Abstract

In the mol-ecule of the title compound, C16H20N2O6S2, the mid-point of the C-C bond of the central ethane moiety is located on a twofold rotation axis. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds into supra-molecular chains propagating along the [101] direction. Hirshfeld surface analysis and two-dimensional fingerprint plots indicate that the most important contributions to the crystal packing are from H⋯H (43.1%), O⋯H/H⋯O (40.9%), C⋯H/H⋯C (8.8%) and C⋯C (5.5%) inter-actions.

Highlights

  • In the molecule of the title compound, C16H20N2O6S2, the mid-point of the C—C bond of the central ethane moiety is located on a twofold rotation axis

  • Molecules are linked by N—HÁ Á ÁO hydrogen bonds into supramolecular chains propagating along the [101] direction

  • Hirshfeld surface analysis and twodimensional fingerprint plots indicate that the most important contributions to the crystal packing are from HÁ Á ÁH (43.1%), OÁ Á ÁH/HÁ Á ÁO (40.9%), CÁ Á ÁH/ HÁ Á ÁC (8.8%) and CÁ Á ÁC (5.5%) interactions

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Summary

Chemical context

Sulfonamides are synthetic molecules which include the SO2– NH group and are called sulfa drugs. These effective drug molecules have an important role in the medical field, including as promising chemotherapeutic agents, and have been used in the treatment of many bacterial infections due to their physical, chemical and biological properties (Mahmood et al, 2016; Ghorab et al, 2018). N,N0-ditosylalkane diamine is a disulfonamide synthesized by the tosylation of diamine, and this synthetic molecule has antibacterial properties (Alyar et al, 2011) and has been used in many organic synthesis reactions (Rong et al, 1998). Symmetry codes: (i) Àx þ 12; Ày þ 12; Àz; (ii) x þ 12; y þ 12; z

Structural commentary
Supramolecular features
Database survey
Hirshfeld surface analysis
82 Meral et al C16H20N2O6S2
Refinement
Findings
85 Meral et al C16H20N2O6S2 supporting information supporting information
Full Text
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