A Pyrazolate-Supported Fe3(μ3-O) Core: Structural, Spectroscopic, Electrochemical, and Magnetic Study
Inorganic Chemistry2007Vol. 46(26), pp. 10981–10989
Citations Over TimeTop 11% of 2007 papers
D.M. Pinero, P. Baran, Roman Boča, Radovan Herchel, Michael Klein, Raphael G. Raptis, Franz Renz, Yiannis Sanakis
Abstract
A comparison is made between the structural, spectroscopic, electrochemical, and magnetic properties of pyrazolate versus carboxylate complexes [Fe3(mu3(mu3O)(mu-LL)6Cl3]2- containing the Fe3(mu3-O)-motif. While the Fe3(mu3-O)-cores are structurally indistinguishable in the two types of complexes, their magnetic properties deviate from the expected values as a result of a through-pyrazole contribution to the overall antiferromagnetic exchange with J1/hc = -80.1 cm(-1) and J2/hc = -72.4 cm(-1), or J1/hc = 70.6 cm(-1) and J2/hc = -80.8 cm(-1), (Hex = -J1(S1S2 + S2S3) - J2S1S3). The magnetic properties of the pyrazolate complexes are further tuned by an antisymmetric exchange interaction term.
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