Journal
ADVANCED MATERIALS
Volume 16, Issue 7, Pages 636-+Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.200305792
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Diarylethene derivatives with two chiral substituents (see Figure) undergo reversible diastereoselective photocyclization reactions in a bulk amorphous state. An enrichment of one of the diastereomers (25% d.e.) has been found to exist below the glass transition temperature. The diastereoselection clearly indicates that short distance regularity exists in the glassy state.
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