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Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light

Superchiral light, generated by the interference of two counter-propagating circularly polarized light (CPL) with same frequency, opposite handedness and different intensity, exhibits enhanced dissymmetry in its interaction with chiral molecules, and has the potential for ultrasensitive detection an...

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Autores principales: He, Chenlu, Yang, Guang, Kuai, Yan, Shan, Sizhen, Yang, Lin, Hu, Jingang, Zhang, Douguo, Zhang, Qijin, Zou, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269450/
https://www.ncbi.nlm.nih.gov/pubmed/30504770
http://dx.doi.org/10.1038/s41467-018-07533-y
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author He, Chenlu
Yang, Guang
Kuai, Yan
Shan, Sizhen
Yang, Lin
Hu, Jingang
Zhang, Douguo
Zhang, Qijin
Zou, Gang
author_facet He, Chenlu
Yang, Guang
Kuai, Yan
Shan, Sizhen
Yang, Lin
Hu, Jingang
Zhang, Douguo
Zhang, Qijin
Zou, Gang
author_sort He, Chenlu
collection PubMed
description Superchiral light, generated by the interference of two counter-propagating circularly polarized light (CPL) with same frequency, opposite handedness and different intensity, exhibits enhanced dissymmetry in its interaction with chiral molecules, and has the potential for ultrasensitive detection and characterization of chiral molecules. It is anticipated that the enhanced optical dissymmetry in superchiral light (SCL) field may be utilized to promote asymmetric photochemical reactions efficiency. Herein we reported SCL impart greater chiral bias to trigger asymmetric photo-polymerization reaction from initially achiral diacetylene (DA) monomer, and the enhanced optical dissymmetry for whole polydiacetylene (PDA) films could be achieved. An explanation based on the chiral transfer and amplification of chiral bias from SCL during the polymerization process has been proposed. Moreover, thus formed chiral PDA films polymerized by SCL exhibited enhanced enantioselective recognition ability, and can serve as a direct visual probe for the discrimination of some specific enantiomers.
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spelling pubmed-62694502018-12-03 Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light He, Chenlu Yang, Guang Kuai, Yan Shan, Sizhen Yang, Lin Hu, Jingang Zhang, Douguo Zhang, Qijin Zou, Gang Nat Commun Article Superchiral light, generated by the interference of two counter-propagating circularly polarized light (CPL) with same frequency, opposite handedness and different intensity, exhibits enhanced dissymmetry in its interaction with chiral molecules, and has the potential for ultrasensitive detection and characterization of chiral molecules. It is anticipated that the enhanced optical dissymmetry in superchiral light (SCL) field may be utilized to promote asymmetric photochemical reactions efficiency. Herein we reported SCL impart greater chiral bias to trigger asymmetric photo-polymerization reaction from initially achiral diacetylene (DA) monomer, and the enhanced optical dissymmetry for whole polydiacetylene (PDA) films could be achieved. An explanation based on the chiral transfer and amplification of chiral bias from SCL during the polymerization process has been proposed. Moreover, thus formed chiral PDA films polymerized by SCL exhibited enhanced enantioselective recognition ability, and can serve as a direct visual probe for the discrimination of some specific enantiomers. Nature Publishing Group UK 2018-11-30 /pmc/articles/PMC6269450/ /pubmed/30504770 http://dx.doi.org/10.1038/s41467-018-07533-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
He, Chenlu
Yang, Guang
Kuai, Yan
Shan, Sizhen
Yang, Lin
Hu, Jingang
Zhang, Douguo
Zhang, Qijin
Zou, Gang
Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light
title Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light
title_full Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light
title_fullStr Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light
title_full_unstemmed Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light
title_short Dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light
title_sort dissymmetry enhancement in enantioselective synthesis of helical polydiacetylene by application of superchiral light
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269450/
https://www.ncbi.nlm.nih.gov/pubmed/30504770
http://dx.doi.org/10.1038/s41467-018-07533-y
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