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   <subfield code="a">Spin-crossover complexes in solution, I. Substitutional lability of [Fe( bzimpy )2](ClO4)2</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Bernhard Strauß, Wolfgang Linert, Viktor Gutmann, Reginald Jameson]</subfield>
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   <subfield code="a">Spin-crossover-Komplexe in Lösung, 1. Mitt.: Substitutionslabilität von [Fe( bzimpy )2](ClO4)2</subfield>
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   <subfield code="a">Summary: The iron(II) complexes of the nitrogen donor ligand 2,6-bis(benzimidazol-2′-yl)pyridine (bzimpy) have been investigated in nonaqueous solvents using various spectrophotometric methods. Measurements in methanol at 20°C revealed thatbzimpy can act as a bi-or tridendate ligand towards iron(II) in this solvent, forming [Fe(bzimpy)]2+ (tridendate, logK=5.54), [Fe(bzimpy)2]2+ (bistridentate, logK=4.12) and [Fe(bzimpy)3]2+ (tris-bidentate, logK=3.85). The pronounced thermochromism of the compound is shown to be the result of both spin-crossover and dissociation equilibria. Furthermore, in solvents of higher donor numbers (≥30), partial or complete deprotonation of the complex [Fe(bzimpy)3]2+ is observed. Triethylamine added stepwise to methanolic solutions causes successive deprotonation.</subfield>
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   <subfield code="a">Deprotonation</subfield>
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   <subfield code="t">Monatshefte für Chemie / Chemical Monthly</subfield>
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