Orientational Control of Circularly Polarized Luminescence from Pyrene Clusters by Using a DNA Scaffold

Author:

Kashida Hiromu1ORCID,Ito Yuka1,Kakuta Takahiro2,Ogoshi Tomoki34,Asanuma Hiroyuki1

Affiliation:

1. Department of Biomolecular Engineering Graduate School of Engineering Nagoya University Furo-cho, Chikusa-ku Nagoya Aichi 464-8603 Japan

2. Graduate School of Natural Science and Technology Kanazawa University Kakuma-machi Kanazawa Ishikawa 920-1192 Japan

3. Department of Synthetic Chemistry and Biological Chemistry Graduate School of Engineering Kyoto University Katsura, Nishikyo-ku Kyoto 615-8510 Japan

4. WPI Nano Life Science Institute (WPI-NanoLSI) Kanazawa University Kakuma-machi Kanazawa Ishikawa 920-1192 Japan

Abstract

AbstractWe have investigated the chiroptical activities of pyrene clusters incorporated within a DNA duplex. Three pyrene derivatives were prepared on d‐threoninol linkers to allow incorporation within a DNA strand. DNA scaffolds containing dimers, tetramers, and hexamers of the pyrene derivatives were prepared. The homodimers of 1‐ and of 4‐pyrenecarboxylic acid, but not 2‐pyrenecarboxylic acid, emitted intense circularly polarized luminescence signals. Although increasing the number of pyrene units weakened the signal, insertion of natural base pairs between two dimers enhanced its intensity. Interestingly, circularly polarized luminescence intensities varied non‐monotonically depending on the number of intervening base pairs, thus indicating the importance of orientation between pyrene dimers. The results presented here could lead to the development of bright circularly polarized luminescence materials and probes.

Funder

Japan Society for the Promotion of Science

Precursory Research for Embryonic Science and Technology

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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