Solid state polymerization of poly(phthalocyaninatosiloxane)

K. G. Beltsios; T. J. Marks; S. H. Carr

doi:10.1016/0379-6779(89)90875-8

Solid state polymerization of poly(phthalocyaninatosiloxane)

K. G. Beltsios, T. J. Marks, S. H. Carr

Northwestern University

Research output: Contribution to journal › Article › peer-review

Abstract

A kinetic study of the solid state formation of poly(phthalocyaninatosiloxane) ([Si(Pc)O]_n), a candidate component of air-stable, light-weight, electrically conductive fibers, was performed. The initiation of reaction occurs at defect sites, whereas propagation takes place through a "chain polycondensation" scheme as a result of lattice (topochemical) control. An Avrami-type power 2 law fits the low temperature data up to high conversions and the high temperature data up to the reaction rate maximum. The maximum chain length is probably controlled by the relative phthalocyanine ring spacings of the reactant and product lattices.

Original language	English
Pages (from-to)	31-35
Number of pages	5
Journal	Synthetic Metals
Volume	29
Issue number	2-3
DOIs	https://doi.org/10.1016/0379-6779(89)90875-8
Publication status	Published - Mar 21 1989

ASJC Scopus subject areas

Electronic, Optical and Magnetic Materials
Condensed Matter Physics
Mechanics of Materials
Mechanical Engineering
Metals and Alloys
Materials Chemistry

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AU - Carr, S. H.

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AB - A kinetic study of the solid state formation of poly(phthalocyaninatosiloxane) ([Si(Pc)O]n), a candidate component of air-stable, light-weight, electrically conductive fibers, was performed. The initiation of reaction occurs at defect sites, whereas propagation takes place through a "chain polycondensation" scheme as a result of lattice (topochemical) control. An Avrami-type power 2 law fits the low temperature data up to high conversions and the high temperature data up to the reaction rate maximum. The maximum chain length is probably controlled by the relative phthalocyanine ring spacings of the reactant and product lattices.

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