CEQUINOR   05415
CENTRO DE QUIMICA INORGANICA "DR. PEDRO J. AYMONINO"
Unidad Ejecutora - UE
artículos
Título:
Spectroscopic and theoretical study of 2-acetylphenyl-2-naphthoate
Autor/es:
GABRIEL S. SUAREZ; NÉSTOR E. MASSA; ALICIA H. JUBERT; JORGE L. JIOS; JUAN C. AUTINO; GUSTAVO P. ROMANELLI.
Revista:
SPECTROCHIMICA ACTA. PART A, MOLECULAR AND BIOMOLECULAR SPECTROSCOPY.
Editorial:
Elsevier
Referencias:
Lugar: New York; Año: 2009 vol. 71 p. 1989 - 1989
ISSN:
1386-1425
Resumen:
Mid-, far-infrared, and Raman vibrational spectra of 2-acetylphenyl 2-naphthoate have been measured at room and low temperatures. The molecule was also analyzed by means of ab initio calculations. The conformational space has been scanned using molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps ab initio calculations. The conformational space has been scanned using molecular dynamics and complemented with functional density calculations that optimize the geometry of the lowest-energy conformers 2-acetylphenyl 2-naphthoate. The vibrational frequencies and the 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps 1H and 13C NMR chemical shifts were assigned using functional density calculations and theoretically compared with the experimental ones. We also calculated and analyzed the corresponding molecular electrostatic potential maps