SYNTHESIS AND CHARACTERIZATION NMR 1D AND 2D OF THE SULPHURATED DERIVATIVES OF THE 1-PHENYL- 3-METHYL-2-PIRAZOLINE-5-ONA AND THEIR LIGAND POTENCIAL CAPACITY

  • Sergio Zamorano Autor
  • Juan Camus Autor
DOI: https://doi.org/10.37761/rsqp.v81i1.7
Keywords: Pyrazoline derivatives, 1D and 2D NMR spectroscopy

Abstract

In this work the result of the synthesis of the 4- hexil-dithiocarboxilate-1-phenil-3-methyl-
2-pirazolin-5-ona(PirC6), and 4-dithiocarboxilate of dodecil-1-phenil-3-methyl-2-pirazolin-
5-ona(PirC12), is presented and the products are characterized, using the microanalysis ,
the infrared spectroscopy, the spectroscopy of NMR of H1 and C13 and the NMR in two
dimensions (HSQC and HMBC), in order to determine their structures. In addition, the
ligand potential capacity of these products are studied in order to produce coordination
compounds with the uranil (UO2
2+).

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Author Biographies

Sergio Zamorano, Autor

Facultad de Ciencias Naturales y Exactas. Universidad de Playa Ancha, Carvallo Nº270, Playa Ancha,
Valparaíso, Chile

Juan Camus, Autor

Faculty of Natural and Exact Sciences. University of Playa Ancha, Carvallo Nº270, Playa Ancha,
Valparaíso, Chile

Published
2015-03-31
Issue
Vol. 81 No. 1 (2015): Journal of the Chemical Society of Peru
Section
Artículos

Copyright (c) 2015 Sociedad Química del Perú

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This work is licensed under a Creative Commons Attribution 4.0 International License.

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