z-logo
Premium
Synthesis and characterization of μ‐oxamido copper(II)‐iron(II) heterobinuclear complexes with an antiferromagnetic exchange interaction
Author(s) -
Yan CuiWei,
Li YanTuan,
Liao DaiZheng
Publication year - 1997
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.19970150604
Subject(s) - chemistry , antiferromagnetism , molar conductivity , copper , crystallography , octahedron , magnetic susceptibility , metal , ion , magnetic moment , exchange interaction , inorganic chemistry , condensed matter physics , crystal structure , ferromagnetism , physics , organic chemistry
Four new μ‐oxamido heterobinuclear complexes have been synthesized and identified as [Cu(oxap)Fe(L) 2 ]SO 4 , where oxap denotes the N , N' ‐bis(2‐aminopropyl)oxamido dianion and L represents diaminoethane (en); 1,3‐diaminopropane (pn); 1,2‐diaminopropane (ap) and 2,9‐dimethyl‐l,10‐phenanthroline (Me 2 ‐phen). Based on the elemental analyses, spectroscopic studies, magnetic moments (at room temperature) and molar conductivity measurements, extended oxamido‐bridged structures consisting of a copper(II) and an iron(II) ions, which have a square planar environment and an octahedral environment, respectively, are proposed for these complexes. Complexes [Cu(oxap)Fe(en) 2 ]SO 4 (1) and [Cu(oxap)Fe(pn) 2 ]SO 4 (2) have been characterized by variable temperature magnetic susceptibility (4.2∼'300 K) and the observed data were least‐squares fitted to the susceptibility equation derived from the spin Hamiltonian including single‐ion aero‐field interaction for the iron(II) ion, H =−2JŜ 1 ·;Ŝ 2 — D Ŝ 2 zl , giving the exchange integrals J =−21.9 cm −1 for 1 and J =−23.6 cm −1 for 2. These results are commensurate with antiferromagnetic interactions between adjacent metal ions within each molecule.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here