Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 1150, Issue -, Pages 44-54Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molstruc.2017.08.062
Keywords
Isoxazole; Thiosemicarbazone; Schiff base; DNA; Albumin; Hirshfeld surface
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Funding
- Brazilian funding agency CNPq [472530/2012-7]
- Brazilian funding agency FAPEMIG [APQ-01253-15]
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Six new 3;5-isoxazole thiosemicarbazone derivatives (ITCs) (HL1 - HL6) were synthesized and characterized using microanalysis, spectroscopic methods and for HL2, HL3, HL5 and HL6a by a single crystal Xray diffraction. The combined analyses, utilizing NMR and X-ray techniques, showed that the compounds presented an E conformation both in solution and solid state. The intermolecular N3-H3N center dot center dot center dot S1 hydrogen bonds, between the thiosemicarbazone groups, resulted in rings for all crystals. For HL2 and HL5, one medium strength (N4-H4N center dot center dot center dot S1) and one weak (C8-H8 center dot center dot center dot N1) intermolecular hydrogen bond was also observed. HL3 presented a pi(ar)-pi(ar) stacking interaction and HL6a was stabilized by three hydrogen bonds involving DMSO oxygen. The interconnections in the crystal structures were analyzed using Hirshfeld surfaces. The interaction studies, using fluorescence and absorbance spectroscopy, showed that the ITCs interacted with DNA and human serum albumin (HSA). (C) 2017 Elsevier B.V. All rights reserved.
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