Journalartikel

Autorenliste: Griwatz, JH; Kunz, A; Wegner, HA

Jahr der Veröffentlichung: 2022

Seiten: 781-787

Zeitschrift: Beilstein Journal of Organic Chemistry

Bandnummer: 18

ISSN: 1860-5397

Open Access Status: Gold

DOI Link: https://doi.org/10.3762/bjoc.18.78

Verlag: Beilstein-Institut

Abstract: 
Azobenzene, as one of the most prominent molecular switches, is featured in many applications ranging from photopharmacology to information or energy storage. In order to easily and reproducibly synthesize non-symmetric substituted azobenzenes in an efficient way, especially on a large scale, the commonly used Baeyer???Mills coupling reaction was adopted to a continuous flow setup. The versatility was demonstrated with a scope of 20 substances and the scalability of this method exemplified by the synthesis of >70 g of an azobenzene derivative applied in molecular solar thermal storage (MOST) systems.

Harvard-Zitierstil: Griwatz, J., Kunz, A. and Wegner, H. (2022) Continuous flow synthesis of azobenzenes via Baeyer-Mills reaction, Beilstein Journal of Organic Chemistry, 18, pp. 781-787. https://doi.org/10.3762/bjoc.18.78

APA-Zitierstil: Griwatz, J., Kunz, A., & Wegner, H. (2022). Continuous flow synthesis of azobenzenes via Baeyer-Mills reaction. Beilstein Journal of Organic Chemistry. 18, 781-787. https://doi.org/10.3762/bjoc.18.78