Abstract
The tungsten hydride [WH(CO)3(η-C5H5)] reacts with iminooxosulphuranes, RNSO (R = C6H4Me-2, C6H4Me-4), to give the tungsten sulphinamides [W{S(O)NHR}(CO)3(η-C5H5]. Diiminosulphuranes bearing electron-withdrawing substituents, R′NSNSO2C6H4Me-4 (R′ = C6H5, SO2C6H4Me-4), insert into the metalhydrogen bond of [WH(CO)3(η-C5H5)] to give [W{S(NR)NHSO2C6H4-Me-4}(CO)3(η-C5H5)], whilst bis(p-tolylimino)sulphurane, S(NC6H4Me-4)2, gives the tungstacycle [W{S(NHC6H4Me-4)N(C6H4ME-4)C(0)}(CO)2(η-C5H5)]. A comprehensive mechanism is discussed.
| Original language | English |
|---|---|
| Pages (from-to) | 303-310 |
| Number of pages | 8 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 371 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 1 Aug 1989 |
| Externally published | Yes |
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