2018
DOI: 10.14233/ajchem.2019.21475
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Biological Applications of Co(II) and Ni(II) Complexes of Semicarbazones and Thiosemicarbazones

Abstract: Due to their borad profiles of biological activities, transition metal complexes containing semicarbazones and thiosemicarbazones become largely appealing. This mini review focused on the recent developments in last 5 years on the biological applications of Co(II) and Ni(II) complexes of semicarbazones and thiosemicarbazones.

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Cited by 12 publications
(3 citation statements)
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“…[2] Thiosemicarbazones (NH 2 À NHÀ CSNH 2 ) are the chelating ligands that coordinate with transition metal ions to form complexes and have drawn a lot of attention owing to diverse pharmacological and physiological features. [3] These thiosemicarbazone are usually synthesized via condensation of thiosemicarbazide and carbonyl (aldehyde/ketone) compounds. [4] As thione-thiol tautomers, thiosemicarbazides can coordinate with metal ions neutrally or anionically, depending on whether a proton is lost from thiol-sulfur (SH) or thio-amide nitrogen (NH).…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[2] Thiosemicarbazones (NH 2 À NHÀ CSNH 2 ) are the chelating ligands that coordinate with transition metal ions to form complexes and have drawn a lot of attention owing to diverse pharmacological and physiological features. [3] These thiosemicarbazone are usually synthesized via condensation of thiosemicarbazide and carbonyl (aldehyde/ketone) compounds. [4] As thione-thiol tautomers, thiosemicarbazides can coordinate with metal ions neutrally or anionically, depending on whether a proton is lost from thiol-sulfur (SH) or thio-amide nitrogen (NH).…”
Section: Introductionmentioning
confidence: 99%
“…As a result, a number of such novel compounds are reported into this field each year [2] . Thiosemicarbazones (NH 2 −NH−CSNH 2 ) are the chelating ligands that coordinate with transition metal ions to form complexes and have drawn a lot of attention owing to diverse pharmacological and physiological features [3] . These thiosemicarbazone are usually synthesized via condensation of thiosemicarbazide and carbonyl (aldehyde/ketone) compounds [4] .…”
Section: Introductionmentioning
confidence: 99%
“…Over many years, thiosemicarbazide has been the strong intermediate for developing various novel biomaterials and, therefore, widely utilized in pharmaceutical and medicinal industries. [2,3] The significant biological action [4][5][6][7][8] provided the driving force for exploring the coordination chemistry of these potent ligands. These ligands were also commercially used as analytic reagents, [9,10] catalyst, [11][12][13] molecular-magnetic material, [14] spin-crossover materials, [15] chemosensor to detect Hg 2 + ions, [16] fluoride anions and inorganic cations.…”
Section: Introductionmentioning
confidence: 99%