Reaction of Metal and Metalloid Compounds with Polyfunctional Molecules, XXVII) Reactions of N-Sulfinyl Compounds with ThioboranesThe reaction of N-sulfinylamines with (methy1thio)organylboranes proceeds quantitatively according to R -N = S = 0 + 3 R'zBSCH, + RN(BR',) -SSCH, + CH3SSCH3 + [(CH3),BI20 by insertion of the N = S double bond into the B-S sequence and a complex redox-reaction. The (dimethylboryl)(methyldithio)amines formed are monomeric; the course of the reaction depends on steric factors and reactive neighbouring groups. Thus compound 4 is obtained from 2-(sulfiny1amino)benzonitrile by twofold insertion and subsequent elimination of B(CH3),. The ring compounds 7, 8, and 9 are formed from N,N'-disulfinyldiamines and CH,B (SCH,), while the open-chain moieties 5 and 6 result from the reaction of difunctional N-sulfinylamines with (CH,),BSCH,. From N-sulfinylsulfonamides and dimethyl(methy1thio)borane N-(dimethylboryl)-N-(methy1dithio)sulfonamides (10) are obtained, and N-sulfinylbenzamide reacts with (CH3),BSCH3 to form the coordinatively dimerized compound 12. AU derivatives were characterized by analytical and spectroscopic (MS; NMR: 'H, "B, "F) methods. New N-sulfinylamines were synthesized as starting materials.
Die Umsetzung der N‐Sulfinylverbindungen (I) mit dem Thioboran (II) verläuft unter Einschiebung der N=S‐Bindung in die B‐S‐Bindung und einer komplexen Redoxreaktion zu den N‐Boryl‐N‐methyldithio‐aminen (III), die quantitativ erhalten werden; neben (IIIc) tritt als Nebenprodukt die Verbindung (IV) auf.
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