Issue 90, 2018
From the journal:

Chemical Communications

Structural effects of ditopic azoprobe–cyclodextrin complexes on the selectivity of guest-induced supramolecular chirality†

Shoji Fujiwara, ORCID logo ab   Kentaro Nonaka,b   Mai Yamaguchi,b   Takeshi Hashimoto ORCID logo b  and  Takashi Hayashita ORCID logo *b  

* Corresponding authors

a Department of Current Legal Studies, Faculty of Law, Meiji Gakuin University, 1518 Kamikurata-cho, Totsuka-ku, Yokohama, Japan

b Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, 7-1 Kioi-cho, Chiyoda-ku, Tokyo 102-8554, Japan
E-mail: ta-hayas@sophia.ac.jp

Abstract

Benzo-15-crown-5 and dipicolylamine are contained as the binding sites in a ditopic azoprobe (15C5-Azo-n-dpa). However, the selectivities of guest-induced supramolecular chirality for cations and anions were dramatically altered by a slight change in the spacer length of (15C5-Azo-n-dpa)2–γ-CyD complexes in water.

Graphical abstract: Structural effects of ditopic azoprobe–cyclodextrin complexes on the selectivity of guest-induced supramolecular chirality

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C8CC02242A
Article type
Communication
Submitted
20 Mar 2018
Accepted
16 Jun 2018
First published
17 Oct 2018
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2018,54, 12690-12693

Permissions

Request permissions

Structural effects of ditopic azoprobe–cyclodextrin complexes on the selectivity of guest-induced supramolecular chirality

S. Fujiwara, K. Nonaka, M. Yamaguchi, T. Hashimoto and T. Hayashita, Chem. Commun., 2018, 54, 12690 DOI: 10.1039/C8CC02242A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements