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Water-Induced Phase Transition in Cyclohexane/n-Hexanol/Triton X-100 Mixtures at a Molar Composition of 1/16/74
Mario E Flores1,2, Francisco Martínez1, Andrés F Olea3
1Departamento de Ciencia de los Materiales, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile , Avenida Tupper 2069, Santiago 8370451, Chile.
Abstract:
Molecular aggregation in a mixture of Triton X-100/n-hexanol/cyclohexane at a molar ratio of 1/16/74 is studied upon addition of small amounts of water. The composition of organic components has been chosen at a ratio n-hexanol/cyclohexane where a well-formed hydrogen bond network has been described. The ratio Triton X-100/n-hexanol has been chosen to afford a stoichiometry of ethylene oxide (EO) residues/n-hexanol of 1/2. At these conditions the addition of water consecutively produces the appearance of three defined phases: a clear solution, a lamellar phase, and a microemulsion. The two corresponding transitions occur at water/EO/n-hexanol molar ratios of 2/1/2 (clear to lamella), and 3/1/2 (lamella to microemulsion), while phase separation occurs at a molar ratio of 4/1/2, highlighting the important role of stoichiometry. Molecular dynamics measured by 1H NMR techniques, such as DOSY, and calculations of T1 and T2 relaxation times allow distinguishing the transition between the different phases and justifying their structure. Molecular assembly in the three phases is organized around hydrogen bond networks in which the hydroxyl groups of both TX-100 and n-hexanol, ethylene oxide groups of TX-100, and water participate. 1D 1H NMR spectral changes correlate with the different characteristics of the different phases. As the main characteristics of the lamellar phase we find a very restricted mobility of the molecules involved, and water chemical shifts in 1D 1H NMR spectra of around 5.0 ppm, higher than that of bulk water appearing at 4.7 ppm.
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Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...

