Homo- and hetero-dinuclear nickel(II), copper(II), and oxidovanadium(IV) complexes of a Schiff-base-fused phthalocyanine with 2,6-dimethylphenoxy and t-butyl groups

• Phthalocyanine fused with Schiff-base.
• M1(pc)–M2(salen) homo- and hetero-dinuclear complexes.
• Widely split Q bands over 600–800 nm.
• Ferro- and antiferromagnetic interactions within the dimers.

Homo- and hetero-dinuclear nickel(II), copper(II), and oxidovanadium(IV) complexes of a Schiff-base-fused phthalocyanine (pc) with bulky substituents, 2,6-dimethylphenoxy and t-butyl groups, were prepared and characterized. The introduced salen-like Schiff-base unit was shown to affect the spectral feature based on the pc unit in the near infrared region, the Q band being widely split over 600–800 nm. A fairly large ferromagnetic interaction (J = 6.0 cm−1) was observed for the CuII(pc)–CuII(salen) homo-dinuclear complex, while an antiferromagnetic interaction (J = −3.2 cm−1) was observed for the CuII(pc)–VIVO(salen) hetero-dinuclear complex.

Homo- and hetero-dinuclear nickel(II), copper(II), and oxidovanadium(IV) complexes of a Schiff-base-fused phthalocyanine ligand were synthesized and characterized. Widely split Q bands over 600–800 nm and intra-dimer magnetic interactions (J = 6.0 cm−1 for CuII(pc)–CuII(salen) and −3.2 cm−1 for the CuII(pc)–VIVO(salen)) were observed.Figure optionsDownload as PowerPoint slide