Abstract
The reaction of Fe(BF 4 ) 2 ·6H 2 O and one equivalent of HC(3,5-Me 2 pz) 3 in acetonitrile leads to the formation of {Fe[HC(3,5-Me 2 pz) 3 ](H 2 O) 3 } (BF 4 ) 2 . The solution phase 1 H 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 μ eff = 4.89μ B . The solid-state structure shows the N 3 FeO 3 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.
| Original language | American English |
|---|---|
| Journal | Inorganica Chimica Acta |
| Volume | 316 |
| DOIs | |
| State | Published - May 1 2001 |
Keywords
- Acetonitrile
- Crystal Structure
- Crystallography
- Drug Synthesis
- Iron Complex
- Lead
- Magnetism
- Mössbauer
- Mössbauer Spectroscopy
- Nitrogen
- Oxygen
- Proton Nuclear Magnetic Resonance
- Pyrazolylmethane Complexes
- Radiation
- Solid State
- Temperature
Disciplines
- Chemistry
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