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Título

Static and dynamic properties of 1,1-Bi-2-naphthol and its conjugated acids and bases

Autor Alkorta, Ibon ; Cancedda, Celine; Cocinero, Emilio José; Dávalos, J.Z. ; Écija, Patricia; Elguero, José ; González, Javier; Lesarri, Alberto; Ramos, Rocio; Reviriego, Felipe ; Roussel, Christian; Uriarte, Iciar; Vanthuyne, Nicolas
Palabras clave Density
Binaphthol
Functional calculations
Rotational spectroscopy
Atropisomerism
Acidity
Fecha de publicación 2014
EditorJohn Wiley & Sons
Citación Chemistry - A European Journal 20: 14816- 14825 (2014)
ResumenSeveral convergent techniques were used to characterize 1,1′-bi-2-naphthol (BINOL) and some of its properties. Its acidity in the gas-phase, from neutral species to monoanion, was measured by mass spectrometry. The conformation and structure of BINOL in the gas phase was determined by microwave rotational spectroscopy. NMR experiments in fluorosulfonic acid established that BINOL was monoprotonated on one of the hydroxyl oxygen atoms. The enantiomerization barriers reported in the literature for BINOL under neutral, basic, and acid conditions were analyzed with regard to the species involved. Finally, DFT calculations allowed all of these results to be gathered in a coherent picture of the BINOL structure.
URI http://hdl.handle.net/10261/109402
DOI10.1002/chem.201402686
Identificadoresdoi: 10.1002/chem.201402686
issn: 0947-6539
e-issn: 1521-3765
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