Chain dynamics of bilayer n-decylammonium chloride studied by deuteron NMR spectroscopy
- 27 Downloads
- 13 Citations
Abstract
N-decylammonium chloride is a polymorphic solid which exhibits a variety of layered phases. The molecular dynamics and phase transitions in these phases have been studied using2H NMR of selectively deuterated n-decylammonium in the chain positions 1 and 6 and in the ammonium group. Measurements were performed over the temperature range of the interdigitated phase I, the non-interdigitated monoclinic phase δ, the tetragonal phase α, and the monotropic phase ε, obtained upon cooling the sample from the α-phase. In phase I, below 321 K, the hydrocarbon chain is rigid except for ND3 rotation about its own symmetry axis. In phase δ, between 321 K and 325 K, a fast motion of the hydrocarbon chains is assigned to an exchange between two pairwise nonequivalent positions. The chains are slightly tilted in this phase. In phase α above 325 K the chains rotate freely around their long axes experiencing additional transgauche conformational dynamics. In the non-interdigitated phase ε the spectra can be interpreted by assuming a reorientation between two variously occupied potential wells about the axis determined by the C-N bond, which is believed to be parallel to the normal bilayer axis.
Keywords
Phase Transition Molecular Dynamic Symmetry Axis Hydrocarbon Chain Tetragonal PhasePreview
Unable to display preview. Download preview PDF.
References
- 1.Sackmann, E.: Ber. Bunsenges. Phys. Chem.82, 891 (1978); Sackmann, E.: Physical basis of trigger processes and membrane structures. Biological membranes. Vol. 5. London: Academic Press 1984Google Scholar
- 2.Ringsdorf, H., Schlarb, B., Venzmer, J.: Angew. Chem.100, 117 (1988); Amey, R.L., Chapman, D.: Infared spectroscopic studies of model and natural biomembranes. Biomembrane structure and function. p. 199. Weinheim: Verlag Chemie 1984Google Scholar
- 3.Kind, R., Blinc, R., Arend, H., Muralt, P., Slak, J., Chapuis, G., Schenk, K.J.: Phys. Rev. A26, 1816 (1982)Google Scholar
- 4.Kind, R., Plesko, S., Arend, H., Blinc, R., Zeks, B., Seliger, J., Lozar, B., Slak, J., Levstik, A., Filipic, C., Zagar, V., Lahajnar, G., Milia, F., Chapuis, G.: J. Chem. Phys.71, 2118 (1979)Google Scholar
- 5.Chapuis, G., Schenk, K., Zuniga, J.: Mol. Cryst. Liq. Cryst.113, 113 (1984)Google Scholar
- 6.Chapman, D.: Q. Rev. Biophys.8, 185 (1975)Google Scholar
- 7.Seliger, J., Zagar, V., Blinc, R., Kind, R., Arend, H., Chapuis, G., Schenk, K.J., Milia, F.: Z. Phys. B — Condensed Matter69, 379 (1987)Google Scholar
- 8.Seliger, J., Zagar, V., Blinc, R., Arend, H., Chapuis, G.: J. Chem. Phys.78, 2661 (1983)Google Scholar
- 9.Davies, J.H., Jeffrey, K.R., Bloom, M., Valic, M.I., Higgs, T.P.: Chem. Phys. Lett.42, 390 (1976)Google Scholar
- 10.Abragam, A.: The principles of nuclear magnetism. London: Oxford University Press 1961Google Scholar
- 11.Hunt, M.J., Mackey, A.L.: J. Magn. Reson.15, 402 (1974)Google Scholar
- 12.Spiess, H.W.: Adv. Polym. Sci.66, 23 (1985)Google Scholar
- 13.Rosenke, K., Sillescu, H., Spiess, H.W.: Polymer21, 757 (1980)Google Scholar
- 14.Flory, P.J.: Statistical mechanics of chain molecules. New York: Wiley Interscience 1969Google Scholar
- 15.Hirschinger, J., Miura, H., Gardner, K.H., English, A.D.: Macromolecules23, 2153 (1990)Google Scholar