A new ferrimagnetically ordered charge-transfer complex based on high-spin iron(III) chelate tetracyanoethenide with a Tc of 10 K

The reaction of the high-spin iron(II) quadridentate chelate complex [Fe(L)], (L=diethyl( E, E)-2,2′-[1,2-phenylenebis-(iminomethylidyne)]-bis-[3-oxobutanoate]), with the electron acceptor tetracyanoethylene (TCNE) leads to the formation of the 1:1 charge-transfer (CT) complex [Fe(L)] +[TCNE] −. The...

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Bibliographic Details
Published inJournal of magnetism and magnetic materials Vol. 246; no. 1; pp. 283 - 289
Main Authors Müller, Bernd R., Leibeling, Guido, Jäger, Ernst-G.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.04.2002
Elsevier Science
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Summary:The reaction of the high-spin iron(II) quadridentate chelate complex [Fe(L)], (L=diethyl( E, E)-2,2′-[1,2-phenylenebis-(iminomethylidyne)]-bis-[3-oxobutanoate]), with the electron acceptor tetracyanoethylene (TCNE) leads to the formation of the 1:1 charge-transfer (CT) complex [Fe(L)] +[TCNE] −. The magnetic characterisation of the CT salt indicates a chain structure with alternating S= 5 2 high-spin iron(III) and S= 1 2 TCNE − radicals in which the spin centres are antiferromagnetic correlated. The antiferromagnetic intrachain interaction parameter is very weak ( J intra≈−8 cm −1) based on the spin Hamiltonian H=−J intra S i S j . At T=2 K and H=5.5 kG the magnetisation for the CT complex is about 83% of the saturation magnetisation value expected for a S total =( 5 2 − 1 2 )=2 system. A magnetic hysteresis loop was observed at T=2 K with a coercive field of 200 G. Below 10 K, the complex shows a weak spontaneous magnetisation characteristic for a canted ferrimagnet.
ISSN:0304-8853
DOI:10.1016/S0304-8853(02)00075-6