Add time:07/25/2019         Source:sciencedirect.com

We report in this communication the easy preparation of the α-iodo substituted tripods within the series of tris(2-pyridylmethyl)amine (cas 16858-01-8) ligands, I1TPA, I2TPA and I3TPA, respectively. The characterization of the corresponding FeCl2 complexes in solution is described and structural analysis by X-ray diffraction for I1TPAFeCl2 and I2TPAFeCl2 is also reported. The steric effect of the iodo substituent is evidenced: (i) by elongation of the metal to iodo-pyridine distance within I1TPAFeCl2, which however remains a very stable compound; (ii) by decoordination of one substituted pyridine in I2TPAFeCl2 and I3TPAFeCl3. In I2TPAFeCl2 and in the solid state, this uncoordinated pyridine strongly interacts with the same fragment of the neighbouring molecule, providing an overall dinuclear arrangement for this complex.

► The α-iodo substituted tripods I1TPA, I2TPA and I3TPA have been prepared. ► The crystal structures of the high-spin complexes I1TPAFeCl2 and I2TPAFeCl2 are reported. ► I1TPAFeCl2 exhibits the expected distorted octahedral geometry. ► Intramolecular π-stacking of two adjacent molecules occurs in solid state in I2TPAFeCl2.

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