Methyl dynamics flattens barrier to proton transfer in crystalline tetraacetylethane.

We analyze the interplay between proton transfer in the hydrogen-bond bridge, O···H···O, and lattice dynamics in the model system tetraacetylethane (TAE) (CH(3)CO)(2)CH═CH(COCH(3))(2) using density functional theory. Lattice dynamics calculations and molecular dynamics simulations are validated against neutron scattering data. Hindrance to the cooperative reorientation of neighboring methyl groups at low temperatures gives a preferred O atom for the bridging proton.

"Hexagonal molybdenum trioxide"--known for 100 years and still a fount of new discoveries.

In 1906, the preparation of “molybdic acid hydrate” was published by Arthur Rosenheim. Over the past 40 years, a multitude of isostructural compounds, which exist within a wide phase range of the system MoO3−NH3−H2O, have been published. The reported molecular formulas of “hexagonal molybdenum oxide” varied from MoO3 to MoO3·0.