Fluoride-mediated alkoxylation and alkylthio-functionalization of halogenated perylenediimides-Reference-Cited by-同舟云学术

Fluoride-mediated alkoxylation and alkylthio-functionalization of halogenated perylenediimides

Published:2017 Issue:10 Volume:4 Page:2016-2021
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zink-Lorre N.¹²³⁴⁵^ORCID,Font-Sanchis E.¹²³⁴⁵^ORCID,Sastre-Santos Á.¹²³⁴⁵^ORCID,Fernández-Lázaro F.¹²³⁴⁵^ORCID

Affiliation:

1. Área de Química Orgánica

2. Instituto de Bioingeniería

3. Universidad Miguel Hernández de Elche

4. 03202 Elche

5. Spain

Abstract

The presence of fluoride ions in the reaction of chloro- or bromo-PDIs with alcohols and thiols leads to a spectacular increase in the yields of substituted compounds.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C7QO00337D

Reference42 articles.

1. Cyclic Carboxylic Imide Structures as Structure Elements of High Stability. Novel Developments in Perylene Dye Chemistry

2. Perylene bisimide dyes as versatile building blocks for functional supramolecular architectures

3. Control of the Interactions in Multichromophores: Novel Concepts. Perylene Bis-imides as Components for Larger Functional Units

4. Bay-substituted perylene bisimides: Twisted fluorophores for supramolecular chemistry

5. From Industrial Colorants to Single Photon Sources and Biolabels: The Fascination and Function of Rylene Dyes

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