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Inter- and intramolecular excimer circularly polarised luminescence of planar chiral paracyclophane-pyrene luminophores.
Hara, Nobuyuki; Shizuma, Motohiro; Harada, Takunori; Imai, Yoshitane.
Afiliação
  • Hara N; Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University 3-4-1 Kowakae, Higashi-Osaka Osaka 577-8502 Japan y-imai@apch.kindai.ac.jp.
  • Shizuma M; Department of Biochemistry, Osaka Research Institute of Industrial Science and Technology 1-6-50 Morinomiya, Joto-ku Osaka 536-8553 Japan.
  • Harada T; Department of Integrated Science and Technology, Faculty of Science and Technology, Oita University Dannoharu, 700 Oita City 870-1192 Japan.
  • Imai Y; Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University 3-4-1 Kowakae, Higashi-Osaka Osaka 577-8502 Japan y-imai@apch.kindai.ac.jp.
RSC Adv ; 10(19): 11335-11338, 2020 Mar 16.
Article em En | MEDLINE | ID: mdl-35495310
ABSTRACT
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 CHCl3 solution. In contrast, (R)/(S)-2 with 2-pyrene units exhibited a blue intramolecular excimer CPL at 450 nm in CHCl3 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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article