Chemical shift assignments in 1H nmr spectra of four tricarbocyanines have been made. Studies by 1H nmr have shown a rapid acid‐catalyzed proton exchange at positions 1′,7′ and a much slower exchange at positions 3′,5′ of the heptamethine chain. Base catalysis results in a slow exchange at positions 1′,7′ only. Copyright © 1993 Journal of Heterocyclic Chemistry
CITATION STYLE
Lipowska, M., Patterson, S. E., Patonay, G., & Strekowski, L. (1993). A highly selective hydrogen‐deuterium exchange in indolium heptamethine cyanines. Journal of Heterocyclic Chemistry, 30(5), 1177–1180. https://doi.org/10.1002/jhet.5570300503
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