1936
DOI: 10.1007/bf01518851
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Die Ultraviolettabsorption einiger aromatischer Kohlenwasserstoffe

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Cited by 7 publications
(3 citation statements)
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“…The olefins thus confirmed by their production were cis-and frarzs-l-phenylpropenes,39"42 cisand trans-3methyl-l-phenyl-l-butenes,39 cis-and trons-3,3-dimethyl-lphenyl-1-butenes,39 2-methyl-l-phenylpropene,40,43 2-methyl-1,1 -diphenylpropene,44 cts-stilbene,45 trarzs-stilbene,46"47 and pnitrostyrene. 48 The last olefin [mp 26-27 °C (lit.9,48 mp 29 °C)] had a tendency to polymerize in a concentrated solution, but the presently applied conditions for 9 (1.1 X 10"3 mol/L in the presence of TMEDA) allowed us to observe the quantitative formation of the styrene.…”
Section: Methodsmentioning
confidence: 99%
“…The olefins thus confirmed by their production were cis-and frarzs-l-phenylpropenes,39"42 cisand trans-3methyl-l-phenyl-l-butenes,39 cis-and trons-3,3-dimethyl-lphenyl-1-butenes,39 2-methyl-l-phenylpropene,40,43 2-methyl-1,1 -diphenylpropene,44 cts-stilbene,45 trarzs-stilbene,46"47 and pnitrostyrene. 48 The last olefin [mp 26-27 °C (lit.9,48 mp 29 °C)] had a tendency to polymerize in a concentrated solution, but the presently applied conditions for 9 (1.1 X 10"3 mol/L in the presence of TMEDA) allowed us to observe the quantitative formation of the styrene.…”
Section: Methodsmentioning
confidence: 99%
“…The effect of conjugation of the side-chain double bond with the naphthalene ring is less marked than its influence on the benzene chromophore; it may be noted that the conjugated compound shows no fine structure. Closure of the side chain to form a ring, as in 7-methylperinaphthene (67,236) (XXXVIII), leads to a 197); -, 1-allylnaphthalene in ethanol as solvent (193);----, 1-methylnaphthalene in ethanol as solvent (193).…”
Section: Diphenylmentioning
confidence: 99%
“…Ultraviolet absorption spectra. -,1-propenylnaphthalene in ethanol as solvent(197); -, 1-allylnaphthalene in ethanol as solvent(193);----, 1-methylnaphtha-…”
mentioning
confidence: 99%