A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues
In this research, pyreno[4,5‐c:9,10‐c′]difuran and its analogues have been successfully synthesized through a one‐step reaction using the same precursor and their physicochemical properties were studied. UV/Vis, fluorescence and CV measurements illustrated that the inserted chalcogen atoms (O, S and...
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sg-ntu-dr.10356-1398282020-05-29T06:23:09Z A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues Chen, Wangqiao Long, Guankui Kanehira, Koji Zhang, Mingtao Michinobu, Tsuyoshi Liu, Ming Zhang, Qichun School of Materials Science & Engineering School of Physical and Mathematical Sciences Research Techno Plaza Temasek Laboratories Engineering::Materials Isoarene Lawesson’s Reagent In this research, pyreno[4,5‐c:9,10‐c′]difuran and its analogues have been successfully synthesized through a one‐step reaction using the same precursor and their physicochemical properties were studied. UV/Vis, fluorescence and CV measurements illustrated that the inserted chalcogen atoms (O, S and Se) brought almost no change on the photochemical and electrochemical properties whereas TM‐2N‐CH3 exhibited more blue‐shifted fluorescence emission and simultaneously elevated HOMO energy level. MOE (Min. of Education, S’pore) 2020-05-22T02:56:19Z 2020-05-22T02:56:19Z 2018 Journal Article Chen, W., Long, G., Kanehira, K., Zhang, M., Michinobu, T., Liu, M., & Zhang, Q. (2018). A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues. Asian Journal of Organic Chemistry, 7(11), 2213-2217. doi:10.1002/ajoc.201800122 2193-5807 https://hdl.handle.net/10356/139828 10.1002/ajoc.201800122 2-s2.0-85046030339 11 7 2213 2217 en Asian Journal of Organic Chemistry © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved. |
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Engineering::Materials Isoarene Lawesson’s Reagent Chen, Wangqiao Long, Guankui Kanehira, Koji Zhang, Mingtao Michinobu, Tsuyoshi Liu, Ming Zhang, Qichun A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues |
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In this research, pyreno[4,5‐c:9,10‐c′]difuran and its analogues have been successfully synthesized through a one‐step reaction using the same precursor and their physicochemical properties were studied. UV/Vis, fluorescence and CV measurements illustrated that the inserted chalcogen atoms (O, S and Se) brought almost no change on the photochemical and electrochemical properties whereas TM‐2N‐CH3 exhibited more blue‐shifted fluorescence emission and simultaneously elevated HOMO energy level. |
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School of Materials Science & Engineering Chen, Wangqiao Long, Guankui Kanehira, Koji Zhang, Mingtao Michinobu, Tsuyoshi Liu, Ming Zhang, Qichun |
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Chen, Wangqiao Long, Guankui Kanehira, Koji Zhang, Mingtao Michinobu, Tsuyoshi Liu, Ming Zhang, Qichun |
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Chen, Wangqiao |
title |
A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues |
title_short |
A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues |
title_full |
A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues |
title_fullStr |
A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues |
title_full_unstemmed |
A direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues |
title_sort |
direct method to access substituted pyreno[4,5-c : 9,10-c’] difuran and its analogues |
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2020 |
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https://hdl.handle.net/10356/139828 |
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1681057433745620992 |