Issue 21, 2017
From the journal:

Organic & Biomolecular Chemistry

Circularly polarised luminescence of pyrenyl di- and tri-peptides with mixed d- and l-amino acid residues†

Yuki Mimura,a   Tomoki Nishikawa,a   Ryo Fuchino,a   Shiho Nakai,a   Nobuo Tajima,b   Mizuki Kitamatsu,*a   Michiya Fujiki ORCID logo *c  and  Yoshitane Imai ORCID logo *a  

* Corresponding authors

a Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashi-Osaka, Osaka 577-8502, Japan
E-mail: y-imai@apch.kindai.ac.jp, kitamatu@apch.kindai.ac.jp

b Computational Materials Science Center, National Institute for Materials Science 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan

c Graduate School of Materials Science, Nara Institute of Science and Technology, Takayama, Ikoma, Nara 630-0192, Japan
E-mail: fujikim@ms.naist.jp

Abstract

Multiple pyrenes as pendants of enantioimpure di-/tripeptides (abbreviated as N-LD-C, N-DL-C, N-LLD-C and N-DDL-C) showed pyrene-origin CPL and CD signals, which were associated with conflicting CPL-/CD-signs, compared to the corresponding enantiopure di-/tri-peptides.

Graphical abstract: Circularly polarised luminescence of pyrenyl di- and tri-peptides with mixed d- and l-amino acid residues

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Article information

DOI
https://doi.org/10.1039/C7OB00503B
Article type
Paper
Submitted
28 Feb 2017
Accepted
07 Apr 2017
First published
07 Apr 2017

Org. Biomol. Chem., 2017,15, 4548-4553

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Circularly polarised luminescence of pyrenyl di- and tri-peptides with mixed D- and L-amino acid residues

Y. Mimura, T. Nishikawa, R. Fuchino, S. Nakai, N. Tajima, M. Kitamatsu, M. Fujiki and Y. Imai, Org. Biomol. Chem., 2017, 15, 4548 DOI: 10.1039/C7OB00503B

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