Synthesis, Characterization and Antitumor Activity of Some New Oganotellurium Compounds Containing Azomethine Group, Part One
DOI:
https://doi.org/10.24297/jac.v8i1.4027Keywords:
Schiff-base, 3, 4-dihydroxy benzaldehyde, Tellurium tetrabromide, HSQC- NMR, AntitumorAbstract
New tellurated schiff bases were synthesized by the reaction of the corresponding mercurated Schiff  bases compounds A1-A3 with tellurium tetrabromide in 1:1 mole ratio and  that  gave organyltellurium tribromides  A4-A6.  On the other hand, when mercurated schiff bases and tellurium tetrabromide brought  together in 2:1 mole ratio gave diorganyltellurium dibromides compounds A10-A12 followed by reduction with hydrazine hydrate gave new diorganyl tellurides A13-A15. Reduction of compounds A4-A6 by hydrazine hydrate gave new ditellurides A7-A9.  All compounds were characterized by elemental analysis, IR, 1H , 13C NMR, HSQC-NMR and mass spectra. Invitro anti-tumor bioactivity of some compounds were tested.Â
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