| Literature DB >> 32366961 |
Polly L Arnold1,2, Tatsumi Ochiai3,4, Francis Y T Lam3,4, Rory P Kelly3, Megan L Seymour3, Laurent Maron5.
Abstract
Chemists have spent over a hundred years trying to make ambient temperature/pressure catalytic systems that can convert atmospheric dinitrogen into ammonia or directly into amines. A handful of successful d-block metal catalysts have been developed in recent years, but even binding of dinitrogen to an f-block metal cation is extremely rare. Here we report f-block complexes that can catalyse the reduction and functionalization of molecular dinitrogen, including the catalytic conversion of molecular dinitrogen to a secondary silylamine. Simple bridging ligands assemble two actinide metal cations into narrow dinuclear metallacycles that can trap the diatom while electrons from an externally bound group 1 metal, and protons or silanes, are added, enabling dinitrogen to be functionalized with modest but catalytic yields of six equivalents of secondary silylamine per molecule at ambient temperature and pressure.Entities:
Year: 2020 PMID: 32366961 DOI: 10.1038/s41557-020-0457-9
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427