1991
DOI: 10.1021/ja00008a005
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Twisted intramolecular charge-transfer fluorescence of aromatic amides: conformation of the amide bonds in excited states

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Cited by 122 publications
(83 citation statements)
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“…This dependence was proved by other authors [14,15]. The T value obtained for I in MCH at room temperature and at 77 K is in good agreement with the results of [16] and [17].…”
Section: Discussionsupporting
confidence: 89%
“…This dependence was proved by other authors [14,15]. The T value obtained for I in MCH at room temperature and at 77 K is in good agreement with the results of [16] and [17].…”
Section: Discussionsupporting
confidence: 89%
“…Thus, the major isomer of 2 A (racemate and enantiomers) exists in a cis arrangement in solution as well as in the solid state. This is consistent with the report [13] that N-benzoyl-N-methylanilines exist in a cis structure. Similar structural features were observed for 2 B, 3 A, 3 B, 4 A, and 4 B as for 2 A.…”
supporting
confidence: 94%
“…9 N-Methylation of aromatic amides and ureas has been proposed as a general strategy for control of conformation about the C-N bonds of such compounds, since it leads to structures in which close Ar-Ar contacts are prevalent. [10][11][12][13] However, little detailed work has been reported on the conformational preferences of simple mono-ureas, despite the fact that the helicity of an oligourea is dependent on the adoption by each individual urea linkage of a well-defined local conformation.…”
Section: Introductionmentioning
confidence: 99%