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Magnetic Ordering in Iron(II) Complexes due to a 2D Network of Hydrogen Bonds
Author(s) -
Weber Birgit,
Jäger ErnstG.
Publication year - 2009
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.200800338
Subject(s) - schiff base , octahedron , hydrogen bond , ligand (biochemistry) , crystallography , chemistry , methanol , magnetic susceptibility , magnetization , stereochemistry , crystal structure , molecule , physics , organic chemistry , receptor , biochemistry , quantum mechanics , magnetic field
The magnetic properties of two octahedral iron(II) complexes with Schiff base like equatorial N 2 O 2 coordinating ligands and methanol (MeOH) as axial ligand are reported. Both compounds [FeL1(MeOH) 2 ] ( 1 ) and [FeL2(MeOH) 2 ] ( 2 ) (with L1 = [3,3′]‐[1,2‐phenylenebis(iminomethylidyne)‐bis(2,4‐pentanedionato)(2‐)‐N,N′,O 2 ,O 2 ′] and L2 = [E,E]‐[{diethyl 2,2′‐1,2‐phenylenebis(iminomethylidyne)bis(3‐oxo‐3‐phenylpropanato)} (2‐)‐N,N′,O3,O3′]) show a weak spontaneous magnetization below T C = 10 K. Results from X‐ray structure analysis of 1 indicate, that this is due to 2D network of hydrogen bonds as previously discussed for a similar complex.

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