| Literature DB >> 34766416 |
Xi Chen1, Hao Wang1, Shaozhi Du1, Matthias Driess2, Zhenbo Mo1.
Abstract
Herein, we report the efficient degradation of N2 O with a well-defined bis(silylene)amido iron complex as catalyst. The deoxygenation of N2 O using the iron silanone complex 4 as a catalyst and pinacolborane (HBpin) as a sacrificial reagent proceeds smoothly at 50 °C to form N2 , H2 , and (pinB)2 O. Mechanistic studies suggest that the iron-silicon cooperativity is the key to this catalytic transformation, which involves N2 O activation, H atom transfer, H2 release and oxygenation of the boron sites. This approach has been further developed to enable catalytic reductions of nitro compounds, producing amino-boranes with good functional-group tolerance and excellent chemoselectivity.Entities:
Keywords: Cooperativity; Iron; Nitrous oxide; Silanone complex; Silylene ligand
Year: 2021 PMID: 34766416 DOI: 10.1002/anie.202114598
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336