1999
DOI: 10.1088/0954-0083/11/2/003
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Polyimides Containing 1, 4-Dithiine Units and their Corresponding Thiophene 2, 3, 4, 5 Tetracarboxylimide Units

Abstract: Polyimides containing 1,4-dithiine units and corresponding thiophene units were synthesized by the nucleophilic substitution reaction of bis(dichloro-maleimide) arylene derivatives with sodium sulfide. Their structures were confirmed by IR and UV spectroscopy and elemental analysis. The polymers were characterized by viscosimetric measurements, softening points and thermogravimetric data.

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Cited by 8 publications
(9 citation statements)
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“…These polyamides have initial decomposition temperatures in the range 335-348 8C, and the temperature of 10% weight loss ranged between 392 and 415 8C, comparable with polyimides containing 1,4-dithiin units. [9] The DSC curves (first heating cycle at a heating rate of 10 8C/min) showed a similar thermal behaviour for all the studied polymers. No glass transition temperature (T g ) or melting endotherms were detected up to about 300 8C.…”
Section: Thermal Properties Of Polyamidesmentioning
confidence: 58%
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“…These polyamides have initial decomposition temperatures in the range 335-348 8C, and the temperature of 10% weight loss ranged between 392 and 415 8C, comparable with polyimides containing 1,4-dithiin units. [9] The DSC curves (first heating cycle at a heating rate of 10 8C/min) showed a similar thermal behaviour for all the studied polymers. No glass transition temperature (T g ) or melting endotherms were detected up to about 300 8C.…”
Section: Thermal Properties Of Polyamidesmentioning
confidence: 58%
“…N-(4-carboxyphenyl)-3,4-dichloromaleimide (1) was prepared by hydrolising N-(4-chloroformylphenyl)-3,4-dichloromaleimide. This monomer was prepared as described in the literature, [9] and recrystallised from acetonitrile, m.p. 315-319 8C (315-319 8C, [9] and A305 8C [10] ).…”
Section: Reagentsmentioning
confidence: 99%
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“…Tetrachlorobismaleimides (5a-c) were prepared by the reaction of 4,4 -bismaleimides with thionyl chloride in the presence of pyridine, according to the method described in our previous paper [33].…”
Section: Tetrachloro-and Tetraiodobismaleimides (5a-c and 6a-c)mentioning
confidence: 99%