in present studies the synthesis, characterization and biological properties ofoxovanadium(iv) coordination compounds of 4[n-(4′-ethylbenzalidene)amino] antipyrinethiosemicarbazone (ebaapts) and 4[n-(2′,4′-dimethylbenzalidene)amino] antipyrinethiosemicarbazone (dmbaapts) with the general composition vox2l (x = c1-, br-, i-, no3-or ncs-) and vo(cio4)2(l)h2o (l = ebaapts or dmbaapts) are describe...

the in-situ method of synthesis has been used to isolate oxovanadium(iv) complexes with ligands derived by reaction of benzil with amino acids such as glycine, alanine, serine, cysteine and valine, where template effect of vo +2 cation appears to play an important role. the complexes are characterised by elemental analysis, magnetic moment measurements and spectral (infrared, electronic and ele...

In a systematic effort to identify a potent anticancer agent, we synthesized 15 oxovanadium(IV) complexes and examined their cytotoxic activity against 14 different human cancer cell lines. The oxovanadium compounds included mono and bis ancillary ligands of 1,10-phenanthroline (phen) [VO(phen), VO(phen)2, VO(Me2-phen), VO (Me2-phen)2, VO(Cl-phen), VO(Cl-phen)2, VO(NO2-phen), VO(NO2-phen)2], 2,...

Oxovanadium(IV) complexes of the type [VO(mac)]SO4 , (where mac = tetraaza macrocyclic ligands derived by condensation of furil with 1,4-diaminobenzene or 3,4-diaminopyridine and their reaction with βdiketones) have been prepared using vanadyl ion as kinetic template. Tentative structures of the complexes have been proposed on the basis of elemental analysis, infrared, e.s.r. and electronic dat...

The oxovanadium(IV) complexes LVO and L'VO (L = dianion of 5,14-dihydro-6,8,15.17tetramethyldibenzo[b.i][l,4.8,ll]tetraazacyclotetradecine. H2L. and L' = dianion of 5.14-dihydro-6,15-dimethyl-8,17-diphenyldibenzo[b,i][l,4,8,1 l]tetraazacyclotetradecine, H2L') are redox active as indicated by cyclovoltammetric measurements and confirmed by preparative methods: Reversible oxidation to the corresp...

A new series of oxovanadium (IV) tetraazamacrocyclic complexes type [VO(mac)]SO4, have been synthesized via in situ reaction 1,8-diaminonaphthalene and substituted β-diketones (1-phenyl-3-(phenyl/4-chlorophenyl/4-hydroxyphenyl/4- methoxyphenyl/4-nitrophenyl)-diketone) the presence oxovanadium(IV) sulphate methanol. Attempts to synthesize corresponding metal free macrocyclic ligands did not prov...

New Oxovanadium(IV) and zirconium (IV) complexes were synthesized with tridentate ligand and characterized by elemental analysis, molar conductance measurements, molecular weight determinations, IR, electronic, and H NMR studies. The Oxovanadium(IV) complex is non-electrolyte whereas zirconium(IV) complex is 1:2 electrolytes in nature and may be formulated as[(VOL)2SO4] and [ZrL2]Cl2 respective...

Oxovanadium(IV), manganese(II) and copper(II) complexes of a Schiff base ligand derived from 2,4-dihydroxyacetophenone and 1,2-diaminocyclohexane have been encapsulated in the nanocavity of zeolite-Y by flexible ligand method and characterized by metal analysis, IR spectroscopic studies and X-ray diffraction patterns. The encapsulated complexes abbreviated here as CuL-Y, MnL-Y and VOL-Y catalyz...

Z. Naturforsch. 56 b, 263-270 (2001); received July 27, 2000 Tridentate Salicylaldiminates, ESR, Catalytic Activity Several new binuclear nickel(II), oxovanadium(IV) and palladium(II) complexes (MLX) of tridentate salicylaldimines (LXH2) obtained from substituted salicylaldehydes and 2,4-di-tertbutyl-6-aminophenol, as well as mononuclear nickel(II) and oxovanadium(IV), MQx nH20, complexes with ...

BACKGROUND The oxidative transformation of benzoin to benzil has been accomplished by the use of a wide variety of reagents or catalysts and different reaction procedures. The conventional oxidizing agents yielded mainly benzaldehyde or/and benzoic acid and only a trace amount of benzil. The limits of practical utilization of these reagents involves the use of stoichiometric amounts of corrosiv...