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Phthalocyanine polymers metal coordination complexes

This chapter describes the synthesis and properties of a number of classes of polymers containing metal coordination complexes in their structures. These polymers are prepared by polymerization reactions of metal-containing monomers and through metal coordination reactions. Schiff base-containing polymers (5) were one of the earUest classes of coordination polymers examined. Polymers incorporating macro-cycUc porphyrins and phthalocyanines (7) in their backbones and sidechains are known to exhibit interesting optical and electrical properties. The best-studied classes of metal-containing polymers contain bipyridyl and other related units coordinated to metal ions (8). [Pg.172]

Scheme 6 represents coordinate polymers. A low-molecular-weight compound with multidentate groups on both ends of the molecule grows into a linear polymer with metal ions, and the polymer chain is composed of coordinate bonds. The parquetlike polymer complexes, poly(metal-phthalocyanine) and poly(metal-tetracyano-ethylene), are classified into Scheme 7. They are formed by inserting metal ions into planar-network polymers or by causing a low-molecular-weight ligand derivative to react with a metal salt and a condensation reagent. Scheme 6 represents coordinate polymers. A low-molecular-weight compound with multidentate groups on both ends of the molecule grows into a linear polymer with metal ions, and the polymer chain is composed of coordinate bonds. The parquetlike polymer complexes, poly(metal-phthalocyanine) and poly(metal-tetracyano-ethylene), are classified into Scheme 7. They are formed by inserting metal ions into planar-network polymers or by causing a low-molecular-weight ligand derivative to react with a metal salt and a condensation reagent.
Recently, Shirai and Hojo25) have reported the synthesis of the soluble coordinate polymers containing metal-phthalocyanines in the main chain according to Scheme 2 (Eq. 7). The polymers obtained by polycondensation of metal-phthalocyanines bearing peripheral carboxy groups attached to various aromatics, -QH4-, -CsHr-CHz-CgH, exhibit higher conductivities (10-11 10-6 Q cm-1) than the corresponding monomer complexes. [Pg.160]


See other pages where Phthalocyanine polymers metal coordination complexes is mentioned: [Pg.98]    [Pg.478]    [Pg.573]    [Pg.686]    [Pg.26]    [Pg.573]    [Pg.97]    [Pg.160]    [Pg.418]    [Pg.356]    [Pg.328]    [Pg.10]    [Pg.172]    [Pg.668]    [Pg.388]    [Pg.296]   
See also in sourсe #XX -- [ Pg.179 , Pg.180 ]




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Complex polymers

Coordinating polymers

Coordination metal complexes

Metal coordination polymers

Metal phthalocyanine

Metal phthalocyanine complex

Metal phthalocyanines

Metallization, complex polymers

Phthalocyanine complexe

Phthalocyanine complexes

Phthalocyanine polymer

Phthalocyanines complexes

Phthalocyanines metal complexes

Phthalocyanines metallation

Phthalocyanines, coordination

Polymer complexation

Polymer coordination

Polymer metal complex

Polymers coordinated

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