Thiosemicarbazones metal complexes

Metal complexes of ligands containing a sulfur donor in conjunction with nitrogen, oxygen or a second sulfur have been reviewed in the past [11-13]. For example, reviews of the coordination compounds of dithiophosphates [14], dithiocarbamates [15, 16], dithiolates [17], dithiodiketonates [18], and xanthates [16] have appeared. The analytical aspects [19] and the spectral and structural information of transition metal complexes of thiosemicarbazones [20, 21] have been reviewed previously. Recent developments in the structural nature of metal complexes of 2-heterocyclic thiosemicarbazones and S-alkyldithiocarbazates, depicted below, are correlated to their biological activities. 

The copper(II) complexes of 3-ethoxy-2-oxobutyraldehyde bis(thiosemicarbazone) and related compounds are active in vivo agents [151, 158, 159]. The metal complexes of 2-heterocyclic thiosemicarbazones were evaluated for their cytotoxicities [160, 161]. Further studies have revealed that these ligand s iron and copper complexes are effective inhibitors of DNA synthesis at much lower concentrations than the free thiosemicarbazones without apparent cytotoxicity [127]. Although the iron(III) complex of 2-isoformylquinoline thiosemicarbaz-one, 21, is considerably more active than free 21, the copper(II) complex is only moderately more active [127]. 

One of the few crystal structures solved for a metal complex of a heterocyclic thiosemicarbazone is bis(l-formylisoquinoline thiosemicarbazone) nickel(II) monohydrate, [Ni(21-H)2] (Fig. 5) [208]. The nickel(II) center was found to be NNS coordinated by two approximately planar thiosemicarbazone ligands. 

Although 4-methyl-5-amino-1-formylisoquinoline thiosemicarbazone, 22, also forms [Ni(22)Cl2] with chemical properties similar to [Ni(21)Cl2], it, along with other metal complexes of 22, showed no activity against P388 lymphocytic leukemia test system in mice [202]. 

The coordination shell comprises three fac-S and three fac-N-donor atoms in [Fe(6mp)3] [FeClJCl, where 6mp = 6-thiopurine, (189). Both iron(II) and iron(III) complexes are included in a review of transition metal complexes of thiosemicarbazones. " 5,5 -Dimethyl-l,2,3-cyclohex-anetrione-l,2-dioxime-3-thiosemi-carbazone, dcdt (190), acts as an A, A, 5 -donor to Fe +, giving a bis-ligand complex (contrast [Fe(7V,7V -dcdt)3] with Fe " "). The Schiff bases from pyridine 2-carboxaldehyde and thiosemicarbazide or 4-phenyl thiosemicarbazide also act as A, VV, 5 -donors, both to Fe " " and to Fe " ". The antibacterial activity of these complexes was assessed, in... 

The reactions of silver(I) with 1,5-diphenyl thiocarbazone (56 dithizone = HaDz) by comparison to thiosemicarbazones have been thoroughly investigated.442,444 Dithizone has for many years been used as a colorimetric reagent for trace metal ions. Its metal complexes are of two types, the so-called primary and secondary dithizonates. Primary dithizonates are generally formed at low pHs where the ligand becomes mono depronated (pA = 4.5) but retains the NH proton. Secondary dithizonates are formed in the presence of an excess of metal and/or at higher pH values where the ligand becomes fully deprotonated. Since it has been estimated that for free dithizone pK2 > 15, the second proton obviously becomes labilized in the presence of metal ions. 

Murugkar, A. Padhye, S. Guha-Roy, S. Wagh, U. Metal complexes of Taxol precursor 1. Synthesis, characterization and antitumor activity of the copper complex of 10-deacetylbaccatin thiosemicarbazone. Inorg. Chem. Commun., 1999, 2 545-548. 

A variety of metal complexes of isatin-3-thiosemicarbazones 279.386-390 and isatin-3-semicarbazones have been prepared. 

Tridentate thiosemicarbazones having a N2S donor set are known80 as well as the crystal structure of the N2S free SB 2-pyridineformamide 3-piperidylthiosemicarbazone.81 Metal complexes of thiosemicarbazones have been reviewed and numerous examples of sulfur-containing SB ligands may be found in Casas et al.29... 

Li, Y., Yang, Z-Y., Wu, J-C. (2010). Synthesis, crystal structures, biological activities and fluorescence studies oftransition metal complexes with 3-carbaldehyde chromone thiosemicarbazone. Europ.. Med. Chem., 45, pp. 5692-5701, ISSN 0223-5234... 

The possibility that certain metal complexes of a-(A()-heterocyclic carbox-aldehyde thiosemicarbazones may be cytotoxic to tumour cells has been examined [58,60-62]. 

Chelating agents may manifest their antiviral activity by metal sequestration and, as with bacteria and parasites, the natural differences between the host and invading cells may be exploited. Chelating agents with antiviral activity include the thiosemicarbazones, 1,10-phenanthrolines and phosphonoacetates. The latter compounds may act by zinc chelation. Metal complexes with antiviral action are platinum and palladium amines, as well as the antibacterial silver and mercury species. 

The synthesis of iron, cobalt and nickel complexes of 2-fomiylpyridine thiosemicarbazone has been reported [59]. The a-(AO-heterocyclic carboxaldehyde thiosemicarbazones strongly complex transition metals through their N -N -S ... 

Iron(II) complexes are often included in studies when complexes are prepared from a large number of different metal ions. 2-formylpyridine thiosemicarbazone, 5, forms brown [Fe(5)2A2] (A = Cl, Br) when prepared in ethanol and [Fe(5-H)2] from aqueous alcohol solution [156], All of these complexes are diamagnetic. The resonance Raman and infrared spectra of [Fe(5-H)2] were examined in detail [130] and coordination occurs via the pyridyl nitrogen, azomethine nitrogen and thiol sulfur. There is appreciable d-d sulfur-to-iron(II) Jt-bonding. Solution studies of iron(II) complexes of some 5-substituted-2-formylpyridine thiosemicarbazones have been reported [157], but no solids... 

Two copper(II) complexes of 2-acetylpyridine thiosemicarbazone, 8, were included in a study of complexes of 2-formylpyridine thiosemicarbazone [169]. [Cu(8-H)OAc] has a magnetic moment consistent with a monomeric copperfll) center and both it and [Cu(8)Cl2] have d,2-y2 ground state ESR spectra (Table 2). A d-d envelope and a magnetic moment of 1.68 B.M. have led others [178] to propose a distorted tetrahedral environment with metal-metal interaction for the brown complex, [Cu(8)Cl2]. 

Methyl-5-amino-l-formylisoquinoline thiosemicarbazone, 22, also yields cobalt(II) complexes from unheated methanol solution [202]. However, due to this ligand s added steric requirements, a complex, [Co(22)Cl2], with one ligand per metal ion center is formed. This brown solid has a magnetic moment of 4.42 B.M., is a non-electrolyte, has coordination of a neutral NNS ligand, and the electronic spectrum indicates approximate trigonal bipyramidal stereochemistry. 

---