Synthesis and molecular properties of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles for organic electronics obtained by a consecutive twofold Suzuki and twofold Cadogan reaction-Reference-Cited by-同舟云学术

Synthesis and molecular properties of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles for organic electronics obtained by a consecutive twofold Suzuki and twofold Cadogan reaction

Published:2016 Issue:26 Volume:4 Page:6270-6279
ISSN:2050-7526
Container-title:Journal of Materials Chemistry C
language:en
Short-container-title:J. Mater. Chem. C

Author:

Srour Hassan¹²³⁴⁵,Doan Thu-Hong¹²³⁴⁵,Silva Elisabeth Da¹²³⁴⁵,Whitby Richard J.⁶⁷,Witulski Bernhard¹²³⁴⁵

Affiliation:

1. Laboratoire de Chimie Moléculaire et Thio-organique

2. CNRS UMR 6507

3. Normandie Univ, ENSICAEN & UNICAEN

4. 14050 Caen

5. France

6. Chemistry, University of Southampton

7. UK

Abstract

A set of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles has been synthesized by twofold Suzuki–Miyaura, Cadogan andN-alkylation reactions starting fromN-hexyl-2,7-dibromo-3,6-dinitro carbazole.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/TC/C6TC02009G

Reference101 articles.

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