| Literature DB >> 31050842 |
Zhenpin Lu1, Roy Lavendomme1, Olaf Burghaus2, Jonathan R Nitschke1.
Abstract
A redox-switchable self-assembled ZnII 4 L6 cage was synthesized that contains naphthalenediimide (NDI) motifs. Its reduction lent these NDI panels persistent radical anion character. The redox activity of this cage allows it to act as a catalyst for the oxidative coupling of different tetraaryl borates to give biaryls. The catalytic activity of the cage was enhanced following its binding of C60 , which implies a mechanism that does not involve encapsulation of the substrate.Entities:
Keywords: C−C coupling; fullerenes; host-guest chemistry; radicals; supramolecular catalysis
Year: 2019 PMID: 31050842 DOI: 10.1002/anie.201903286
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336