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Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores
Two types of planar chiral [2,2]paracyclophane-pyrene luminophores (1 and 2) with different binding positions of the fluorescent pyrene units were synthesised. (R)/(S)-1 with 1-pyrene units exhibited green intermolecular excimer circularly polarised luminescence (CPL) at 530 nm in the KBr-pellet, bu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050457/ https://www.ncbi.nlm.nih.gov/pubmed/35495310 http://dx.doi.org/10.1039/d0ra01552k |
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author | Hara, Nobuyuki Shizuma, Motohiro Harada, Takunori Imai, Yoshitane |
author_facet | Hara, Nobuyuki Shizuma, Motohiro Harada, Takunori Imai, Yoshitane |
author_sort | Hara, Nobuyuki |
collection | PubMed |
description | Two types of planar chiral [2,2]paracyclophane-pyrene luminophores (1 and 2) with different binding positions of the fluorescent pyrene units were synthesised. (R)/(S)-1 with 1-pyrene units exhibited green intermolecular excimer circularly polarised luminescence (CPL) at 530 nm in the KBr-pellet, but exhibited no CPL signal in dilute CHCl(3) solution. In contrast, (R)/(S)-2 with 2-pyrene units exhibited a blue intramolecular excimer CPL at 450 nm in CHCl(3) solution. This is the first example of using the binding position of pyrene and the external environment to tune the type (inter- or intramolecular) and chiroptical sign of excimer CPL. |
format | Online Article Text |
id | pubmed-9050457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90504572022-04-29 Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores Hara, Nobuyuki Shizuma, Motohiro Harada, Takunori Imai, Yoshitane RSC Adv Chemistry Two types of planar chiral [2,2]paracyclophane-pyrene luminophores (1 and 2) with different binding positions of the fluorescent pyrene units were synthesised. (R)/(S)-1 with 1-pyrene units exhibited green intermolecular excimer circularly polarised luminescence (CPL) at 530 nm in the KBr-pellet, but exhibited no CPL signal in dilute CHCl(3) solution. In contrast, (R)/(S)-2 with 2-pyrene units exhibited a blue intramolecular excimer CPL at 450 nm in CHCl(3) solution. This is the first example of using the binding position of pyrene and the external environment to tune the type (inter- or intramolecular) and chiroptical sign of excimer CPL. The Royal Society of Chemistry 2020-03-20 /pmc/articles/PMC9050457/ /pubmed/35495310 http://dx.doi.org/10.1039/d0ra01552k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Hara, Nobuyuki Shizuma, Motohiro Harada, Takunori Imai, Yoshitane Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores |
title | Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores |
title_full | Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores |
title_fullStr | Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores |
title_full_unstemmed | Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores |
title_short | Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores |
title_sort | inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050457/ https://www.ncbi.nlm.nih.gov/pubmed/35495310 http://dx.doi.org/10.1039/d0ra01552k |
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