Coordination compounds of copper(II), nickel(II), and cobalt(II) with β-thiosemicarbazones of isatin and N-methylisatin
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SAMUSI, Nina, TSAPKOV, Victor I., GULYA, Aurelian. Coordination compounds of copper(II), nickel(II), and cobalt(II) with β-thiosemicarbazones of isatin and N-methylisatin. In: Russian Journal of General Chemistry, 2004, vol. 74, pp. 1428-1432. ISSN 1070-3632. DOI: https://doi.org/10.1007/s11176-005-0026-3
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Russian Journal of General Chemistry
Volumul 74 / 2004 / ISSN 1070-3632 /ISSNe 1608-3350

Coordination compounds of copper(II), nickel(II), and cobalt(II) with β-thiosemicarbazones of isatin and N-methylisatin

DOI:https://doi.org/10.1007/s11176-005-0026-3

Pag. 1428-1432

Samusi Nina, Tsapkov Victor I., Gulya Aurelian
 
Moldova State University
 
 
Disponibil în IBN: 21 septembrie 2023


Rezumat

Isatin thiosemicarbazone (HL) reacts in aquoeus-ethanolic medium with copper(II) chloride and bromide (pH 7-7.5, ethanolic KOH) to give coordination compounds CuLX·nH2O (X = Cl, Br; n = 3, 4). In the presence of amines (A = C5H5N, 3-CH3C54N, and 4-CH3C5H4N), complexes CuALX·2H2O and CuA2LX·H2O (X = Cl, Br) are formed. With nickel(II) or cobalt(II) chlorides, thiosemicarbazone HL, and pyridine (1:1:3) as starting compounds, compounds MPy 2LCl·H2O (M = Ni, Co) are isolated. Under similar conditions, N-methylisatin β-thiosemicarbazone (HL') reacts with chlorides of the above-noted metals in the presence of pyridine to give complexes MPy 2L'Cl·H2O (M = Cu, Ni, Co). All the complexes are monomeric and have a pseudooctahedral structure of the coordination unit. Thiosemicarbazones HL and HL1 in these complexes behave as tridentate monodeprotonated O,N,S-ligands. Thermolysis of these substances passes through the stages of dehydration (60-90°C), deaquation (135-140°C) or deamination (160-215°C), and complete thermal decomposition (560-670°C). 

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<cfAbstr cfLangCode='EN' cfTrans='o'><p>Isatin thiosemicarbazone (HL) reacts in aquoeus-ethanolic medium with copper(II) chloride and bromide (pH 7-7.5, ethanolic KOH) to give coordination compounds CuLX&middot;nH<sub>2</sub>O (X = Cl, Br; n = 3, 4). In the presence of amines (A = C<sub>5</sub>H<sub>5</sub>N, 3-CH<sub>3</sub>C<sub>5</sub>H&nbsp;<sub>4</sub>N, and 4-CH<sub>3</sub>C<sub>5</sub>H<sub>4</sub>N), complexes CuALX&middot;2H<sub>2</sub>O and CuA<sub>2</sub>LX&middot;H<sub>2</sub>O (X = Cl, Br) are formed. With nickel(II) or cobalt(II) chlorides, thiosemicarbazone HL, and pyridine (1:1:3) as starting compounds, compounds MPy&nbsp;<sub>2</sub>LCl&middot;H<sub>2</sub>O (M = Ni, Co) are isolated. Under similar conditions, N-methylisatin &beta;-thiosemicarbazone (HL&#39;) reacts with chlorides of the above-noted metals in the presence of pyridine to give complexes MPy&nbsp;<sub>2</sub>L&#39;Cl&middot;H<sub>2</sub>O (M = Cu, Ni, Co). All the complexes are monomeric and have a pseudooctahedral structure of the coordination unit. Thiosemicarbazones HL and HL<sup>1</sup>&nbsp;in these complexes behave as tridentate monodeprotonated O,N,S-ligands. Thermolysis of these substances passes through the stages of dehydration (60-90&deg;C), deaquation (135-140&deg;C) or deamination (160-215&deg;C), and complete thermal decomposition (560-670&deg;C).&nbsp;</p></cfAbstr>
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