One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials

The one-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole, followed by alkylation and Stille coupling to yield three different isomeric derivatives with markedly different optoelectronic properties, is reported. These derivatives show potential as new units in organic oligomers and polymers...

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Main Authors: Tam, Teck Lip Dexter, Tan, Hong Hup Ronnie, Ye, Wanting, Mhaisalkar, Subodh Gautam, Grimsdale, Andrew C.
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/97249
http://hdl.handle.net/10220/10578
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-972492021-01-13T05:31:06Z One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials Tam, Teck Lip Dexter Tan, Hong Hup Ronnie Ye, Wanting Mhaisalkar, Subodh Gautam Grimsdale, Andrew C. School of Materials Science and Engineering Energy Research Institute @ NTU (ERI@N) The one-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole, followed by alkylation and Stille coupling to yield three different isomeric derivatives with markedly different optoelectronic properties, is reported. These derivatives show potential as new units in organic oligomers and polymers for electronics applications. 2013-06-25T02:22:39Z 2019-12-06T19:40:35Z 2013-06-25T02:22:39Z 2019-12-06T19:40:35Z 2011 2011 Journal Article Tam, T. L. D., Tan, H. H. R., Ye, W., Mhaisalkar, S. G., & Grimsdale, A. C. (2012). One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials. Organic letters, 14(2), 532-535. 1523-7060 https://hdl.handle.net/10356/97249 http://hdl.handle.net/10220/10578 10.1021/ol2031558 en Organic letters © 2011 American Chemical Society.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
description The one-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole, followed by alkylation and Stille coupling to yield three different isomeric derivatives with markedly different optoelectronic properties, is reported. These derivatives show potential as new units in organic oligomers and polymers for electronics applications.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Tam, Teck Lip Dexter
Tan, Hong Hup Ronnie
Ye, Wanting
Mhaisalkar, Subodh Gautam
Grimsdale, Andrew C.
format Article
author Tam, Teck Lip Dexter
Tan, Hong Hup Ronnie
Ye, Wanting
Mhaisalkar, Subodh Gautam
Grimsdale, Andrew C.
spellingShingle Tam, Teck Lip Dexter
Tan, Hong Hup Ronnie
Ye, Wanting
Mhaisalkar, Subodh Gautam
Grimsdale, Andrew C.
One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials
author_sort Tam, Teck Lip Dexter
title One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials
title_short One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials
title_full One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials
title_fullStr One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials
title_full_unstemmed One-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials
title_sort one-pot synthesis of 4,8-dibromobenzo[1,2-d;4,5-d′]bistriazole and synthesis of its derivatives as new units for conjugated materials
publishDate 2013
url https://hdl.handle.net/10356/97249
http://hdl.handle.net/10220/10578
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