Stabilization of a Silaaldehyde by its η2 Coordination to Tungsten
Silylene
DOI:
10.1002/anie.201507956
Publication Date:
2015-11-24T12:32:40Z
AUTHORS (4)
ABSTRACT
Abstract Treatment of pyridine‐stabilized silylene complexes [(η 5 ‐C Me 4 R)(CO) 2 (H)WSiH(py)(Tsi)] (R=Me, Et; py=pyridine; Tsi=C(SiMe 3 ) with an N‐heterocyclic carbene I i Pr (1,3‐diisopropyl‐4,5‐dimethylimidazol‐2‐ylidene) caused deprotonation to afford anionic WSiH(Tsi)][H Pr] (R=Me ( 1‐Me ); R=Et 1‐Et )). Subsequent oxidation and pyridine‐ N ‐oxide (1 equiv) gave η ‐silaaldehydetungsten W{η ‐OSiH(Tsi)}][H 2‐Me 2‐Et The formation unprecedented W‐Si‐O three‐membered ring was confirmed by X‐ray crystal structure analysis.
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