Synthesis, Solid-State Structure, Magnetic Properties and Mössbauer Spectral Studies of {Fe[HC(3,5-Me₂pz)₃](H₂O)₃} (BF₄)₂
Abstract
The reaction of Fe(BF4)2·6H2O and one equivalent of HC(3,5-Me2pz)3 in acetonitrile leads to the formation of {Fe[HC(3,5-Me2pz)3](H2O)3} (BF4)2. The solution phase 1H NMR spectrum is broad with chemical shifts ranging from 54 to -42 ppm, a range that is indicative of a paramagnetic high-spin complex. Magnetic moment measurements show that the complex is paramagnetic in the solid-state with μeff = 4.89μB. The solid-state structure shows the N3FeO3 central core is a distorted octahedron with N-Fe-N angles averaging 84.4° and O-Fe-O angles averaging 90.0°. The average Fe-N distance is 2.18 Å and the average Fe-O bond distance is 2.12 Å. Mössbauer spectra, obtained at 78 and 295 K, clearly reveal that this complex is high-spin at these temperatures with hyperfine parameters typical of a pseudooctahedral iron(II) complex.
Recommended Citation
D. L. Reger et al., "Synthesis, Solid-State Structure, Magnetic Properties and Mössbauer Spectral Studies of {Fe[HC(3,5-Me₂pz)₃](H₂O)₃} (BF₄)₂," Inorganica Chimica Acta, vol. 316, no. 1-2, pp. 65 - 70, Elsevier Limited, May 2001.
The definitive version is available at https://doi.org/10.1016/S0020-1693(01)00381-4
Department(s)
Chemistry
Keywords and Phrases
Acetonitrile; Iron Complex; Lead; Nitrogen; Oxygen; Crystal Structure; Crystallography; Drug Synthesis; Magnetism; Mössbauer Spectroscopy; Proton Nuclear Magnetic Resonance; Radiation; Solid State; Temperature; Mössbauer; Pyrazolylmethane Complexes
International Standard Serial Number (ISSN)
0020-1693
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2001 Elsevier Limited, All rights reserved.
Publication Date
01 May 2001