FeIII in the high-spin state in dimethylammonium bis[3-ethoxysalicylaldehyde thiosemicarbazonato(2-)-κ3O2,N1,S]ferrate(III)
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Updated: Aug 15, 2025

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
Robyn E Powell1, Martin R Lees2, Graham J Tizzard3
1College of Engineering and Physical Sciences, School of Infrastructure and Sustainable Engineering, Department of Chemical Engineering and Applied Chemistry, Aston University, Aston Triangle, Birmingham, West Midlands, B4 7ET, United Kingdom.
Abstract:
The synthesis and crystal structure (100 K) of the title compound, [(CH3)2NH2][Fe(C10H11O2N3S)2], are reported. The asymmetric unit consists of an octahedral [FeIII(L)2]- fragment, where L2- is 3-ethoxysalicylaldehyde thiosemicarbazonate(2-), and a dimethylammonium cation. Each L2- ligand binds with the thiolate S, the imine N and the phenolate O atoms as donors, resulting in an FeIIIS2N2O2 chromophore. The ligands are orientated in two perpendicular planes, with the O and S atoms in cis positions, and mutually trans N atoms. The FeIII ion is in the high-spin state at 100 K. The variable-temperature magnetic susceptibility measurements (5-320 K) are consistent with the presence of a high-spin FeIII ion with D = 0.83 (1) cm-1 and g = 2.
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