15min:

EMILIO J. COCINERO, Departamento de Química Física, Universidad del País Vasco, 48080 Bilbao, Spain; ALBERTO LESARRI, Departamento de Química Física y Química Inorgánica, Universidad de Valladolid, 47011 Valladolid, Spain; PATRICIA ECIJA, Departamento de Química Física, Universidad del País Vasco, 48080 Bilbao, Spain; JENS-UWE GRABOW, Institut für Physikalische Chemie und Elektrochemie, Gottfried-Wilhelm-Leibniz-Universität Hannover, Callinstraß e 3A, 30167 Hannover, Germany; JOSE A. FERNÁNDEZ, FERNANDO CASTANO, Departamento de Química Física, Universidad del País Vasco, 48080 Bilbao, Spain.

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We report an investigation of the rotational spectrum of several tropane alkaloids using the new Balle-Flygare-type FT-MW spectrometer built at the University of the Basque Country. The initial work focused on the azabicycles of tropinone, scopine and scopoline, vaporized using heating methods. For tropinone the spectrum confirmed the presence of equatorial and axial conformers originated by the inversion of the N -methyl group, with the tropane motif adopting a distorted chair configuration. The determination of substitution and effective structures for the two conformers included the ¹³C, ¹⁵N and ¹⁸O isotopomers observed in natural abundance. The structures revealed the flexibility and structural changes associated to the N -methyl inversion, mostly a flattening at the nitrogen atom and a simultaneous rising of the carbonyl group in the axial form. The investigation of scopine gave an intense spectrum, but it was inconsistent with the structural models expected for this molecule. The carrier of the new spectrum was later identified as scopoline, generated in situ by an intramolecular reaction at the moderate temperatures of the nozzle. A single conformation was detected for scopoline, with an ether bridge seriously distorting the tropane motif.