Chlorodifluoroacetyl azide, ClF 2CC(O)N 3: Preparation, properties, and decomposition

Chlorodifluoroacetyl azide, ClF 2CC(O)N 3, was prepared and characterized by IR (gas, Ar matrix), Raman (liquid), UV-vis (gas), and 19F, 13C NMR spectroscopy. The vibrational spectra were analyzed in terms of a single conformer, gauche-syn, where the Cl-C and the N α=N β bonds are gauche and syn to...

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Detalles Bibliográficos
Autores: Ramos Guerrero, Luis Alejandro, Zeng, Xiaoqing, Ulic, Sonia Elizabeth, Beckers, Helmut, Willner, Helge, Della Védova, Carlos Omar
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2012
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/82301
Acceso en línea:http://hdl.handle.net/11336/82301
Access Level:acceso abierto
Palabra clave:Clorodifluoroacetyl Azide
Clf2cc(O)N3
Preparation And Properties
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Descripción
Sumario:Chlorodifluoroacetyl azide, ClF 2CC(O)N 3, was prepared and characterized by IR (gas, Ar matrix), Raman (liquid), UV-vis (gas), and 19F, 13C NMR spectroscopy. The vibrational spectra were analyzed in terms of a single conformer, gauche-syn, where the Cl-C and the N α=N β bonds are gauche and syn to the C=O bond, respectively. The photo and thermal decomposition reactions of the azide were studied with the aid of matrix isolation. In both cases, a new isocyanate species ClF 2CNCO was produced and characterized by matrix IR spectroscopy. The conformational properties and the Curtius rearrangement pathways of this new carbonyl azide were theoretically explored, which suggest the preference of a concerted over stepwise decomposition for the global minimum gauche-syn conformer.