| Literature DB >> 27665723 |
Mickel J Hansen1, Michael M Lerch1, Wiktor Szymanski2,3, Ben L Feringa4.
Abstract
A straightforward synthesis of azobenzenes with bathochromically-shifted absorption bands is presented. It employs an ortho-lithiation of aromatic substrates, followed by a coupling reaction with aryldiazonium salts. The products are obtained with good to excellent yields after simple purification. Moreover, with the presented methodology, a structurally diverse panel of different azobenzenes, including unsymmetric tetra-ortho-substituted ones, can be readily obtained, which paves the way for future development of red-light-addressable azobenzene derivatives for in vivo application.Entities:
Keywords: azobenzenes; diazonium salts; lithiation; photochromism; red shift
Year: 2016 PMID: 27665723 DOI: 10.1002/anie.201607529
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336