Abstract
Chromium(VI)
dialkyls are remarkably acidic, yielding a new set of anionic chromium
alkylidenes upon deprotonation with KN(TMS)2. We describe the characterization of three
anionic chromium alkylidenes of the type [(ArN)2Cr(=CHR)(CH2R]-
(R = tBu, SiMe3,
Ph; Ar = 2,6-diisopropylphenyl). NEt4[(ArN)2Cr(=CHSiMe3)(CH2SiMe3)]
has been structurally characterized by X-ray diffraction. We have also studied the C-H activation of
cyclohexane effected by the transient neopentylidene (ArN)2Cr(=CHCMe3).
This reaction generated a tri-nuclear chromium(IV) complex, namely ‘[Cr(NAr)2]3’,
as well as the two organic products cyclohexene and neopentane. A probable
intermediate in this reaction could be trapped by PPh3 to form (ArN)2Cr(PPh3)2. The latter undergoes ligand substitution
reactions with ethylene and CO to produce p-acid complexes of
tetravalent chromium.
Supplementary materials
Title
SI
Description
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