Adiabatic ring opening in tethered naphthalene and anthracene cycloadducts

The cycloadducts of tethered naphthalene and anthracene derivatives undergo photochemical ring opening to an electronically excited product with adiabatic yields up to 90%.

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Veröffentlicht in:Photochemical & photobiological sciences 2010-08, Vol.9 (8), p.1082-1084
Hauptverfasser: Sundaresan, Arun Kumar, Jockusch, Steffen, Li, Yongjun, Lancaster, Jeffrey R., Banik, Steven, Zimmerman, Paul, Blackwell, James M., Bristol, Robert, Turro, Nicholas J.
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Sprache:eng
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Zusammenfassung:The cycloadducts of tethered naphthalene and anthracene derivatives undergo photochemical ring opening to an electronically excited product with adiabatic yields up to 90%.
ISSN:1474-905X
1474-9092
DOI:10.1039/c0pp00096e