Method for preparing co-polymer luminescent material by electrochemical polymerization
A technology of luminescent materials and polymerization methods, which is applied in the field of preparation of copolymer luminescent materials, can solve the problems of cumbersome steps, high cost, and increased costs, and achieve the effects of wide range of monomers, easy industrial production, and low cost
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Embodiment 1
[0022] Electrochemical Copolymerization of 9,9'-Dihexylfluorene and Thiophene
[0023] Dissolve 9,9′-dihexylfluorene (0.01mol / L) and thiophene (0.1mol / L) in acetonitrile, and add tetrabutylammonium perchlorate 10 -2 mol / L, as an electrolyte. Add it to a three-electrode electrolytic cell, in which the working electrode is ITO glass; the counter electrode is platinum sheet; the reference electrode is silver-silver chloride electrode. Polymerization was carried out by a constant potential method, and the polymerization potential was 1.3V. Polymerization time 2h. After the polymerization is completed, the polymer on the ITO glass is scraped off, washed with absolute ethanol for 30 seconds, filtered, and vacuum-dried to obtain a copolymer powder.
Embodiment 2
[0025] Electrochemical Copolymerization of 9,9'-Dioctylfluorene and 3,4-Didecylthiophene
[0026] Dissolve 9,9′-dioctylfluorene (0.1mol / L) and 3,4-didecylthiophene (0.01mol / L) in acetonitrile, and add tetrabutylammonium perchlorate 10 -2 mol / L, as an electrolyte. Add it to a three-electrode electrolytic cell, in which the working electrode is ITO glass; the counter electrode is platinum sheet; the reference electrode is silver-silver chloride electrode. The polymerization was carried out by a constant potential method, and the polymerization potential was 1.1V. Polymerization time 1h seconds. After the polymerization is completed, the polymer on the ITO glass is scraped off, washed with absolute ethanol for 30 seconds, filtered, and vacuum-dried to obtain a copolymer powder.
Embodiment 3
[0028] Electrochemical Copolymerization of N-Butylcarbazole and 3-Butylthiophene
[0029] Dissolve N-butylcarbazole (0.1mol / L) and 3-butylthiophene (0.1mol / L) in boron trifluoride ether, join in the three-electrode electrolytic cell, wherein working electrode is ITO glass; The electrode is a platinum sheet; the reference electrode is a silver-silver chloride electrode. The polymerization was carried out by a constant potential method, and the polymerization potential was 1.1V. Polymerization time 48h. After the polymerization is completed, the polymer in the electrolytic cell is precipitated with methanol, filtered, washed with methanol, and vacuum-dried to obtain a copolymer powder.
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