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Ferrocene phosphazenes

Third, metallocene units, such as ferrocene or ruthenocene, have been linked to phosphazene cyclic trimers or tetramers and these were polymerized and substituted to give polymers of the type mentioned previously (41). Polyphosphazenes with ferrocenyl groups can be doped with iodine to form weak semiconductors. Polymer chains that bear both ruthenocenyl and ferrocenyl side groups are prospective electrode mediator systems. [Pg.261]

The earliest and most well-developed route to polyphosphazenes involves the thermal ROP of cyclic phosphazenes bearing halogen substituents at phosphorus. Use of this method and subsequent halogen replacement with alkoxides has led to the synthesis of ferrocene- and ruthenocene-containing polyphosphazenes 31 and 32 with molecular weights (d/w) in excess of 2 x... [Pg.308]

Polyphosphazenes with simple alkyl and aryl substituents directly attached to the backbone by P-C linkages can be prepared by the condensation polymerization of N-silylphosphoranimine precursors. These simple polymers can then be converted to a variety of functionalized polyphosphazenes by derivatization reactions. In this paper, the synthesis and characterization of some derivatives of poly(methylphenyl-phosphazene), [Me(Ph)P=N]and the copolymer, [Me(Ph)P=N]j [Me2P=N)y, are discussed. These polymers include grafted copolymers, water soluble carboxylated polymers, and polymers with silyl, vinyl, alcohol, ester, ferrocene, phosphine, thiophene, and/or fluoroalkyl groups. [Pg.333]

Ferrocene Substituents. Some of the most interesting poly(phosphazenes) that have been prepared from the reactions of the polymer anion 2 with carbonyl compounds are those with ferrocene substituents. [Pg.249]


See other pages where Ferrocene phosphazenes is mentioned: [Pg.95]    [Pg.408]    [Pg.345]    [Pg.347]    [Pg.348]    [Pg.393]    [Pg.1014]    [Pg.333]    [Pg.454]    [Pg.15]    [Pg.55]    [Pg.246]    [Pg.250]    [Pg.398]   
See also in sourсe #XX -- [ Pg.92 , Pg.97 ]




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Phosphazene

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