Academic literature on the topic 'Cyclohexanone Thiosemicarbazone'

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Journal articles on the topic "Cyclohexanone Thiosemicarbazone"

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Sadavarte, Prajakta Shamrao, Bhaskar Hari Zaware та Sushama Jayawant Takate. "Kinetics of Thiazole Formation Using α-Halo Ketones and Thioamides". Oriental Journal Of Chemistry 38, № 4 (2022): 1031–36. http://dx.doi.org/10.13005/ojc/380427.

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The current approach involves the kinetic investigation of Thiobenzamide (TB) and cyclohexanone thiosemicarbazone (CTSC) in solution with 3-chloroacetylacetone(3-CAA). The study revealed a second-order rate constant with respect to both reactants, thioamide and an α-halo carbonyl compound. The energy of activation (Ea) was found to be Ea 48.8176 kJ/mol/K for thiobenzamide and 33.08692157 kJ/mol/K for Cyclohexanone thiosemicarbazone. The salt effect study showed the formation of ionic species during the reaction. The reactions were studied with respect to changes in dielectric constant using solvent systems like water-ethanol and water-isopropanol.
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Moskvina, Viktoria, Olexander Turov, Tetyana Shokol, and Volodymyr Khilya. "Synthesis and NMR spectroscopy investigations of functionalized spiropyranochromenediones and their spirothiadiazole derivatives." Ukrainica Bioorganica Acta 16, no. 2 (2021): 18–22. http://dx.doi.org/10.15407/bioorganica2021.02.018.

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This investigation focuses on the synthesis of spiropyranoneoflavones and the modification of obtained compounds at the exocyclic oxygen atom. Kabbe cyclization of 6-acetyl-7‑hydroxy-8-methyl-4-phenyl-2H-chromene-2-one with cyclohexanone or cyclopentanone in the presence of pyrrolidine provided 10-methyl-4-phenyl-2H-spiro[cyclohexane(cyclopentane)-1’,8-pyrano[3,2-g]chromene]-2,6(7H)-diones. Their new functionalized derivatives with thiosemicarbazide residues were synthesized. Acetylation of obtained thiosemicarbazones with acetic anhydride proceeded via cyclization of thiosemicarbazide fragment into 1,3,4-thiadiazole ring to give corresponding N-[3'-acetyl-10-methyl-8-oxo-6-phenyl-3'H,8H-dispiro[cyclohexane-1,2’-pyrano[3,2-g]chromene-4,2'-[1,3,4]thiadiazol]-5'-yl]acetamide and N-[3'-acetyl-10-methyl-8-oxo-6-phenyl-3'H,8H-dispiro[cyclopentane-1,2’-pyrano[3,2-g]chromene-4,2'-[1,3,4]thiadiazol]-5'-yl]acetamide. The structure of the obtained compounds was confirmed by NMR spectroscopy
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Ali, Al-Ameen Bariz Omar. "Synthesis, Characterization and Kinetic Study of Monomeric Complexes of Cyclohexane-1, 2- bis (Thiosemicarbazone) with Cobalt (II), Nickel (II) and Copper (II)." Al-Mustansiriyah Journal of Science 28, no. 2 (2018): 48. http://dx.doi.org/10.23851/mjs.v28i2.499.

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Cyclohexane-1,2-bis(thiosemicarbazone) (CHTSC) was synthesized via the condensation reaction of cyclohexane-1,2-dione and thiosemicarbazide. Series of metal complexes of the prepared lig-and, of general formula [M(CHTSC)(NO3)2], were reported. The prepared coordination complex-es were characterized and their structures elucidated using different techniques. These showed that all complexes are octahedral geometries. The kinetics of the formation of these complexes have been investigated using stopped-flow spectrophotometry. These studies revealed that the reactions are completed on the second’s timescale with 1st-order dependence (either on the con-centration of metal salt or on the concentration of CHTSC).
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Yousif, Enaam Ismail, Nihad Kadhum Hasan, and Mohamad J. Al Jeboori. "New Metal Complexes of Thiosemicarbazone Mannich base Ligand; Synthesis, Structural Characterisation and Biological Activity." Pakistan Journal of Medical and Health Sciences 16, no. 6 (2022): 565–70. http://dx.doi.org/10.53350/pjmhs22166565.

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The synthesis of a new tridentate Schiff-base thiosemicarbazone ligand (HL) that derived from the reaction of ((R)-2-((4-(dimethylamino)phenyl)((2-nitrophenyl)amino)methyl)-5,5-di methyl- cyclohexane-1,3-dione with thiosemicarbazide is reported. The reaction of the title ligand(E)-2-((R)-2-((R)-(4-(dimethylamino)phenyl)((2-nitrophenyl)amino)methyl)-5,5-dimethyl-3-oxocyclohexylidene)hydrazine-1-carbothioamide with selected metal ions of Co(II), Ni(II), Cu(II), Zn(II) and Cd(II) gave the title monomeric complexes. Analytical and spectroscopic techniques were used, as required, to characterise the prepared compounds. These include; elemental microanalysis, 1H, 13C-NMR and mass spectra, FT-IR and electronic spectra, magnetic susceptibility and conductance. These analyses revealed the formation of monomeric complexes of octahedral arrangement about Co(II); Cu(II) and square planar and tetrahedral geometry with the Ni(II) and Zn(II); Cd(II)) ions, respectively. Thermal stability (TGA-DSC) of HL and selected complexes were also explored. The antimicrobial activity of the title compounds (ligand and complexes) towards several microorganism (bacteria and fungi species) were examined. The collected data revealed the antimicrobial activity of the ligand was enhanced upon complex formation. Keywords: Thiosemicarbazone ligand, Metal complexes, Structural investigation, Thermal stability, Antimicrobial activity.
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Sigmundová, Ivica, and Mária Mečiarová. "Synthesis of New 2-Hydrazono-4-oxo-5-thiazolidineacetic Acids and Their Alkylamides." Collection of Czechoslovak Chemical Communications 62, no. 1 (1997): 124–29. http://dx.doi.org/10.1135/cccc19970124.

