ArticleJournal of fluorescence2014
Solvatoemissive dual fluorescence of N-(pyridylmethyl)-3-nitro-1,8-naphthalimides.
Article in Journal of fluorescence, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
2 authors.
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Abstract
Solvatoemissive dual fluorescence emission observed in the three positional isomers of N-(n-pyridylmethyl)-3-nitro-1,8-naphthalimide [n = 2 (1), 3 (2), 4 (3)] are described. Dual fluorescence emission in this class of compounds occurs from the excited states with extended conjugation via π-stacking interactions. The crystal structure of the compound 1 and the chloride salt of 2 were determined. The compound 1 forms dimeric assemblies through π-stacking interactions. Whereas the structure of the chloride salt of 2 is composed of dimeric assemblies of the cationic part which hold cyclic hydrated anionic assemblies through weak C-H(…)Cl interactions. Anionic hydrated assemblies between water and chloride ions have cyclic tetrameric structure through O-H(…)Cl interactions.
Identifiers
24510429What OpenQuestion holds
Registered trials
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