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Versatility of iron(III) upon coordination with the binucleating ligand N,N′-bis-(2-hydroxy, 3-carboxybenzilidene)1,2-diaminoethane

✍ Scribed by J. Zarembowitch; O. Kahn; J. Jaud; J. Galy


Publisher
Elsevier Science
Year
1982
Tongue
English
Weight
199 KB
Volume
65
Category
Article
ISSN
0020-1693

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✦ Synopsis


Strictly speakmg, the symmetry of the FeOe chromophore is below axial and a rhombic zero field splitting parameter E should be introduced in the spin Hamiltonian. In other respects, the intermolecular interactions, that we did not take into account, are most probably very weak owing to the large separation between the complex cations. **The X-band powder E.P.R. spectra for both A and B at 4 K exhibit very broad peaks (4000 G) centered at 1730 G and 2000 G respectively.


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The crystal structure of a copper(II) complex of 2acetylpyridine 3-piperidylthiosemicarbazone, [Cu(Acpip) 2 ], indicates a tridentate, monoanionic ligand (i. e., pyridine nitrogen, imine nitrogen and thiolato sulfur atoms) and a bidentate, monanionic ligand (i. e., imine nitrogen and thiolato sulfur