Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers
Transition-metal-catalyzed aryl-aryl coupling though C-H bonds activation, termed direct arylation, has been widely used in synthesis of a broad range of small molecules. In contrast to traditional coupling methods such as Suzuki coupling and Stille coupling, direct arylation does not involve tediou...
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sg-ntu-dr.10356-1062752019-12-06T22:07:51Z Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers Wang, Kai Wang, Mingfeng School of Chemical and Biomedical Engineering DRNTU::Science::Chemistry::Organic chemistry Transition-metal-catalyzed aryl-aryl coupling though C-H bonds activation, termed direct arylation, has been widely used in synthesis of a broad range of small molecules. In contrast to traditional coupling methods such as Suzuki coupling and Stille coupling, direct arylation does not involve tedious preparation of unstable, toxic organometallic reagents. Despite these advantages, direct arylation has not been applied to synthesis of π-conjugated polymers until recently. In this perspective, we summarize the progress of direct arylation polymerization for synthesis of various π-conjugated polymers, including homopolymers of polythiophene derivatives and donoracceptor alternating copolymers. We also discuss present challenges and future directions of this nascent methodology of polymerization for synthesis of functional π-conjugated polymers that can find applications in optoelectronic devices such as solar cells and field effect transistors. 2014-10-13T02:53:21Z 2019-12-06T22:07:50Z 2014-10-13T02:53:21Z 2019-12-06T22:07:50Z 2013 2013 Journal Article Wang, K., & Wang, M. (2013). Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers. Current organic chemistry, 17(9), 999-1012. 1385-2728 https://hdl.handle.net/10356/106275 http://hdl.handle.net/10220/24006 http://dx.doi.org/10.2174/1385272811317090011 en Current organic chemistry © 2013 Bentham Science Publishers. |
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DRNTU::Science::Chemistry::Organic chemistry Wang, Kai Wang, Mingfeng Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers |
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Transition-metal-catalyzed aryl-aryl coupling though C-H bonds activation, termed direct arylation, has been widely used in synthesis of a broad range of small molecules. In contrast to traditional coupling methods such as Suzuki coupling and Stille coupling, direct arylation does not involve tedious preparation of unstable, toxic organometallic reagents. Despite these advantages, direct arylation has not been applied to synthesis of π-conjugated polymers until recently. In this perspective, we summarize the progress of direct arylation polymerization for synthesis of various π-conjugated polymers, including homopolymers of polythiophene derivatives and donoracceptor alternating copolymers. We also discuss present challenges and future directions of this nascent methodology of polymerization for synthesis of functional π-conjugated polymers that can find applications in optoelectronic devices such as solar cells and field effect transistors. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Wang, Kai Wang, Mingfeng |
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Article |
author |
Wang, Kai Wang, Mingfeng |
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Wang, Kai |
title |
Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers |
title_short |
Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers |
title_full |
Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers |
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Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers |
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Direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers |
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direct arylation polymerization : a green, streamlining synthetic approach to π-conjugated polymers |
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2014 |
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https://hdl.handle.net/10356/106275 http://hdl.handle.net/10220/24006 http://dx.doi.org/10.2174/1385272811317090011 |
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