Lösliche (Tetraethylphthalocyaninato)eisen(II)‐ und ‐cobalt(II)‐Verbindungen

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Abstract
Soluble (Tetraethylphthalocyaninato)iron(II) and ‐cobalt(II) CompoundsThe (tetraethylphthalocyaninato)iron and ‐cobalt compounds Et4PcFe (9), Et4PcCo (8), and Et4PcH2(7) have been synthesized starting from 3,4‐dibromoacetophenone (1) via the corresponding dinitrile 5 or isoindolenine6, respectively. Et4PcFe (9) reacts withtBuNC,p‐diisocyanobenzene (dib), and me4dib to form the bisaxially coordinated compound Et4PcFe(tBuNc)2(10) and the oligomers [Et4PcFe(dib)]n(11) and [Et4PcFe‐ (me4dib)]n(12). All of the synthesized compounds, except the oligomers with a chain length of more than 8 – 14 units, are soluble in organic solvents such as chloroform or toluene. The new compounds were characterized by1H‐,13C‐NMR,13C‐CP/NMR, UV/Vis, and IR spectra. In addition the redox properties of Et4PcCo (8) were studied by cyclic voltammetry and spectroelectrochemical methods. The Mößbauer spectra of the (phthalocyaninato)iron compounds9, 11, and12demonstrate the bridged structure of [Et4PcFe(L)]n(L = dib, me4dib) (11,12). The powder conductivity of [Et4PcFe(dib)]n(11) (σRT= 5·10‐6S/cm) is ca. 106times higher than that of Et4PcFe (9) (σRT= 9·10‐12S/cm). After doping with iodine the oligomers11and12show an increase in conductivity of 105and 104, respectively (σRT≈︁ 10‐2S/cm for [Et4PcFe(dib)I0.85]n).

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