The structure of the title compound (C17H15N3O4S)2 the schiff base, bis(N-(5-methyl-3-isoxazolyl)-4-[(2-hydroxy benzylidene)-amino]) benzene sulfonamide was elucidated by H1, C13 NMR, UV-VIS and IR spectroscopic techniques. The X-ray structure was determined in order to establish the conformation of the molecule. The compound crystallizes in the triclinic space group P-1, with a = 11.419(1), b = 11.426(0), c = 13.316(1) A° , ±= 71.94(2), ²= 89.79(1), ³= 89.14(2)° and Z = 4. Two benzene rings and azomethine group are practically coplanar, as a result of intramolecular hydrogen bonds involving the hydroxy O atom and azomethine N atom. The component species further interact via N-H...N and C-H...O hydrogen bonds and À-À stacking interactions.

Synthesis and Crystal Structure of a New Schiff Base 4-[(2-hydroxy-benzylidene)-amino]-N-(5-methyl-isoxazol-3-yl)-benzenesulfonamide

Bocelli G;Cantoni A
2009

Abstract

The structure of the title compound (C17H15N3O4S)2 the schiff base, bis(N-(5-methyl-3-isoxazolyl)-4-[(2-hydroxy benzylidene)-amino]) benzene sulfonamide was elucidated by H1, C13 NMR, UV-VIS and IR spectroscopic techniques. The X-ray structure was determined in order to establish the conformation of the molecule. The compound crystallizes in the triclinic space group P-1, with a = 11.419(1), b = 11.426(0), c = 13.316(1) A° , ±= 71.94(2), ²= 89.79(1), ³= 89.14(2)° and Z = 4. Two benzene rings and azomethine group are practically coplanar, as a result of intramolecular hydrogen bonds involving the hydroxy O atom and azomethine N atom. The component species further interact via N-H...N and C-H...O hydrogen bonds and À-À stacking interactions.
2009
Istituto dei Materiali per l'Elettronica ed il Magnetismo - IMEM
Synthesis and characterization
Schiff base Spectral studies and À- À interactions. Schiff base Spectral studies and p- p interactions
Synthesis and characterization
X-ray diffraction
Spectral studies and À- À interactions. Spectral studies and p- p interactions
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/41115
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