ISSN:
0449-296X
Schlagwort(e):
Physics
;
Polymer and Materials Science
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Chemie und Pharmazie
Notizen:
This paper deals with some new methods for synthesis of the polymeric semiconductors by conjugated reactions and also with electrophysical properties of the polymers. Elimination of hydrogen halides from α,β-dihalo derivatives by bases (calcium oxide or tertiary amines) yields polymers with conjugated bonds. The reaction proceeds at 200-300°C. under atmospheric or elevated pressures, acetylenes being the intermediates. α,β-Dihalo compounds with calcium carbide above 150°C. produce polyacetylenic copolymers by elimination of two moles of hydrogen halide, also by generating acetylene from calcium carbide. The identical reaction (elimination of water) was observed between carbonyl compounds and calcium carbide. Elimination of water from monoand bifunctional phenols in the presence of zinc chloride under pressure above 200°C. yields polyphenylenes and polyhydroxyphenylenes, dehydrobenzene (benzyne) and hydroxybenzyne being intermediates. The polyhydroxyphenylenes prepared have a degree of polymerization from 4-5 to several thousand and are of interest as intermediates for thermostable resins, inhibitors etc. Linear polycyanamide and polycyanic acid were first prepared by polycondensation of urea with ammonium bicarbonate in the presence of zinc chloride. Analogous polymers were obtained from the ring-opening polymerization of melamine and cyanuric acid. The polymers show good semiconductor and ion-exchange properties. Polycondensation of ketones with ammonium bicarbonate also gave conjugated polymers. Thus, organometallic polymers were prepared from acetyl- and diacetyl ferrocene. We have also studied electrophysical, magnetic, and catalytic properties of the conjugated polymers prepared by the new methods. The electrical conductivity of the best specimens ranged from 10-3 to 10-6 ohm-1 cm.-1; the number of electrons unpaired was 1018-1019 spins/g.
Zusätzliches Material:
1 Tab.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1002/pol.1967.150050605
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