JOURNAL of the Tunisian Chemical Society

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Préparation et structure cristalline du 1,4,7,10,13-benzopentaoxacyclopentadecin-2,3,5,6,8,9,11,12-octahydro-15,16-dinitro

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The synthesis of 1,4,7,10,13- BenzopentaoxacycIopentadecin-2,3,5,6,8,9,11,12-octahydro-15,16-dinitro is achieved by the nitration of 1,4,7,10,13-benzopentaoxacyclodecin-2,3,5,6,8,9,11,12-octahydro. This compound is characterized by spectroscopic technics, IR, UV, 1H-NMR, 13C-NMR, mass spectrometry and by XR diffraction. A monocrystal from the product was selected and its crystal structure solved. The solid crystallizes in the monoclinic system with space group P21/n and a := 11,7443 (3) ; b = 8,5135 (3) ; c = 17,4845(5) Å ; β = 108,324 (1 )° and Z = 4. The cavities of the macrocycle are rigidified by five intramolecular hydrogen bonds, whereas six hydrogen bonds between a molecule and three near neighbors ensure crystal cohesion.

A. Ouerghi, A. Ben Hadj Amor, J. Marrot, F. Meganem

Dinitrobenzo-15-crown-5, crystal structure of C14H18N2O9

Pages 189-194

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