Roberto Scipioni

A first principles investigation of water dipole moment in a defective continuous hydrogen bond network

First principles molecular dynamics simulations of an aqueous solution salt system at finite concentration containing both Na(+) and Cl(-) ions show that a change in the distribution of the molecular dipole moment of H(2)O monomers appears when ions are present in solution. Simulations suggest a lowering of the dipole moments of the water molecules in the solvation shells of Na(+) and Cl(-) as compared to the pure water case, while the dipoles of the rest of the molecules are hardly affected. However, finer analysis in terms of the Wannier centers distribution suggests a change in the electronic structure of the water molecules even in the bulk. Also a change of the H-bond network arrangement was found and correlation between dipole and MOH parameter evidences such subtle effects, suggesting a lowering of tetrahedral order in salty solutions. All these changes can be related to observable quantities such as the infrared spectra thus allowing for a rationalization of the experimental outcome on neutral aqueous solutions.

Water solvation properties: an experimental and theoretical investigation of salt solutions at finite dilution.

Our combined analysis of first-principle simulations and experiments conducted on salt solutions at finite dilution shows that the high frequency range of the infrared spectrum of an aqueous solution of NaCl displays a shift toward higher frequencies of the stretching band with respect to pure water. We ascribe this effect to a lowering of the molecular dipole moments due to a decrease in the dipole moments of molecules belonging to the first and second solvation shells with respect to bulk water. An analysis of the dipole orientation correlations proves that the screening of solutes is dominated by short-range effects. These jointly experimental and theoretical results are corroborated by the good agreement between calculated and measured dielectric constants of our target solution.

Tautomerism in Reduced Pyrazinacenes

Monoprotic and diprotic NH tautomerism in reduced oligoazaacenes, the pyrazinacenes, was studied by using first principles simulations. Stepwise reductions in the metadynamics-sampled free energy profile were observed during consecutive monoprotic tautomerizations, with energy barriers gradually reducing with increasing proton separation during monoprotic processes. This is accompanied by an increasing contribution from the quinoidal electronic structure, as evidenced by the computed highest occupied molecular orbital (HOMO) structure. An unusual odd-even effect in the free energy profiles is also observed upon changing the length of the pyrazinacene. Calculated HOMO structures reveal an increasing tendency for delocalization of pyrazine lone pairs with an increasing number of ring annelations. The influence of tautomerism on the pyrazine lone pair delocalization was also observed. Tautomers with protons situated centrally on the pyrazinacene backbone are predicted to be more stable due to a combination of (enamine) delocalization and a loss of Clar sextet resonance stabilization in tautomers with protons at terminal pyrazine rings. Experimental evidence suggesting the structure of pyrazinacene tautomers is included and discussed as a support to the calculation.

Evidence for a ball-shaped cyclen cyclophane: an experimental and first principles study.

Conformational isomerism of a ball-shaped cyclophane of cyclen was studied using NMR and computational methods with the most notable conformer containing a highly symmetric cyclic benzene tetramer.

Proton Wires via One-Dimensional Water Chains Adsorbed on Metallic Steps

The process of proton transfer is here analyzed for one-dimensional water chains adsorbed on metallic steps. When the water chain contains a hydronium and a hydroxyl ion, two different mechanisms are possible, depending on the metal substrate. On coinage metals (Ag, Au), recombination is observed through a spontaneous Grotthuss mechanism. On more reactive surfaces (Pd and Pt), the hydronium ion is unstable and releases a proton that adsorbs onto the metal, leaving the negatively charged OH(-) unbalanced. In this case, the negative charge can be transferred along the wire with very low activation barriers.