Heteroatom-functionalized porphyrazines and multimetallic comple

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

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540122, 540139, 540140, 540145, C07D47822, C09B 4700, C09B 6200

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active

056750013

ABSTRACT:
Porphyrazine compounds having moieties substituted at the eight peripheral .beta.-pyrrole positions are disclosed. The porphyrazine compounds have the general structural formula: ##STR1## wherein M is H.sub.2 or a metal capable of complexing with the pyrrole nitrogen atoms, and A, B, C and D are independently selected from the group consisting of a thio moiety, an amino moiety, an oxo moiety, a phospho moiety, a seleno moiety, a telluro moiety and a non-coordinating moiety, like a hydrocarbon moiety, with the proviso that not all of A, B, C and D are a thio moiety and that not all of A, B, C, and D are a hydrocarbon moiety. The porphyrazine compounds, depending on the identity of A, B, C and D, are capable of complexing one to four metal ions to the periphery of the porphyrazine to form a multimetallic porphyrazine. Multimetallic porphyrazine compounds can be linked by the peripherally-complexed metal ions to form a linear, i.e., ribbon, polymer or a two-dimension, i.e., sheet polymer. The porphyrazine compounds, and the multimetallic complexes and polymers derived therefrom, are useful in, or as, magnet materials, molecular metal conductors, pharmaceuticals, imaging agents, and dyes.

REFERENCES:
Mani et al "Serendipitous Desymmetrisation During Porphyrazine Synthesis: an X-Ray Crystallographic Study of 2, 3, 7, 8, 12, 13, 17, 18-Octakis (Dimethylamino)-2-Secoporphyrazme-2, 3-dione", Journal of the Chemical Society, No. 17, 1994, pp. 1943-1944.
Elvridge et al., "Conjugated Macrocylces, Part XXVII, The Formation of Tetrazaporphins from Imidines," Tribenzotetrazaporphin, J. Chem. Soc., pp. 3536-3544, 1955.
Kopranenkov et al., "Phthalocyanines and Related Compounds," Journal of Organic Chemistry of the USSR, 15:5, Part 2, pp. 962-967, May, 1979.
Schramm et al., "Octakis(alkylthio)tetraazaporphyrins," Inorg. Chem., 19, pp. 383-385, 1980.
Velazquez et al., "Metal-Encapsulated Porphyrazines: Synthesis, X-ray Crystal Structure, and Spectroscopy of a Tetrain-star-Ni(porphyrazine)S.sub.8 Complex," J. Am. Chem. Soc., 112:20, pp. 7408-7410, 1990.
Velazquez et al., "star-Phorphyrazines: Synthetic, Structural, and Spectral Investigation of Complexes of the Polynucleating Porphyrazineoctathiolato Ligand," J. Am. Chem. Soc., 114, pp. 7416-7424, 1992.
Velazquez et al., "Star Porphyrazines: Peripheral Chelation of Porphyrazineoctathiolate by Diphosphinonickel Ions," J. Am. Chem. Soc., 115, pp. 9997-10003, 1993.
Mani et al., "Synthesis and Characterisation of Porphyrazinoctamine Derivatives: X-Ray Crystallographic Studies of and ," J. Chem. Soc., Chem. Commun., pp. 2095-2096, 1994.
Baumann et al., "Solitaire Porphyrazines: X-ray Crystal Structure and Spectroscopy of adium(II)," J. Am. Chem. Soc., 116, pp. 2639-2640, 1994.

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