNRS 9048 - Université de Bordeaux 1, Groupe des Sciences Moléculaires, 87 Av. Doc. A. Schweitzer, F-33608 Pessac, France. |
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Abstract: | The syntheses of FeL]BF(4)](2).H(2)O, FeL]ClO(4)](2).H(2)O, FeL]NO(3)](2).CH(3)NO(2) and FeL]CF(3)SO(3)](2) (L = tris(4-{pyrazol-3-yl}-3-aza-3-butenyl)amine) are described. The isostructural BF(4)(-) and ClO(4)(-) salts are high-spin between 5-300 K, while the other two compounds are high-spin at room temperature but undergo gradual high-->low spin transitions upon cooling. For FeL]NO(3)](2) this transition is centred at 139 K and proceeds to near-completeness, while for FeL]CF(3)SO(3)](2) it is centred at 144 K and only proceeds to 50% conversion. The CF(3)SO(3)(-) salt also undergoes spin-crossover centred at 200 K in (CD(3))(2)CO solution, and exhibits dynamic inversion of its helical ligand conformation. All these compounds except the triflate salt have been crystallographically characterised, and show capped trigonal antiprismatic 6 + 1] coordination geometries. The NO(3)(-) and CF(3)SO(3)(-) salts undergo quantitative conversion to trapped, high-spin excited states upon irradiation with a green laser at 10 K (the LIESST effect; LIESST = Light-Induced Excited Spin State Trapping). The thermal stabilities of their LIESST excited states (T(LIESST) = 80-82 K) resemble those found for iron(ii) complexes of bidentate N-heterocyclic ligands. Hence, the LIESST properties of FeL](2+) are those of a complex of three rigid bidentate domains linked by a flexible spacer, rather than of a single encapsulating podand. |
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