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MW SYSTEMATIC STUDY OF ALKALOIDS: THE DISTORTED TROPANE OF SCOPOLINE
Patricia Écija Verdejo Spectroscopy Group Faculty of Science and Technology University of the Basque Country
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Introduction TROPANE ALKALOIDS Solanacease Erythrocylacease tropane 2
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Why are the tropane alkaloids interesting?
Introduction Why are the tropane alkaloids interesting? PHARMACOLOGICAL USES ANTICHOLINERGIC Scopolamine NEUROSTIMULANTS Cocaine NEUROTRANSMISSION EXPERIMENTS Phenyltropane STRUCTURE-ACTIVITY INTERACT with other compounds NEW PHARMACOLOGICAL compounds 3
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Rotational Spectroscopy
Introduction Rotational Spectroscopy in Supersonic jets Tropane Alkaloids Theoretical Calculations ab initio – MP2 DFT methods – B3LYP / M062X 4
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TROPANE ALKALOIDS Introduction TROPINONE X-Ray Difraction Axial
2 kJ mol-1 X-Ray Difraction Axial NMR Axial/equatorial MW Spectroscopy PCCP, 12, 6076, 2010 Kristallogr. NCS, 222, 225, 2007 A.S.J. Org. Chem., 53, 2172, 1988 EPOXYTROPANES SCOPINE 5
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Experimental Set Up Scopine 97% 4-18 GHz PCCP, 12, 12486, 2010
~ cm-1 Resolution: kHz
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Decomposition Products
Results Scopine Decomposition Products Scopine ---- Ne Scopine ---- H2O Reaction Product Scopine Scopine Scopoline Chem. Phys. Chem., DOI: /cphc , 2013
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Rotational Parameters of Scopoline
Results Rotational Parameters of Scopoline Chem. Phys. Chem., DOI: /cphc , 2013
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Results No tunnel splitting >11.4 kJ mol-1 11.8 kJ mol-1 (MP2)
Chem. Phys. Chem., DOI: /cphc , 2013
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IS LASER VAPORIZATION THE SOLUTION?
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FT-MW Ablation 355 nm Nd-YAG laser ca. 2-3 mJ/pulse ~0.0000001 cm-1
Resolution: kHz PCCP, 12, 12486, 2010
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Results SCOPINE
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Rotational Parameters of Scopine
Results Rotational Parameters of Scopine
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Results Tunnel splitting 6.25 (1) kJ mol-1 5.99 kJ mol-1 (MP2)
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Conclusion SCOPINE SCOPOLINE SCOPINE STRUCTURAL TUNNEL SPLITTING
N-Methyl group EQUATORIAL STRUCTURAL ISOMERIZATION N-Methyl group AXIAL SCOPINE C3 C6 SCOPOLINE SCOPINE Chem. Phys. Chem., DOI: /cphc , 2013
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Acknowledgements MW Spectroscopy Group Collaborators
Dr. Emilio José Cocinero Montse Vallejo Estíbaliz Méndez Dr. José A. Fernández Dr. Francisco J. Basterretxea Prof. Fernando Castaño Collaborators Prof. Alberto Lesarri Prof. Jens-Uwe Grabow Prof. Walther Caminati Prof. Brooks Pate 16
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