| Literature DB >> 27072533 |
René Labbow1, Dirk Michalik2, Fabian Reiß2, Axel Schulz3,4, Alexander Villinger1.
Abstract
A new synthetic approach enabled the generation of highly labile thionylimide, H-NSO, which was trapped by adduct formation with the bulky Lewis acid B(C6 F5 )3 and fully characterized. For comparison, a series of different Me3 Si-NSO Lewis acid adducts were studied. Treatment of Me3 Si-NSO with the silylium ion [Me3 Si](+) led to the formation of the hitherto unknown iminosulfonium ion [Me3 Si-N=S-O-SiMe3 ](+) , which could be isolated and fully characterized as a salt in the presence of weakly coordinating carborate anions.Entities:
Keywords: adducts; pseudohalogens; silylium cations; sulfinyl imines; thionyl imides
Year: 2016 PMID: 27072533 DOI: 10.1002/anie.201601878
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336