Production process of electrically conducting polymer
A technology of conductive polymers and compounds, applied in the field of new π-conjugated polymers, can solve the problems of low conductivity, low conductivity and low concentration of reaction solution of conductive polymers
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Embodiment 1
[0076] 4 ml of distilled water was supplied into the reaction vessel, and 0.44 g (2.1 mmol, corresponding to 0.35 mol / L) of sodium 2-naphthalenesulfonate (hereinafter abbreviated as 2NaNS) was added as a surfactant. Subsequently, 0.28 g (2.0 mmol, corresponding to 0.33 mol / L) of 2,3-dihydrothiophene[3,4-b][1,4]dioxin (hereinafter abbreviated as HTDO) was added as a polymerizable monomer, stir the mixture. To this solution, a solution obtained by adding 0.28 g (0.7 mmol, corresponding to 0.12 mol / L) of iron(III) sulfate as an oxidizing agent to 2 ml of water was added dropwise over 1 hour to start the reaction. The reaction was carried out with stirring at a temperature of 20° C. for 15 hours. The resulting black polymer was filtered and the filtrate was washed with distilled water until the pH was 7. Then, the solution was washed twice with acetone, and vacuum-dried at 40° C. for 10 hours. The mass of the obtained polymer was 0.17 g. Subsequently, use a pressure of 3t / cm ...
Embodiment 2
[0078] The reaction was carried out under the same conditions as in Example 1, except that the amount of the surfactant was 0.55 g (2.6 mmol, equivalent to 0.44 mol / L). The mass of the obtained polymer was 0.17 g, and the results of measuring the electrical conductivity are shown in Table 1.
Embodiment 3
[0080] The reaction was carried out under the same conditions as in Example 1, except that the amount of the oxidizing agent was 0.20 g (0.5 mmol, equivalent to 0.086 mol / L). The mass of the obtained polymer was 0.16 g, and the results of measuring the electrical conductivity are shown in Table 1.
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