15min:

C. J. TAINTER, J. L. SKINNER, Theoretical Chemistry Institute and Department of Chemistry, University of Wisconsin, Madison, WI 53706.

We use a newly developed and recently reparameterized classical empirical simulation model for water that involves explicit three-body interactions to study the water hexamer. The lowest energy isomer is found to be one of the cage structures, in agreement with vibration-rotation-tunneling experiments. Furthermore, the relative energy ordering of the different isomers is in good agreement with CCSD(T) calculations. The OH-stretch spectra calculated for the low-energy structures is compared to ab initio and density functional theory calculations. Finally, replica-exchange molecular dynamics were performed from 40 to 194 K, showing the cage isomer has the lowest free energy from 0 to 70 K, and the book isomer has the lowest free energy from 70 to 194 K. The OH-stretch spectra were calculated from these simulations, leading to a re-assignment of the peaks in recent experimental spectra.