Issue 86, 2017, Issue in Progress

Thiocarbamoyl in synthesis of the absorbent bis-mono and dimethine cyanine dyes incorporating porphyrin, thiazoles, thiazolones, thiadiazoles, pyrazoles and pyrazolones

Abstract

In this study, we have introduced an outlook dealing with synthetic heteroarenium-substituted pyridines 1 that are suitable as starting materials for the synthesis of a potential new thiocarbamoyl derivative 3 that may be of value in preparative organic and biological chemistry. Herein, a new series of twelve bis-mono and dimethine cyanine dyes incorporating different heterocyclic compounds were designed by efficient and simple reaction of compound 3 with various organic reagents to overcome the obstacles of energetic reactions, because they took long times. Moreover, the electronic behaviors of these compounds were studied because of their significant activity in many medical and other fields. The photosensitizers were elucidated by spectral and analytical analyses.

Graphical abstract: Thiocarbamoyl in synthesis of the absorbent bis-mono and dimethine cyanine dyes incorporating porphyrin, thiazoles, thiazolones, thiadiazoles, pyrazoles and pyrazolones

Supplementary files

Article information

Article type
Paper
Submitted
12 Sep 2017
Accepted
12 Nov 2017
First published
29 Nov 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 54706-54716

Thiocarbamoyl in synthesis of the absorbent bis-mono and dimethine cyanine dyes incorporating porphyrin, thiazoles, thiazolones, thiadiazoles, pyrazoles and pyrazolones

R. E. El-Mekawy and A. A. Fadda, RSC Adv., 2017, 7, 54706 DOI: 10.1039/C7RA10165A

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