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The direct two step synthesis of three new 2-hydrazono-4-oxo-5-thiazolidineacetic acids from thiosemicarbazide, the appropriate ketones (acetophenone, cyclopentanone, cyclohexanone) and maleic anhydride is described. The prepared acids were transformed, via their mixed anhydrides with ethyl carbonate, into their alkylamides in a one-pot procedure.
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Sulekh, Chandra, Kumar Singh Chandan, and Agarwal Himanshu. "Polymeric membrane ion-selective electrode for copper(II) ions based on CuII-cyclohexaneone thiosemicarbazone complex." Journal of Indian Chemical Society Vol. 84, Mar 2007 (2007): 291–92. https://doi.org/10.5281/zenodo.5816562.

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Department of Chemistry, Zakir Husain College, University of Delhi, J.L. Nehru Marg, New Delhi-110 002, India <em>E-mail </em>: schandra_OO@yahoo.com Fax : 91-11-234276530 <em>Manuscript received 11 August 2006, revised 22 January 2007, accepted 22 January 2007</em> A PVC-based membrane of copper(II)-cyclohexaneone thiosemicarbazone complex shows a Nernstain poteniometric response (with slope of 29.2 mV/decade) for copper(II) ions over a wide concentration range (1 x 10<sup>-</sup>1 to 1 x 10<sup>-9</sup> <em>M</em>). The potential of the electrode is independent of pH in the range 2.0-7.0. It has a fast response of about 15 s and was used for a period of 2 months with good reproducibility.
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Oliveira, Adriano Bof de, Johannes Beck, Jörg Daniels, Renan Lira de Farias, and Adelino Vieira de Godoy Netto. "Crystal structure of (E)-2-[(2S,5R)-2-isopropyl-5-methylcyclohexylidene]hydrazine-1-carbothioamide." Acta Crystallographica Section E Structure Reports Online 70, no. 9 (2014): o903—o904. http://dx.doi.org/10.1107/s1600536814015980.

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The title compound, C11H21N3S, consists of a menthone moiety attached to an extended thiosemicarbazone group with the N—N—C—N torsion angle being 11.92 (16)°. The cyclohexane ring has a chair conformation and the conformation about the C=N bond isE. In the crystal, molecules are linkedviapairs of N—H...S hydrogen bonds, forming chains along theaaxis. The absolute structure could be assigned with reference to the starting material,i.e.enantiopure (−)-menthone [Flack parameter = 0.05 (5)].
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Lobana, T. S., Rekha, R. J. Butcher, T. W. Failes, and P. Turner. "Crystal structures of organomercury(II) derivatives of cyclohexanone and benzaldehyde thiosemicarbazones." Journal of Coordination Chemistry 58, no. 15 (2005): 1369–75. http://dx.doi.org/10.1080/00958970500241415.

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Ambewadikar, Rahul Gautam, Rajesh Deshmukh, and Mahesh G. Shioorkar. "Synthesis, Characterization, and Antimicrobial Activity of Novel Pyrazolylthiazole Derivatives from Curcumin Analogues." International Journal of Advance and Applied Research 11, no. 3 (2024): 367–70. https://doi.org/10.5281/zenodo.14753419.

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<strong>Abstract</strong> Curcumin and its derivatives have garnered significant attention in medicinal chemistry due to their versatile therapeutic potential, including antimicrobial, anti-inflammatory, and anticancer properties. This study focuses on the synthesis, characterization, and antimicrobial activity of pyrazolylthiazole derivatives derived from curcumin analogues. Curcumin, demethoxycurcumin, and bis-demethoxycurcumin were isolated from natural sources and used as precursors for the synthesis of pyrazolylthiazole derivatives through reactions involving anisaldehyde, cyclohexanone, and thiosemicarbazide under optimized conditions. The synthesized compounds were characterized using spectroscopic techniques such as IR, NMR, and mass spectrometry to confirm their structures. In vitro antimicrobial evaluation against bacterial and fungal strains revealed significant activity, with some derivatives demonstrating superior efficacy compared to standard drugs. These findings highlight the potential of pyrazolylthiazole derivatives as promising candidates for developing novel antimicrobial agents and contribute to the growing interest in heterocyclic compounds for therapeutic applications.
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Pandey, V. K., та N. Raj. "Synthesis of α-methyl-benzamido-α′-substituted styryl cyclohexanone thiosemicarbazones as potential antifertility agents". Pharmacological Research Communications 18, № 10 (1986): 923–33. http://dx.doi.org/10.1016/0031-6989(86)90096-2.

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Book chapters on the topic "Cyclohexanone Thiosemicarbazone"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed valence copper(II)–copper(I) complex with cyclohexanone thiosemicarbazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_382.

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