Tripodal Podand Ligand with a Superhalogen Nature as an Effective Molecular Trap.

Tris(2-methoxyethyl) fluoroborate anion (TMEFA), anovel tripodal ligand based on the BF4- superhalogen anion, is proposed and was investigated theoretically using ab initio MP2 (second-order Moller-Plesset perturbational method) and OVGF (outer valence Green function) methods. The studied molecule comprises three 2-methoxyethoxy groups (-O-CH2-CH2-O-CH3) connected to a central boron atom, which results in the C-3-symmetry of the compound. The resulting anion was stable against fragmentation processes and its vertical electron detachment energy was found to be 5.72 eV. Due to its equilibrium structure resembling that of classical tripodal podands, the [F-B(O-CH2-CH2-O-CH3)(3)](-) anion is capable of binding metal cations using its three arms, and thus may form strongly bound ionic complexes such as [F-B(O-CH2-CH2-O-CH3)(3)](-)/Li+ and [F-B(O-CH2-CH2-O-CH3)(3)](-)/Mg2+. The binding energies predicted for such compounds far exceed those of the similar neutral classical podand ligands, which likely makes the [F-B(O-CH2-CH2-O-CH3)(3)](-) system a more effective molecular trap or steric shielding agent with respect to selected metal cations.