Asma and Balakrishna, K. and Yathirajan, H. S. and Rathore, Ravindranath S. and Glidewell, Christopher (2018) Four 1-aryl-1H-pyrazole-3,4-dicarboxylate derivatives: synthesis, molecular conformation and hydrogen bonding. Acta Crystallographica Section E, 74 (12). pp. 1783-1789. ISSN 1600-5368
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Abstract
Four 1-aryl-1H-pyrazole-3,4-dicarboxylate derivatives, one acid, two esters and a dicarbohydrazide have been synthesized starting from 3-aryl sydnones, and structurally characterized. There is an intramolecular O—H⋯O hydrogen bond in 1-phenyl-1H-pyrazole-3,4-dicarboxylic acid, C11H8N2O4, (I), and the molecules are linked into a three-dimensional framework structure by a combination of O—H⋯O, O—H⋯N, C—H⋯O and C—H⋯π(arene) hydrogen bonds. In each of the two esters dimethyl 1-phenyl-1H-pyrazole-3,4-dicarboxylate, C13H12N2O4, (II), and dimethyl 1-(4-methylphenyl)-1H-pyrazole-3,4-dicarboxylate, C14H14N2O4, (III), C—H⋯O hydrogen bonds lead to the formation of cyclic centrosymmetric dimers: in (III), one of the methoxycarbonyl groups is disordered over two sets of atomic sites having occupancies 0.71 (2) and 0.29 (2). An intramolecular N—H⋯O hydrogen bond is present in the structure of 1-(4-methoxyphenyl)-1H-pyrazole-3,4-dicarbohydrazide, C12H14N6O3, (IV), and the molecules are linked into a three-dimensional framework structure by a combination of N—H⋯O, N—H⋯N, N—H⋯π(arene) and C—H⋯O hydrogen bonds. Comparisons are made with the structures of a number of related compounds.
Item Type: | Article |
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Uncontrolled Keywords: | synthesis, 1,3-dipolar addition, crystal structure, molecular conformation, disorder, hydrogen bonding, supramolecular assembly |
Subjects: | C Chemical Science > Chemistry |
Divisions: | Department of > Chemistry |
Depositing User: | C Swapna Library Assistant |
Date Deposited: | 12 Oct 2019 07:34 |
Last Modified: | 12 Oct 2019 07:34 |
URI: | http://eprints.uni-mysore.ac.in/id/eprint/8943 |
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