Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/3032
Title: Synthesis of aza-analogues of poly(isothianaphthene)
Authors: Huskic, M
VANDERZANDE, Dirk 
GELAN, Jan 
Issue Date: 1999
Publisher: ELSEVIER SCIENCE SA
Source: SYNTHETIC METALS, 99(2). p. 143-147
Abstract: The reaction of phthalic anhydride with phosphorus pentasulfide which gives poly(isothianaphthene) (PITN) has been extended to some other anhydrides and its derivatives (phthalimides and phthalhydrazide). The reaction with anhydrides leads to polymers, while the reaction with other derivatives can lead to thio, dithio compounds or polymers. Contrary to theoretical predictions, aza-analogues of PITN do not seem to have better electrical properties. The most conductive is polyisoindol with conductivity of 10(-4) S/cm, which is still 100 times lower than PITN synthesized under similar conditions. (C) 1999 Elsevier Science S.A. All rights reserved.
Notes: Natl Inst Chem, Ljubljana 1000, Slovenia. Univ Limburg, Div Chem, Inst Mat Res, B-3590 Diepenbeek, Belgium.Huskic, M, Natl Inst Chem, Ljubljana 1000, Slovenia.
Keywords: poly(thieno[3,4-b]pyridine); poly(thieno[3,4-c]pyridine); poly(thieno[3,4-b]pyrazine); polyisoindol; P4S10
Document URI: http://hdl.handle.net/1942/3032
DOI: 10.1016/S0379-6779(98)01477-5
ISI #: 000078934300009
Type: Journal Contribution
Validations: ecoom 2000
Appears in Collections:Research publications

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