Probing the Dichotomy of Square Planar d¹⁰ Complexes: Geometric and Electronic Structure of Nickel π-Complexes

<div>Ni π-complexes are widely postulated as intermediates in organometallic chemistry. However, the nature of the bonding in such complexes has not been extensively studied. Herein, we probe the geometric and electronic structure of a series of nickel π-complexes using a combination of ³¹P NMR, Ni K-edge XAS, Ni K_β XES, and supporting density-functional computations. These complexes are best described as square planar d¹⁰ complexes with π-backbonding acting as the dominant factor in the M-L bond to the π ligand. The degree of backbonding correlates with both ²J_PP and the energy of the clearly observable Ni 1s→4p_z</div><div>pre-edge transition in the Ni K-edge XAS data. The degree of backbonding is determined by the energy of the π*_ip ligand acceptor orbital: unactivated olefinic ligands tend to be poor π-acids whereas ketones, aldehydes, and esters allow for greater backbonding. The strength of the backbonding from the neutral Ni(dtbpe) molecular fragment is dramatically increased via σ donation from the diphosphine ligands. In fact, in unactivated pi complexes, backbonding is dominated by charge donation from the phosphines, which allows for strong backdonation even though the metal centre retains a formal d¹⁰ electronic configuration. We describe this interaction as a formal 3-centre-4-electron (3c-4e) interaction where the nickel centre mediates charge transfer from the phosphine σ-donors to the π*_ip ligand acceptor orbital. The implications of this unusual bonding motif are described with respect to both geometric structure and reactivity.</div>

Density Functional Computations on 6-Aminouracil: Effect of Amino Group in the 6th Position on the Watson–Crick Base Pair Uridine–Adenosine

The predicted infrared and Raman spectra of 6-aminouracil in the solid state by density functional theory methods were analyzed and compared with the experimental spectra. The effect of amino substitution in the sixth position of uridine on the stability of the Watson–Crick (WC) base pairs with deoxyadenosine was evaluated. Different WC pairs of 5-aminouridine, 6-aminouridine, and uridine with deoxyadenosine were simulated, and the counterpoise-corrected interaction energies were determined. 6-Aminouridine produces a stronger WC pair than that involving uridine, and its high dipole moment facilitates interaction with water molecules.