## Abstract 8‐Bromoadenine was benzylated in the presence of base to give a mixture of two regioisomers. One was easily recognized as 9‐benzyl‐8‐bromoadenine, but the other structure could not be determined with absolute certainty by NMR. Therefore, X‐ray crystallography was used to prove that the
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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