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Linear polythioesters. XIV. Products of interfacial polycondensation isomeric di(mercaptomethyl) trimethylbenzenes with some aliphatic acid dichlorides

✍ Scribed by Wawrzyniec Podkościelny; Stanisława Szubińska


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
397 KB
Volume
35
Category
Article
ISSN
0021-8995

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✦ Synopsis


New polythioesters by interfacial polycondensation of 4,6-di(mercaptomethyl)-1,2,3,-trimethylbenzene, 3,5-di(mercaptomethyl)-1,2,4,-trimethylbenzene and 2,4-di(mercaptomethy1)-1,3,5-trimethylbenzene with adipoyl and sebacoyl chlorides were obtained. Process of polycondensation was carried out under the same condition as established earlier as an optimal for synthesis of polythioester from 2,5-di(mercaptomethy1)-1,4-dimethylbenzene and sebacoyl chloride. The conditions of polycondensation process were as follows: the organic phase benzenefiexane (l:l), ratio of aqueous to organic phase 1:1, the presence of 100% excess of NaOH as hydrogen chloride acceptor, temperature of reaction 15"C, little excess of acid dichloride with addition time 8.5 min.

The structure of all polythioesters was determined by elementary analysis, infrared spectra, and X-ray analysis. Initial decomposition and initial intensive decomposition temperature were defined by the curves of thermogravimetric analysis. The molecular weights for these polymers were determined by gel chromatography.


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✍ Wawrzyniec Podkoscjelny; Anna Kultys 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 313 KB

## Abstract New polythioesters of better physicochemical and mechanical properties have been obtained by interfacial polycondensation of 4,4′‐di(mercaptomethyl)benzophenone with terephthaloyl, isophthaloyl, and phthaloyl chlorides with the use of sodium hydroxide excess as a hydrogen chloride accep