To pin down the nature of the β-agostic bond in late transition metal complexes, Scherer (Augsburg) and coworkers synthesized [(DCpH)Ni(dtbpe)]+[BF4]– (DCp = dicyclopentadiene, dtbpe = tBu2PCH2CH2PtBu2), a rigid β-agostic complex. In a combined experimental and theoretical study the charge density and NMR shifts were scrutinized.
To get good agreement with experiment, NMR calculations necessitated explicit spin-orbit coupling with hybrid GGAs in ADF. Diamagnetic (σd), paramagnetic (σp) and spin-orbit (σSOC) contributions to the shielding tensor of early and late transition metal complexes revealed that the 1H NMR chemical shift of the agostic H is determined mostly by σp while the atomic charge and σd at H remain rather constant in a variety of model systems studied. The term ‘hydridic shift’ to explain upfield shifts is therefore misleading. The experimental charge density analysis, in perfect agreement with AIM calculations in ADF, helps in further classifying β-agostic interactions. For late transition metal complexes, significant electron density builds up in the M-H bond at the expense of the C-H bond. An MO analysis reveals that the late transition metal β-agostic bond is well described by the classic Dewar-Chatt-Duncanson model for metal-alkenes, augmented with a M←L σ-donation term.
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AIM, spin-orbit coupling NMR, bonding analysis
W. Scherer, V. Herz, A. Bruck, C. Hauf, F. Reiner, S. Altmannshofer, D. Leusser, and D. Stalke, The Nature of β-Agostic Bonding in Late-Transition-Metal Alkyl Complexes Angew. Chem. Int. Ed. 50, 285 (2011)Key conceptsADF bonding analysis inorganic chemistry NMR Relativistic DFT spectroscopy