2016
DOI: 10.24297/jac.v8i1.4027
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Synthesis, Characterization and Antitumor Activity of Some New Oganotellurium Compounds Containing Azomethine Group, Part One

Abstract: 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 … Show more

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Cited by 4 publications
(3 citation statements)
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“…λ 4 -tellanyl)benzenesulfonic acid 2 (1.79 g, 4 mmol) of tellurium tetrabromide was mixed with an equivalent molar amount of (2-amino-5-sulfophenyl) mercury(II)chloride 1 weighing 1.63 g., 4 mmol in 40 mL of 1,4-dioxane and refluxed for 6 hours under argon atmosphere. Upon cooling, a 1:2 addition compound of mercury(II) halide and dioxane was isolated as white sheets and filtered.…”
Section: -Amino-3-(tribromo-mentioning
confidence: 99%
See 1 more Smart Citation
“…λ 4 -tellanyl)benzenesulfonic acid 2 (1.79 g, 4 mmol) of tellurium tetrabromide was mixed with an equivalent molar amount of (2-amino-5-sulfophenyl) mercury(II)chloride 1 weighing 1.63 g., 4 mmol in 40 mL of 1,4-dioxane and refluxed for 6 hours under argon atmosphere. Upon cooling, a 1:2 addition compound of mercury(II) halide and dioxane was isolated as white sheets and filtered.…”
Section: -Amino-3-(tribromo-mentioning
confidence: 99%
“…Synthesising several organotellurium compounds using transmetallation of organomercury substances has been widely studied and reported in several publications [4][5][6][7]. Aromatic compounds, when reacting with tellurium tetrahalides, undergo a direct substitution reaction, and the obtained yield is low.…”
Section: Introductionmentioning
confidence: 99%
“…The compounds a1-a10 were prepared according to previously published procedure [13,14]. Infrared spectra were recorded as KBr discs in the range of 4000-400 cm -1 using a Shimadzu FT-IR spectrophotometer at Department of Chemistry, College of Education for Pure Sciences, University of Basrah, Iraq.…”
Section: Instrumentation and Materialsmentioning
confidence: 99%