Abstract
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. © 2012 Reuter and Wegner; licensee Beilstein-Institut.
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Reuter, R., & Wegner, H. A. (2012). Meta-Oligoazobiphenyls - Synthesis via site-selective Mills reaction and photochemical properties. Beilstein Journal of Organic Chemistry, 8, 877–883. https://doi.org/10.3762/bjoc.8.99
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