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Solution NMR and X-Ray Structural Studies on Phthalocyaninatoiron Complexes

✍ Scribed by Ignacio Fernández; Paul S. Pregosin; Alberto Albinati; Silvia Rizzato; Ursula E. Spichiger-Keller; Tomas Nezel; Jorge F. Fernández-Sánchez


Publisher
John Wiley and Sons
Year
2006
Tongue
German
Weight
227 KB
Volume
89
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The addition of primary amines as solubilizing reagents for phthalocyaninatoiron complexes is shown to afford six‐coordinate bis(amine)phthalocyaninato complexes, i.e., [Fe(amine)~2~(pc)] 2 (amine = decan‐1‐amine) and 3 (amine = benzylamine), with the two new N‐donors occupying the trans‐axial positions. The new complexes were characterized by extensive NMR measurements in THF solution. For complex 3 with the benzylamine ligand, the solid‐state structure was determined by X‐ray diffraction methods. Complex 2 is sufficiently labile in THF solution to exchange one amine ligand against CO (gas) affording an equilibrium mixture containing [Fe(amine)(CO)(pc)] 4.


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