Supporting Information
| Supporting Information File 1: NMR spectra of compounds 2 and 5; fluorimetric titrations of 2 with acid and CB[7]; determination of 0-0 transition energies; analysis of binding isotherms from photometric titrations of 2 with CB[7]. | ||
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Cite the Following Article
Interactions between photoacidic 3-hydroxynaphtho[1,2-b]quinolizinium and cucurbit[7]uril: Influence on acidity in the ground and excited state
Jonas Becher, Daria V. Berdnikova, Darinka Dzubiel, Heiko Ihmels and Phil M. Pithan
Beilstein J. Org. Chem. 2017, 13, 203–212.
https://doi.org/10.3762/bjoc.13.23
How to Cite
Becher, J.; Berdnikova, D. V.; Dzubiel, D.; Ihmels, H.; Pithan, P. M. Beilstein J. Org. Chem. 2017, 13, 203–212. doi:10.3762/bjoc.13.23
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- Bosch, P.; Sucunza, D.; Mendicuti, F.; Domingo, A.; Vaquero, J. J. Dibenzopyridoimidazocinnolinium cations: a new family of light-up fluorescent DNA probes. Organic Chemistry Frontiers 2018, 5, 1916–1927. doi:10.1039/c8qo00236c
- Macartney, D. H. Cucurbit[n]uril Host‐Guest Complexes of Acids, Photoacids, and Super Photoacids. Israel Journal of Chemistry 2017, 58, 230–243. doi:10.1002/ijch.201700096
