Abstract
Average molecular optical anisotropies ‹γ2› of the three stereoisomers of 2,4,6-triphenylheptane were measured by depolarized Rayleigh scattering. Analysis of these results led to the determination of the relative stability among the various conformational structures of these isomers.
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G. Fourche and M. T. Jacq, Polym. J, 4, 465 (1973).
G. Fourche and B. Lemaire, Polym. J., 4, 476 (1973).
P. Bothorel, J. Colloid Interface Sci., 27, 529 (1968).
H. Pivcova, M. Kolinsky, D. Lim, and B. Schneider, J. Polym. Sci., Part C, 22, 1093 (1969).
A. E. Tonelli, Y. Abe, and P. J. Flory, Macromolecules, 3, 803 (1970).
P. J. Flory, “Statistical mechanics of chain molecules,” Interscience, New York, N.Y., 1969.
B. Jasse, Results not published.
F. A. Bovey, F. P. Hood, E. W. Anderson, and L. C. Snyder, J. Chem. Phys., 42, 3900 (1965).
B. Jasse and L. Monnerie, J. Phys. D, Appl. Phys., 8, 863 (1975).
A. D. Williams and P. J. Flory, J. Am. Chem. Soc., 91, 3111 (1969).
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Fourche, G., Jasse, B. & Maelstaf, P. Conformational Analysis of Stereoisomers of Triphenylheptane by Depolarized Rayleigh Scattering. Polym J 9, 537–539 (1977). https://doi.org/10.1295/polymj.9.537
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DOI: https://doi.org/10.1295/polymj.9.537