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Title: C–H bond activation via concerted metalation–deprotonation at a palladium( iii ) center
Herein we report the direct observation of C–H bond activation at an isolated mononuclear Pd( iii ) center. The oxidation of the Pd( ii ) complex ( Me N4)Pd II (neophyl)Cl (neophyl = –CH 2 C(CH 3 ) 2 Ph; Me N4 = N , N ′-dimethyl-2,11-diaza[3.3](2,6)pyridinophane) using the mild oxidant ferrocenium hexafluorophosphate (FcPF 6 ) yields the stable Pd( iii ) complex [( Me N4)Pd III (neophyl)Cl]PF 6 . Upon the addition of an acetate source, [( Me N4)Pd III (neophyl)Cl]PF 6 undergoes Csp 2 –H bond activation to yield the cyclometalated product [( Me N4)Pd III (cycloneophyl)]PF 6 . This metalacycle can be independently prepared, allowing for a complete characterization of both the starting and final Pd( iii ) complexes. The C–H activation step can be monitored directly by EPR and UV-Vis spectroscopies, and kinetic isotope effect (KIE) studies suggest that either a pre-association step such as an agostic interaction may be rate limiting, or that the C–H activation is partially rate-limiting in conjunction with ligand rearrangement. Density functional theory calculations support that the reaction proceeds through a κ 3 ligand coordination and that the flexible ligand structure is important for this transformation. Overall, this study represents the first example of discrete C–H bond activation occurring at a Pd( iii ) center through a concerted metalation–deprotonation mechanism, akin to that observed for Pd( ii ) and Pd( iv ) centers.  more » « less
Award ID(s):
2102544
PAR ID:
10428402
Author(s) / Creator(s):
; ; ;
Date Published:
Journal Name:
Chemical Science
Volume:
14
Issue:
14
ISSN:
2041-6520
Page Range / eLocation ID:
3800 to 3808
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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