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Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT
Novel [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) analogues containing benzo[b]thiophene (3a, 3b) and thieno[3,2-b]thiophene (3c, 3d) were synthesized and characterized. The morphology of the thin films prepared from the mixtures of these methanofullerenes with regioregular poly(3-hexylthiophe...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568877/ https://www.ncbi.nlm.nih.gov/pubmed/18941618 http://dx.doi.org/10.3762/bjoc.4.33 |
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author | Matsumoto, Fukashi Moriwaki, Kazuyuki Takao, Yuko Ohno, Toshinobu |
author_facet | Matsumoto, Fukashi Moriwaki, Kazuyuki Takao, Yuko Ohno, Toshinobu |
author_sort | Matsumoto, Fukashi |
collection | PubMed |
description | Novel [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) analogues containing benzo[b]thiophene (3a, 3b) and thieno[3,2-b]thiophene (3c, 3d) were synthesized and characterized. The morphology of the thin films prepared from the mixtures of these methanofullerenes with regioregular poly(3-hexylthiophene) (P3HT) was investigated by AFM measurement and UV-Vis absorption spectroscopy. A solubility test of these methanofullerenes was performed by using dichloromethane as a solvent. es-TThCBM (3d) exhibited 1.4 times greater solubility in dichloromethane than PCBM. |
format | Text |
id | pubmed-2568877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-25688772008-10-20 Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT Matsumoto, Fukashi Moriwaki, Kazuyuki Takao, Yuko Ohno, Toshinobu Beilstein J Org Chem Full Research Paper Novel [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) analogues containing benzo[b]thiophene (3a, 3b) and thieno[3,2-b]thiophene (3c, 3d) were synthesized and characterized. The morphology of the thin films prepared from the mixtures of these methanofullerenes with regioregular poly(3-hexylthiophene) (P3HT) was investigated by AFM measurement and UV-Vis absorption spectroscopy. A solubility test of these methanofullerenes was performed by using dichloromethane as a solvent. es-TThCBM (3d) exhibited 1.4 times greater solubility in dichloromethane than PCBM. Beilstein-Institut 2008-09-29 /pmc/articles/PMC2568877/ /pubmed/18941618 http://dx.doi.org/10.3762/bjoc.4.33 Text en Copyright © 2008, Matsumoto et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Matsumoto, Fukashi Moriwaki, Kazuyuki Takao, Yuko Ohno, Toshinobu Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT |
title | Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT |
title_full | Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT |
title_fullStr | Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT |
title_full_unstemmed | Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT |
title_short | Synthesis of thienyl analogues of PCBM and investigation of morphology of mixtures in P3HT |
title_sort | synthesis of thienyl analogues of pcbm and investigation of morphology of mixtures in p3ht |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568877/ https://www.ncbi.nlm.nih.gov/pubmed/18941618 http://dx.doi.org/10.3762/bjoc.4.33 |
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