Synthesis and characterization of new thieno[3,2-b]thiophene derivatives

Synthesis and characterization of new thieno[3,2-b]thiophene derivatives

Three derivatives of thieno[3,2-b]thiophene end-capped with phenyl units have been synthesized and characterized by MALDI TOF mass spectroscopy, elemental analysis, UV-vis absorption spectroscopy and thermogravimetric analysis (TGA). All compounds were prepared using Pd-catalyzed Stille or Suzuki co...

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Main Authors: Ahmed, Moawia O., Pisula, Wojciech, Mhaisalkar, Subodh Gautam
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/96304
http://hdl.handle.net/10220/10234
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-963042023-07-14T15:46:47Z Synthesis and characterization of new thieno[3,2-b]thiophene derivatives Ahmed, Moawia O. Pisula, Wojciech Mhaisalkar, Subodh Gautam School of Materials Science & Engineering Three derivatives of thieno[3,2-b]thiophene end-capped with phenyl units have been synthesized and characterized by MALDI TOF mass spectroscopy, elemental analysis, UV-vis absorption spectroscopy and thermogravimetric analysis (TGA). All compounds were prepared using Pd-catalyzed Stille or Suzuki coupling reactions. Optical measurements and thermal analysis revealed that these compounds are promising candidates for p-type organic semiconductor applications. Published version 2013-06-12T03:33:51Z 2019-12-06T19:28:32Z 2013-06-12T03:33:51Z 2019-12-06T19:28:32Z 2012 2012 Journal Article Ahmed, M. O., Pisula, W., & Mhaisalkar, S. G. (2012). Synthesis and Characterization of New Thieno[3,2-b]thiophene Derivatives. Molecules, 17(10), 12163-12171. 1420-3049 https://hdl.handle.net/10356/96304 http://hdl.handle.net/10220/10234 10.3390/molecules171012163 en Molecules © 2012 The Author(s). This paper was published in Molecules and is made available as an electronic reprint (preprint) with permission of The Author(s). The paper can be found at the following official DOI: [http://dx.doi.org/10.3390/molecules171012163].  One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
description Three derivatives of thieno[3,2-b]thiophene end-capped with phenyl units have been synthesized and characterized by MALDI TOF mass spectroscopy, elemental analysis, UV-vis absorption spectroscopy and thermogravimetric analysis (TGA). All compounds were prepared using Pd-catalyzed Stille or Suzuki coupling reactions. Optical measurements and thermal analysis revealed that these compounds are promising candidates for p-type organic semiconductor applications.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Ahmed, Moawia O.
Pisula, Wojciech
Mhaisalkar, Subodh Gautam
format Article
author Ahmed, Moawia O.
Pisula, Wojciech
Mhaisalkar, Subodh Gautam
spellingShingle Ahmed, Moawia O.
Pisula, Wojciech
Mhaisalkar, Subodh Gautam
Synthesis and characterization of new thieno[3,2-b]thiophene derivatives
author_sort Ahmed, Moawia O.
title Synthesis and characterization of new thieno[3,2-b]thiophene derivatives
title_short Synthesis and characterization of new thieno[3,2-b]thiophene derivatives
title_full Synthesis and characterization of new thieno[3,2-b]thiophene derivatives
title_fullStr Synthesis and characterization of new thieno[3,2-b]thiophene derivatives
title_full_unstemmed Synthesis and characterization of new thieno[3,2-b]thiophene derivatives
title_sort synthesis and characterization of new thieno[3,2-b]thiophene derivatives
publishDate 2013
url https://hdl.handle.net/10356/96304
http://hdl.handle.net/10220/10234
_version_ 1772828468204011520

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