A mononuclear FeII complex, prepared with a Brønsted diacid ligand, H2 L (H2 L=2-[5-phenyl-1H-pyrazole-3-yl] 6-benzimidazole pyridine), shows switchable physical properties and was isolated in five different electronic states. The spin crossover (SCO) complex, [FeII (H2 L)2 ](BF4 )2 (1A ), exhibits abrupt spin transition at T1/2 =258 K, and treatment with base yields a deprotonated analogue [FeII (HL)2 ] (1B ), which shows gradual SCO above 350 K. A range of FeIII analogues were also characterized. [FeIII (HL)(H2 L)](BF4 )Cl (1C ) has an S=5/2 spin state, while the deprotonated complexes [FeIII (L)(HL)], (1D ), and (TEA)[FeIII (L)2 ], (1E ) exist in the low-spin S=1/2 state. The electronic properties of the five complexes were fully characterized and we demonstrate in situ switching between multiple states in both solution and the solid-state. The versatility of this simple mononuclear system illustrates how proton donor/acceptor ligands can vastly increase the range of accessible states in switchable molecular devices.
Keywords: Brønsted acid/base; iron; magnetism; molecular switch; spin crossover.
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