The
scission of a C(sp3)–H bond to form a new
metal–alkyl bond is a fundamental step in coordination chemistry
and catalysis. However, the extent of C–H bond weakening when
this moiety interacts with a transition metal is poorly understood
and quantifying this phenomenon could provide insights into designing
more efficient C–H functionalization catalysts. We present
a nickel complex with a robust adamantyl reporter ligand that enables
the measurement of C–H acidity (pKa) and bond dissociation free energy (BDFE) for a C(sp3)–H agostic interaction, showing a decrease in pKa by dozens of orders of magnitude and BDFE decrease of
about 30 kcal/mol upon coordination. X-ray crystallographic data is
provided for all molecules, including a distorted square planar NiIII metalloradical and “doubly agostic” NiII(κ2-CH2) complex