Issue 80, 2017, Issue in Progress

Synthesis and photophysical studies of through-space conjugated [2.2]paracyclophane-based naphthalene fluorophores

Abstract

In this work we report a straightforward method for the synthesis of a new class of small organic fluorophores bearing both [2.2]paracyclophane and naphthalene subunits using an intramolecular dehydrogenative Diels–Alder reaction as a key step. These compounds are characterized by a compact three-dimensional structure as well as through-space conjugated push–pull systems, and possess interesting spectroscopic characteristics that may be useful for the development of innovative chemical probes and optical sensors.

Graphical abstract: Synthesis and photophysical studies of through-space conjugated [2.2]paracyclophane-based naphthalene fluorophores

Supplementary files

Article information

Article type
Paper
Submitted
08 Sep 2017
Accepted
23 Oct 2017
First published
30 Oct 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 50472-50476

Synthesis and photophysical studies of through-space conjugated [2.2]paracyclophane-based naphthalene fluorophores

E. Benedetti, M.-L. Delcourt, B. Gatin-Fraudet, S. Turcaud and L. Micouin, RSC Adv., 2017, 7, 50472 DOI: 10.1039/C7RA10038H

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