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The Synthesis and Physical Properties of Novel Polyaromatic Profluorescent Isoindoline Nitroxide Probes (Eur. J. Org. Chem. 32/2008)
Author(s) -
FairfullSmith Kathryn E.,
Bottle Steven E.
Publication year - 2008
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200890087
Subject(s) - nitroxide mediated radical polymerization , chemistry , isoindoline , photochemistry , fluorescence , fluorophore , radical polymerization , organic chemistry , polymerization , polymer , optics , physics
The cover picture shows the minimal fluorescence emitted from a nitroxide‐quenched diphenylanthracene fluorophore (left‐hand side) and the contrasting strongly fluorescent result after the spin of the nitroxide radical has been removed by reduction or radical trapping (second from left). The same differential can be seen for the acetylene‐extended system. The top right of the picture shows the same four flasks viewed in visible light. Details are discussed in the article by K. E. Fairfull‐Smith and S. E. Bottle on p. 5391 ff. Photo courtesy of Dr. Aaron Micallef, AIBN, University of Queensland, Australia.