Quadrupolar, emission-tunable π-expanded 1,4-dihydropyrrolo[3,2-b]pyrroles – synthesis and optical properties-Reference-Cited by-同舟云学术

Quadrupolar, emission-tunable π-expanded 1,4-dihydropyrrolo[3,2-b]pyrroles – synthesis and optical properties

Published:2014 Issue:18 Volume:12 Page:2874-2881
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Janiga Anita¹²³,Bednarska Dominika¹²³,Thorsted Bjarne⁴⁵⁶,Brewer Jonathan⁴⁵⁶,Gryko Daniel T.¹²³⁷⁸

Affiliation:

1. Institute of Organic Chemistry

2. Polish Academy of Sciences

3. Warsaw, Poland

4. Department of Biochemistry and Molecular Biology

5. University of Southern Denmark

6. Odense 200-701, Denmark

7. Warsaw University of Technology

8. Faculty of Chemistry

Abstract

A–D–A chromophores containing pyrrolo[3,2-b]pyrrole, as a central donor moiety, display blue, turquoise, yellow and orange fluorescence, depending on the strength of the electron-withdrawing substituent.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB00143E

Reference91 articles.

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3. Thiophen-derivate und 1.2-Trithione

4. Palladium-Catalyzed C–S Coupling: Access to Thioethers, Benzo[b]thiophenes, and Thieno[3,2-b]thiophenes

5. A New Route to Annulated Oligothiophenes

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