2. Articole

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    Coordination compounds of copper(II) with benzoylhydrazones of substituted salicylaldehydes [Articol]
    (2003) Samusi, Nina; Țapcov, Victor; Kerner, A.
    Benzoylhydrazones of 5-nitro- (H2L1), 3-nitro- (H2L2), 5-chloro- (H2L3), 5-bromo- (H2L4), and 3,5-dibromosalicylaldehydes (H 2L5) react in ethanol with copper acetate to form complexes CuL1-5. In the presence of amines (A = C5H 5N, 3-CH3C5H4N), the above reactions give complexes CuL1-5A·nH2O (n = 0, 1). When cuprous bromide or nitrate and benzoylhydrazone H2L3 were used as starting materials, complexes Cu(HL3)X (X = Br-, NO3-) were isolated. The resulting complexes all are polynuclear structures in which azomethines H2L1-5 behave as tridentate O,N,O-ligands. Thermolysis of the complexes involves the stages of dehydration (70-90°C), deaquation (120-150°C) or deamination (150-180°C), and complete thermal decomposition (350-500°C).
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    Coordination compounds of copper(II), nickel(II), and cobalt(II) with β-thiosemicarbazones of isatin and N-methylisatin [Articol]
    (2004) Samusi, Nina; Țapcov, Victor; Gulea, Aurelian
    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-CH3C5H 4N, 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).