| Literature DB >> 31226235 |
Yaping Zang1, Ilana Stone2, Michael S Inkpen1, Fay Ng2, Tristan H Lambert3, Colin Nuckolls2, Michael L Steigerwald2, Xavier Roy2, Latha Venkataraman1,2.
Abstract
A single-molecule method has been developed based on the scanning tunneling microscope (STM) to selectively couple a series of aniline derivatives and create azobenzenes. The Au-catalyzed oxidative coupling is driven by the local electrochemical potential at the nanostructured Au STM tip. The products are detected in situ by measuring the conductance and molecular junction elongation and compared with analogous measurements of the expected azobenzene derivatives prepared ex situ. This single-molecule approach is robust, and it can quickly and reproducibly create reactions for a variety of anilines. We further demonstrate the selective synthesis of geometric isomers and the assembly of complex molecular architectures by sequential coupling of complementary anilines, demonstrating unprecedented control over bond formation at the nanoscale.Entities:
Keywords: aniline; azobenzene; electrocatalysis; electrooxidation; single-molecule measurements
Year: 2019 PMID: 31226235 DOI: 10.1002/anie.201906215
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336