Protonation, Tautomerization and Valence Tautomerization of Selected Imidazo[4,5-F]Quinolines - a Theoretical-Study of Gas and Liquid Basicity of Imidazo[4,5-F]Quinolines

Autor: Öğretir, Cemil, Kanışkan, Nevin
Přispěvatelé: Anadolu Üniversitesi, Kanışkan, Nevin
Jazyk: angličtina
Rok vydání: 1993
Popis: WOS: A1993KR85900020
The theoretical calculations on imidazo[4,5-f] quinolines has shown that the first protonation takes place at the pyridine nitrogen atom rather than at the imidazole nitrogen atom. The preferred tautomeric form was found to be the 3H form. A satisfactory correlation between experimentally obtained pK(a) values and computed electron densities and energies was found.
Databáze: OpenAIRE