Aluminum and lithium octa(pentoxy)phthalocyanine radicals

A lithium phthalocyanine radical and the analogous aluminum phthalocyanine radical were synthesized as part of an investigation of isostructural dopants. An improved synthesis of the free base of octa(pentoxy)phthalocyanine (H2Pc*) involves the reduction of 1,2-dicyano-4,5-dipentoxybenzene with hydroquinone. Deprotonation with lithium bis(trimethylsilyl)amide leads to the dilithium derivative Li2Pc* and subsequent oxidation with ferrocenium yields the radical LiPc*. Treatment of H2Pc* with Et2AlCl gives ClAlPc* and reduction with sodium amalgam yields AlPc*, the first reported aluminum phthalocyanine radical. In the solid state LiPc* and AlPc* are electrical conductors with pressed-pellet conductivities of 8 × 10−11 Ω−1 cm−1 and 5 × 10−7 Ω−1 cm−1, respectively.

Graphical abstractThe synthesis and characterization of the aluminum and lithium octa(pentoxy)phthalocyanine radicals, AlPc* and LiPc*, are described. In the solid state LiPc* and AlPc* are electrical conductors with pressed-pellet conductivities of 8 × 10−11 Ω−1 cm−1 and 5 × 10−7 Ω−1 cm−1, respectively.Figure optionsDownload full-size imageDownload as PowerPoint slide