Now showing items 1-7 of 7
| Abstract: | In the title molecule, C16H11N5, the mean planes of the quinoxaline and indazole fragments form a dihedral angle of 10.62 (5). In the crystal, weak intermolecular N—H..........N hydrogen bonds link the molecules into zigzag chains extending in the [001] direction. The crystal packing also exhibits pye interactions [centroid–centroid distances of 3.7080 (2) and 3.8220 (5) A ˚ ], which form stacks of the molecules parallel to the a axis |
| URI: | http://dyuthi.cusat.ac.in/purl/1649 |
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| leeju.pdf | (199.0Kb) |
| Abstract: | In the molecule of the title compound, C20H16N6, the central C—C bond lies on a crystallographic inversion centre. The quinoxalidine ring is nearly planar, with a maximum deviation of 0.021 (2) A ˚ from the mean plane. The crystal structure is stabilized by intermolecular C—H....N interactions, leading to the formation of a layer-like structure, which extends along the a axis |
| URI: | http://dyuthi.cusat.ac.in/jspui/handle/dyuthi/1642 |
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| Acta E Digna.pdf | (313.7Kb) |
| Abstract: | A novel bisazomethine Schiff base was synthesised by the condensation of 3-hydroxyquinoxaline-2- carboxaldehyde and 2,3-diaminomaleonitrile. 1H NMR, 13C NMR, HPLC and FT-IR studies revealed that the compound exists in two major tautomeric forms. The Schiff base exhibits positive absorption and fluorescent solvatochromism and displays dual fluorescence with large stoke shifts. Cyclic voltammetric analysis of the compound in 1:1 methanol–THF was influenced by scan rate. Thermal analysis of the compound was undertaken using TG–DTA and DSC |
| URI: | http://dyuthi.cusat.ac.in/purl/1645 |
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| dyes.pdf | (678.4Kb) |
| Abstract: | The mononuclear cobalt(II) complex [CoL2] H2O (where HL is quinoxaline-2-carboxalidine- 2-amino-5-methylphenol) has been prepared and characterized by elemental analysis, conductivity measurement, IR, UV-Vis spectroscopy, TG-DTA, and X-ray structure determination. The crystallographic study shows that cobalt(II) is distorted octahedral with each tridentate NNO Schiff base in a cis arrangement. The crystal exhibits a 2-D polymeric structure parallel to [010] plane, formed by O-H...N and O-H... O intermolecular hydrogen bonds and pye stacking interactions, as a racemic mixture of optical enantiomers. The ligand is a Schiff base derived from quinoxaline-2-carboxaldehyde |
| URI: | http://dyuthi.cusat.ac.in/jspui/handle/dyuthi/1638 |
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| 665515_758077589_915864698.pdf | (576.1Kb) |
| Abstract: | An efficient one-pot synthesis of two new heterocyclic perimidines 4-(2,3-dihydro-1H-perimidin-2-yl)-2-methoxyphenol and 2-(quinoxalin-2-yl)-2,3-dihydro-1H-perimidine in good yields is presented. This methodology provides a simple, straightforward synthetic route to these interesting classes of heterocycles. Crystal structure, solvatochromism and antibacterial activity of these organic compounds are discussed. |
| URI: | http://dyuthi.cusat.ac.in/purl/1640 |
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| tet let varsha.pdf | (437.1Kb) |
| Abstract: | The Schiff base compounds N,N0-bis[(E)-quinoxalin-2-ylmethylidene] propane-1,3-diamine, C21H18N6, (I), and N,N0-bis[(E)- quinoxalin-2-ylmethylidene]butane-1,4-diamine, C22H20N6, (II), crystallize in the monoclinic crystal system. These molecules have crystallographically imposed symmetry. Compound (I) is located on a crystallographic twofold axis and (II) is located on an inversion centre. The molecular conformations of these crystal structures are stabilized by aromatic pye stacking interactions. |
| URI: | http://dyuthi.cusat.ac.in/jspui/handle/dyuthi/1641 |
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| Acta Cryst. (2009). C65, o612_o614.pdf | (390.4Kb) |
| Abstract: | The asymmetric unit of the title compound, C11H8N4, contains two independent molecules. In the crystal structure, intermolecular N—H.....N hydrogen bonds link molecules into ribbons extended in the [100] direction |
| URI: | http://dyuthi.cusat.ac.in/purl/1643 |
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| acta e varsha.pdf | (213.4Kb) |
Now showing items 1-7 of 7
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