Synthesis, properties, and catalysis of p-block complexes supported by bis(arylimino)acenaphthene ligands

• Published in: Communications chemistry Vol. 3; no. 1; p. 113
• Main Authors: Wang, Jingyi, Soo, Han Sen, Garcia, Felipe
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 12.08.2020; Nature Publishing Group
• Subjects: 639/638/263/406/939; 639/638/549/978; 639/638/911; Catalysis; Chemical synthesis; Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Coordination compounds; Ligands; Review; Review Article; Robustness; Scaffolds; Transition metals
• ISSN: 2399-3669; 2399-3669
• DOI: 10.1038/s42004-020-00359-0

Bis(arylimino)acenaphthene (Ar-BIAN) ligands have been recognized as robust scaffolds for metal complexes since the 1990 s and most of their coordination chemistry was developed with transition metals. Notably, there have been relatively few reports on complexes comprising main group elements, especially those capitalizing on the redox non-innocence of Ar-BIAN ligands supporting p -block elements. Here we present an overview of synthetic approaches to Ar-BIAN ligands and their p-block complexes using conventional solution-based methodologies and environmentally-benign mechanochemical routes. This is followed by a discussion on their catalytic properties, including comparisons to transition metal counterparts, as well as key structural and electronic properties of p-block Ar-BIAN complexes. Bis(arylimino)acenaphthene ligands were recognized as robust scaffolds for metal complexes decades ago, but their redox non-innocence as well as their potential to mediate electro- or photo-catalysis remain subjects of active research. Here, the authors review the synthesis and properties of these poly-aromatic diimine ligands complexed to nominally redox-innocent p -block elements.