Abstract
The innovative construction of novel N,O-bidentate ligands and N,O π-conjugated four-coordinate organoboron complexes represent a long-standing challenge for chemists. Here, we report an unprecedented and straightforward approach for the construction of N,O-bidentate ligands and their organoboron complexes via the merge of ring deconstruction with cycloaromatization of indolizines and cyclopropenones. Without any catalysts, our method is able to deliver a series of polyaryl 2-(pyridin-2-yl)phenol ligands, N,O π-conjugated organoboron (BF2 and BAr2) complexes with good functional-group compatibility which are difficult or even impossible to synthesize with previous methods. Importantly, the formed N,O-bidentate ligands were easy to scale up and derive with valuable drugs and active molecules. In addition, the photoluminescence measurements and the HOMO/LUMO gap have been investigated, the results have revealed that N,O π-conjugated tetracoordinate boron complexes display bright fluorescence, large Stokes shifts, and good quantum yields (Φlum = 0.15–0.45). The method proposed by the paper will inspire the development of various N,O-bidentate metal and boron complexes, which is expected to move the area of catalysis chemistry and material science forward.
Deconstructive Cycloaromatization Strategy towards N,O-Bidentate Ligands and Their Four-Coordinate Organoboron Complexes