Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applications-Reference-Cited by-同舟云学术

Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applications

Published:2018 Issue:4 Volume:6 Page:761-766
ISSN:2050-7526
Container-title:Journal of Materials Chemistry C
language:en
Short-container-title:J. Mater. Chem. C

Author:

Josse Pierre¹²³⁴⁵,Li Shi⁶⁷⁸⁹,Dayneko Sergey¹⁰¹¹¹²¹³^ORCID,Joly Damien¹⁴¹⁵¹⁶¹⁷¹⁸,Labrunie Antoine¹²³⁴⁵,Dabos-Seignon Sylvie¹²³⁴⁵,Allain Magali¹²³⁴⁵,Siegler Benjamin¹⁹³⁴⁵²⁰,Demadrille Renaud¹⁴¹⁵¹⁶¹⁷¹⁸^ORCID,Welch Gregory C.¹⁰¹¹¹²¹³^ORCID,Risko Chad⁶⁷⁸⁹^ORCID,Blanchard Philippe¹²³⁴⁵,Cabanetos Clément¹²³⁴⁵^ORCID

Affiliation:

1. CNRS UMR 6200

2. MOLTECH-Anjou

3. University of Angers

4. 2 Bd Lavoisier

5. 49045 Angers

6. Department of Chemistry & Center for Applied Energy Research

7. University of Kentucky

8. Lexington

9. USA

10. Department of Chemistry, University of Calgary

11. 2500 University Drive N.W.

12. Calgary

13. Canada

14. University Grenoble Alpes

15. CNRS

16. CEA, INAC-SyMMES

17. UMR 5819

18. Grenoble

19. PIAM

20. France

Abstract

The synthesis for monobrominated benzothioxanthene is reported, which is then employed in common palladium catalyzed coupling reactions for novel organic semiconductors.

Funder

Office of Naval Research

Natural Sciences and Engineering Research Council of Canada

Canada Foundation for Innovation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/TC/C7TC05245F

Reference36 articles.

1. Synthetic Principles for Bandgap Control in Linear π-Conjugated Systems