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th  - 1987 - 51st ENC Conference

th  - 1987 - 51st ENC Conference

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MF9<br />

NMR OF XENON ABSORBED IN SOLID POLYMERS<br />

A PROBE OF THE AMORPHOUS STATE<br />

Thomas R. Stengle<br />

Dept. of Chemistry, Univ. of Massachusetts, Amherst, MA 01003<br />

Kenne<strong>th</strong> L. Williamson*<br />

Dept. of Chemistry, Mount Holyoke College, So. Hadley, MA 01075<br />

Gaseous xenon is readily taken up into <strong>th</strong>e amorphous regions of<br />

solid polymers. In <strong>th</strong>is state <strong>th</strong>e 12eXe spectrum can be easily<br />

obtained. In earlier work we have shown <strong>th</strong>at <strong>th</strong>e 120Xe resonance<br />

is exceptionally sensitive to <strong>th</strong>e nature of its surroundings,<br />

and <strong>th</strong>at it can be used to probe <strong>th</strong>e structure of liquids and<br />

lipid bilayers.1 Here we report on its application to <strong>th</strong>e<br />

amorphous regions of solid polymers. When contained wi<strong>th</strong>in low<br />

density polye<strong>th</strong>ylene, <strong>th</strong>e chemical shift of xenon is ca. 200<br />

ppm downfield from <strong>th</strong>e pure gas. The NMR lines are broad, and<br />

<strong>th</strong>eir shape is especially sensitive to <strong>th</strong>e surrounding<br />

structure. In particular, <strong>th</strong>e glass transition of polye<strong>th</strong>yl-<br />

me<strong>th</strong>acrylate is clearly observed by its effect on bo<strong>th</strong> chemical<br />

shift and lineshape of <strong>th</strong>e xenon signal. The application of<br />

xenon NMR to several polymers will be discussed.<br />

IK. W. Miller, N.V. Reo, A. J. M. Schoot Uiterkamp, D. P.<br />

Stengle, T. R. Stengle and K. L. Wlliamson, Proc. Natl. Acad.<br />

Sci. USA, 78, 4946 (1981).

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