Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1340763 | Polyhedron | 2007 | 9 Pages |
We report the X-ray crystal structures of two different iron(III) porphyrinates: [Fe(OEP)(NO3)] and [Fe(TPP)(NO3)]. The first complex has the nitrate ion coordinated by a single oxygen atom while the second derivative has the nitrate coordinated in a symmetric bidentate fashion. This latter structure is a redetermination that shows some differences from an earlier structure; the difference appears to be the result of an unrecognized nitrate ion disorder in the earlier structure determination. Changes in physical properties of three species [Fe(TPivP)(NO3)], [Fe(OEP)(NO3)], and [Fe-(TPP)-(NO3)] as a function of coordination mode were examined by Mössbauer and EPR spectroscopies; EPR spectra appear to be most sensitive to the change in coordination mode.
Graphical abstractThe physical properties of high-spin nitrato-ligated iron(III) porphyrinates show differences depending on the mode of nitrate coordination.Figure optionsDownload full-size imageDownload as PowerPoint slide