
Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry p. 979 - 995 (2000)
Update date:2022-08-04
Topics:
Kandil, Samir S.
El-Brollosy, Nasser R.
El-Dissouky, Ali
Manganese(II), nickel(II) and copper(II) complexes of 4-(2,6-dichlorobenzylidene-amino)-3-mercapto-6-methyl-1,2,4-triazin-5(4H)-one (HL1) and 4-(cinnamylidene-amino)-3-mereapto-6-methyl-1,2,4-triazin-5(4H)-one (HL2) have been synthesized and characterized. The IR spectra indicate that both HL1 and HL2 act as neutral or monobasic bidentate ligands, coordinating to metal ions via azomethine-N and either carbonyl-O or (thiolo or thiono)-S, depending on the metal ion. The magnetic and spectroscopic data suggest a distorted-octahedral geometry for the Ni(II) complexes, a square-planar geometry for [L1CuCl(H2O)], a dimeric distorted octahedral geometry for both [(L2)2Cu(H2O)]2 and [(HL)Mn(SO4)(H2O)2]2. Such dimeric structures have been revealed by the subnormally low μeft values for the Mn(II) complexes, due to antiferromagnetic coupling between the two Mn(II) centers, and the diamagnetism of [(L2)2Cu(H2O)]2 is due to a quenching mechanism. ESR parameters support the structures of the Mn(II) and Cu(II) complexes and that the two azomethine nitrogens are coordinated to the Cu(II) ion in the [(L2)2Cu(H2O)]2 complex. DTA studies of the maganese(II) and copper(II) complexes are also reported.
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