3.8 Article Proceedings Paper

Nonstoichiometric polycondensation I.: Synthesis of polythioether from dibromomethane and 4,4′-thiobisbenzenethiol

Journal

MACROMOLECULAR SYMPOSIA
Volume 199, Issue -, Pages 23-35

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/masy.200350903

Keywords

dibromomethane; kinetics; polycondensation; poly(phenylene thioether); stoichiometric imbalance

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High molecular weight poly(phenylene thioether) (3) was successfully obtained by the polycondensation of 4,4'-thiobisbenzenethiol (1) and dibromomethane (2) with a variety of feed ratios in the presence of 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU) in 1-methyl-2-pyrrolidinone (NMP) at 75 degreesC. The resulting polymer showed the maximum inherent viscosity (eta(inh)) of 0.50 dL/g in 4 h when 1.5 equivalents excess of 2 was used. The model reaction using benzenethiol (4) and dichloromethane (5) in the presence of DBU in deuterated dimethylsulfoxide (DMSO-d(6)) at 25 degreesC indicated that the rate of the second nucleophilic displacement reaction (k(2)) is 61 times faster than that of the first one (k(1)). The maximum of theoretical molecular weights calculated at various stoichiometric imbalance (S) under the condition of k(2)/k(1) = 61 showed a good agreement with the experimental molecular weights at specific polymerization times.

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