Abstract
We present a study of the microscopic dynamics of water trapped in reverse non-ionic micelles by means of a series of molecular dynamics simulations. The analysis of the effects of micellar confinement on spectroscopical properties of an excess proton has also been considered. Our micelles were microemulsions made with the neutral surfactant diethylene glycol monodecyl ether [CH(3)(CH(2))(11)(OC(2)H(4))(2)OH]. Simulation experiments including the proton species were performed using a multistate empirical valence bond Hamiltonian model. Diffusion of water in the micelle is markedly slower than that in the bulk liquid, in the same fashion as happens with reorientational dynamics. Spectral densities of hydrogens revealed a blue-shift of the OH-stretching vibration together with a split of the main band into two components. Absorption lineshapes of the solvated proton in the vicinity of the internal surface of the micelle indicate the coexistence of Eigen-like and Zundel-like structures and a tendency to red-shifting (compared to the aqueous unconstrained excess proton case) of the two relevant spectral bands (around 2000 and 2500 wavenumbers) mainly due to the slower dynamics of proton vibrations in water near interfaces.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
