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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...

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Autores principales: Hara, Nobuyuki, Shizuma, Motohiro, Harada, Takunori, Imai, Yoshitane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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