Synthesis and Characterization of Ortho-Halogen-Substituted Mono- and Bisthiocarbohydrazones: Structural Comparison

Six ortho-substituted halogen derivatives (F, Cl, Br) of mono- and analog bisthiocarbohydrazones were synthesized and fully characterized. Structural characterization was performed through elemental analysis and NMR, FT-IR and UV-Vis spectroscopy. Also, all compounds were successfully isolated in the form of single crystals, and X-ray analysis was applied. Through the comparative structural analysis, similarities and differences of the mono- and bisubstituted derivatives were discussed on the molecular level, but also in terms of crystal packing. Special focus was on the assessment of the influence of the additional condensation and intramolecular interactions on molecular geometry and supramolecular organization. In addition, thermal properties of all compounds were analyzed, and for monosubstituted derivatives, ionization constants of the terminal amino group were determined.

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Journal
Organics
Published
2026-10-09
DOI
https://doi.org/10.3390/org7040042
Primary Topic
Crystal structures of chemical compounds
Type
article
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article

Synthesis and Characterization of Ortho-Halogen-Substituted Mono- and Bisthiocarbohydrazones: Structural Comparison

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article

Synthesis and Characterization of Ortho-Halogen-Substituted Mono- and Bisthiocarbohydrazones: Structural Comparison

Borko Matijević, Berta Barta Holló, Olivera Marković, Milica G. Bogdanović, Mirjana M. Radanović, Marko V. Rodić, Gorana Mrđan
article en

Abstract

Six ortho-substituted halogen derivatives (F, Cl, Br) of mono- and analog bisthiocarbohydrazones were synthesized and fully characterized. Structural characterization was performed through elemental analysis and NMR, FT-IR and UV-Vis spectroscopy. Also, all compounds were successfully isolated in the form of single crystals, and X-ray analysis was applied. Through the comparative structural analysis, similarities and differences of the mono- and bisubstituted derivatives were discussed on the molecular level, but also in terms of crystal packing. Special focus was on the assessment of the influence of the additional condensation and intramolecular interactions on molecular geometry and supramolecular organization. In addition, thermal properties of all compounds were analyzed, and for monosubstituted derivatives, ionization constants of the terminal amino group were determined.

OrganicsVol. 7(4)
University of Novi Sad (RS), University of Belgrade (RS), Institute of Chemistry, Technology and Metallurgy
Openalex Percentile: Top 28%
Crystal structures of chemical compounds
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