The effect of hydrophobic-lipophilic interactions on chemical reactivity. 8. Large-ring intramolecular excimer formation brought about by hydrophobic forces
- 1 September 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 109 (19) , 5862-5864
- https://doi.org/10.1021/ja00253a055
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- A microscopic hydrophobicity parameterJournal of the American Chemical Society, 1986
- Effect of hydrophobic-lipophilic interactions on chemical reactivity. 6. The first example of correlation of hydrophobic-lipophilic substituent constants with chemical reactivity for a simple substrate-solvent systemJournal of the American Chemical Society, 1985
- The effect of hydrophobic-lipophilic interactions on chemical reactivity. 4. A case of 17-membered-ring "neighboring-group" participation: compelling evidence for self-coilingJournal of the American Chemical Society, 1984
- Intramolecular excimer formation with 1,3-di(1-pyrenyl)propane. Decay parameters and influence of viscosityJournal of the American Chemical Society, 1984