Conformational analysis in 2,4-dinitrophenol by nuclear Overhauser effect experiments

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The cis conformation of the hydroxyl with respect to the nitro group in 2,4-dinitrophenol under fast exchange conditions and the consequent persistence of the intramolecular hydrogen bond are determined. These facts emerge from the existence of a scalar-coupling-of-the-first-kind relaxation interact...

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Detalles Bibliográficos
Autores principales:	Balonga, P.E., Vásquez, C., Contreras, R.H., Kowalewski, V.J., de Kowalewski, D.G.
Formato:	JOUR
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_00222364_v59_n1_p58_Balonga
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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