Abstract

The title compound, C23H18N2O2·0.5H2O, a derivative of the biologically active compound curcumin, crystallizes with two organic mol­ecules and a solvent water mol­ecule in the asymmetric unit. Each of the two independent mol­ecules is close to being planar (the dihedral angles between the indole ring systems are approximately 9 and 12°) and each exists in the keto–enol form. There is an intra­molecular O—H⋯O hydrogen bond between the keto and enol groups. In the crystal, the components interact by way of N—H⋯N, N—H⋯O and O—H⋯O hydrogen bonds.

Highlights

  • The title compound, C23H18N2O20.5H2O, a derivative of the biologically active compound curcumin, crystallizes with two organic molecules and a solvent water molecule in the asymmetric unit

  • Each of the two independent molecules is close to being planar and each exists in the keto–enol form

  • The title compound, (I) (Fig. 1), is new to this class of compounds and crystallizes with two molecules and a solvent water molecule in the asymmetric unit.The two independent molecules are close to being planar as indicated by the torsion angles along the chains with molecule 2 being less planar than molecule 1

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Summary

Structure Reports

Absolute structure: the absolute structure could not be determined with certainty. H-atom parameters constrained a School of Chemistry and Chemical Engineering, Henan University of Technology, Zhengzhou 450001, People’s Republic of China, and bDepartment of Chemistry, Tulane University, New Orleans, LA 70118, USA. R factor = 0.033; wR factor = 0.084; data-to-parameter ratio = 10.2. The title compound, C23H18N2O20.5H2O, a derivative of the biologically active compound curcumin, crystallizes with two organic molecules and a solvent water molecule in the asymmetric unit. Each of the two independent molecules is close to being planar (the dihedral angles between the indole ring systems are approximately 9 and 12 ) and each exists in the keto–enol form. There is an intramolecular O—H O hydrogen bond between the keto and enol groups. The components interact by way of N—H N, N—.

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This work was supported by the Research Foundation of
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