Divergent Synthesis of Heteroatom-Centered 4,8,12-Triazatriangulenes

Angew Chem Int Ed Engl. 2017 Apr 24;56(18):5087-5090. doi: 10.1002/anie.201701246. Epub 2017 Mar 29.

Abstract

The increasing attention devoted to triangulenes and their heteroatom derivatives inspired us to explore a divergent synthesis of heteroatom-centered 4,8,12-triazatriangulenes, which involved the preparation of a nitrogen-containing macrocyclic precursor and subsequent central heteroatom introduction by electrophilic C-Li and C-H substitution. The boron-centered triangulene has a planar structure unlike the bowl-shaped phosphorus- and silicon-centered triangulenes. The described synthetic procedure can be used to fabricate a broad range of attractive functional materials, for example, for organic light-emitting diodes, based on heteroatom-centered triangulenes.

Keywords: X-ray diffraction; divergent synthesis; electrophilic substitution; heterocycles; triangulenes.

Publication types

  • Research Support, Non-U.S. Gov't