Beilstein Journal of Organic Chemistry (Jun 2012)

meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties

  • Raphael Reuter,
  • Hermann A. Wegner

DOI
https://doi.org/10.3762/bjoc.8.99
Journal volume & issue
Vol. 8, no. 1
pp. 877 – 883

Abstract

Read online

The investigation of multi-photochromic compounds constitutes a great challenge, not only from a synthetic point of view, but also with respect to the analysis of the photochemical properties. In this context we designed a novel strategy to access meta-oligoazobiphenyls via site-selective Mills reaction and Suzuki cross-coupling in a highly efficient iterative way. Photochemical examination of the resulting monomeric and oligomeric azo compounds revealed that the overall degree of switching was independent of the connected azo-units. However, one of the azobonds in the bis-azobiphenyl is isomerized preferentially despite the high structural similarity.

Keywords