Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells
Synthesis of poly(2-hexylthieno[3,4-b]thiophene-co-4,8-didodecyloxybenzo[1, 2-b:4, 5-b-]dithiophene) (PTB) is presented using a simple and low cost method. Anhydrous DMF and toluene was added into the mixture of 4,6-dibromo-2- hexylthieno[3,4-b] thiophene,2,6-Bis(trimethyltin)-4,8-didodecyloxybenzo[...
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th-cmuir.6653943832-523752018-09-04T09:36:27Z Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells C. Khantha T. Yakhanthip C. M. Macneill P. Pornprasit V. Kruefu N. Kungwan R. C. Coffin S. Phanichphant D. L. Carroll Chemistry Materials Science Physics and Astronomy Synthesis of poly(2-hexylthieno[3,4-b]thiophene-co-4,8-didodecyloxybenzo[1, 2-b:4, 5-b-]dithiophene) (PTB) is presented using a simple and low cost method. Anhydrous DMF and toluene was added into the mixture of 4,6-dibromo-2- hexylthieno[3,4-b] thiophene,2,6-Bis(trimethyltin)-4,8-didodecyloxybenzo[1,2-b: 4,5-b-]dithiophene and Pd(PPh3)4. The polymerization was carried out at 120?C for 12 h. The PTB product was precipitated in methanol and dried in vacuum. The HOMO and LUMO energies of the polymer were calculated using Density Functional Theory (DFT) calculations to be compared with the experimental results. Copyright © Taylor & Francis Group, LLC. 2018-09-04T09:24:16Z 2018-09-04T09:24:16Z 2013-09-27 Journal 15635287 15421406 2-s2.0-84884522408 10.1080/15421406.2013.803430 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84884522408&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/52375 |
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Chemistry Materials Science Physics and Astronomy C. Khantha T. Yakhanthip C. M. Macneill P. Pornprasit V. Kruefu N. Kungwan R. C. Coffin S. Phanichphant D. L. Carroll Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells |
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Synthesis of poly(2-hexylthieno[3,4-b]thiophene-co-4,8-didodecyloxybenzo[1, 2-b:4, 5-b-]dithiophene) (PTB) is presented using a simple and low cost method. Anhydrous DMF and toluene was added into the mixture of 4,6-dibromo-2- hexylthieno[3,4-b] thiophene,2,6-Bis(trimethyltin)-4,8-didodecyloxybenzo[1,2-b: 4,5-b-]dithiophene and Pd(PPh3)4. The polymerization was carried out at 120?C for 12 h. The PTB product was precipitated in methanol and dried in vacuum. The HOMO and LUMO energies of the polymer were calculated using Density Functional Theory (DFT) calculations to be compared with the experimental results. Copyright © Taylor & Francis Group, LLC. |
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C. Khantha T. Yakhanthip C. M. Macneill P. Pornprasit V. Kruefu N. Kungwan R. C. Coffin S. Phanichphant D. L. Carroll |
author_facet |
C. Khantha T. Yakhanthip C. M. Macneill P. Pornprasit V. Kruefu N. Kungwan R. C. Coffin S. Phanichphant D. L. Carroll |
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C. Khantha |
title |
Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells |
title_short |
Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells |
title_full |
Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells |
title_fullStr |
Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells |
title_full_unstemmed |
Synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells |
title_sort |
synthesis of copolymer thieno[3,4-b]thiophene and benzodithiophene for application in solar cells |
publishDate |
2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84884522408&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/52375 |
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