Title of article :
Fluorothiazynes, 50 years old and still exciting: electrophilic attack at the thiazyl nitrogen of NSF2NS(O)F2
Author/Authors :
Mews، نويسنده , , Rüdiger and Borrmann، نويسنده , , Tobias and Hoppenheit، نويسنده , , Reinhard and Lork، نويسنده , , Enno and Parsons، نويسنده , , Simon and Petersen، نويسنده , , Jan and Schrِter، نويسنده , , Markus and Stohrer، نويسنده , , Wolf-Dieter and Waterfeld، نويسنده , , Alfred B. Watson Jr.، نويسنده , , Paul G.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
7
From page :
1649
To page :
1655
Abstract :
One of the most interesting compounds in sulfur nitrogen fluorine chemistry is NSF2NS(O)F2 (3) (reported by Glemser and Höfer 30 years ago): in the NS backbone a triple and a double bond are connected by a single bond. Electrophiles (metal cations, fluoro Lewis acids, “CH3+”) attack this multifunctional system exclusively at the thiazyl nitrogen of the triple bond. [M(NSF2NS(O)F2)4][AsF6]2 (M = Ni (4b), Cu (4c)), [Re(CO)5(NSF2NS(O)F2)][AsF6]− (5), F5A·NSF2NS(O)F2 (A = As (6), Sb (7)), F3B·NSF2NS(O)F2 (8) and [H3CNSF2NS(O)F2]+[AsF6]− (9) were isolated. The X-ray structures of 4c, 6, 8 and 9 are reported, bonding in these complexes is compared with the recently reported related NSAr2NS(X)Ar2 (X = O, NH) species.
Keywords :
Thiazyl compounds , Thiazynes , Sulfur nitrogen multiple bonds , Electrophilic attack , Fluoro Lewis acids , coordination compounds , X-ray structures , Alkylation
Journal title :
Journal of Fluorine Chemistry
Serial Year :
2004
Journal title :
Journal of Fluorine Chemistry
Record number :
1608548
Link To Document :
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