The rotational spectra of the most stable conformer of tryptophol has been assigned by free jet millimeter-wave absorption spectroscopy. The molecule is stabilized by an intramolecular N–H p bridge, formed between the hydroxyl hydrogen and the p system of the pyrrol unity.
R. Sanchez, W. Caminati, J.C. López, J.L. Alonso (2005). The rotational spectra of conformers of biomolecules: Tryptophol. CHEMICAL PHYSICS LETTERS, 414, 226-229 [10.1016/j.cplett.2005.08.071].
The rotational spectra of conformers of biomolecules: Tryptophol
CAMINATI, WALTHER;
2005
Abstract
The rotational spectra of the most stable conformer of tryptophol has been assigned by free jet millimeter-wave absorption spectroscopy. The molecule is stabilized by an intramolecular N–H p bridge, formed between the hydroxyl hydrogen and the p system of the pyrrol unity.File in questo prodotto:
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