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Synthesis of 1,3-Diphenyl-2,8-dihydrodibenz[e,h]-azulene-2,8-dione

โœ Scribed by Prof. Dr. W. Ried; Dipl.-Chem. J. Ehret


Publisher
John Wiley and Sons
Year
1968
Tongue
English
Weight
196 KB
Volume
7
Category
Article
ISSN
0044-8249

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โœฆ Synopsis


Solutions of (4j in organic solvents display an intensive blue fluorescence and in aqueous mineral acids a blue-green fluorescence. In the N M R spectrum (CDC13) a singlet occurs at T = 0.87, which is ascribed to the protons H-1 and H-3 (the neighboring protons to the ring nitrogen); the remaining protons show a characteristic split multiplet with main signals at T = 2.05, 2.18, 2.38, and 2.50. In trifluoroacetic acid ( 4 ) is protonated and H-1 and H-3 give rise to a doublet, J = 6 Hz, atT = 0.53. The multiplet of the remaining ring protons occurs well downfield at


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