
doi: 10.1021/jp202063m
pmid: 21671648
Photo-retro-Diels-Alder (PrDA) reactions of a variety of Diels-Alder (DA) adducts were studied. Experimental results showed that the photoreactivity (quantum yield) depends on the electron-donating ability of the diene component and the electron-withdrawing ability of the dienophile component. The mechanism was studied by trapping the reaction intermediate, O(2) quenching, time-resolved absorption, and fluorescence spectroscopy. All the results support a mechanism that involves a charge-separated intermediate generated from a singlet excited state. The PrDA reaction may find applications in photoresponsive materials, photolithography, drug delivery, and mechanistic research.
PENTACENE PRECURSOR, DERIVATIVES, Physics, CYCLOREVERSION, ANTHRACENE, Atomic, Molecular & Chemical, POLYACETYLENE, Chemistry, ROUTE, Physical, THIN-FILM TRANSISTORS, DIENOPHILES
PENTACENE PRECURSOR, DERIVATIVES, Physics, CYCLOREVERSION, ANTHRACENE, Atomic, Molecular & Chemical, POLYACETYLENE, Chemistry, ROUTE, Physical, THIN-FILM TRANSISTORS, DIENOPHILES
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