<b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b>
Two new physiologically active ligands, N’-2-[(<i>E</i>)-1-hydroxy-4-methyl-2-oxo-2H-8-chromenyl) ethylidene)-2-furan carbohydrazide (HMCFCH) and N’-2-[(<i>Z</i>)-1-(4-hydroxy-6-methyl-2-oxo-2H-pyranyl) ethylidene]-furan carbohydrazide (HMPFCH) and their VO(II), Mn(II), Fe(II...
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doaj-0756218a03dd44cbb8c50157811af9952020-11-25T01:17:54ZengChemical Society of EthiopiaBulletin of the Chemical Society of Ethiopia1011-39241726-801X2007-04-012116373<b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b>P. Venkateswar RaoK. AshwiniS. AmmaniTwo new physiologically active ligands, N’-2-[(<i>E</i>)-1-hydroxy-4-methyl-2-oxo-2H-8-chromenyl) ethylidene)-2-furan carbohydrazide (HMCFCH) and N’-2-[(<i>Z</i>)-1-(4-hydroxy-6-methyl-2-oxo-2H-pyranyl) ethylidene]-furan carbohydrazide (HMPFCH) and their VO(II), Mn(II), Fe(II), Co(II), Ni(II) and Cu(II) complexes have been prepared. The ligands and the metal complexes have been characterized by elemental analyses, electrical conductance, magnetic susceptibility measurements, UV-Vis, IR, and ESR spectroscopic data. Basing on the above data, Fe(II) and Co(II) complexes of HMCFCH and HMPFCH have been assigned a dimeric octahedral geometry. VO(II) complexes of HMCFCH and HMPFCH have been assigned sulfate bridged dimeric square pyramidal geometry. Mn(II) complex of HMCFCH has been assigned a dimeric octahedral geometry, where as Mn(II) complex of HMPFCH has been ascribed to monomeric octahedral geometry. Cu(II) and Ni(II) complexes of HMCFCH have been ascribed to a polymeric structure. Ni(II) complex of HMPFCH has been assigned a dimeric square planar geometry. Cu(II) complex of HMPFCH has been proposed an octahedral geometry. The ligands and their metal chelates were screened against <i>S. aureus</i> and <i>P. aeruginosa</i>. The ligands and the metal complexes have been found to be active against these microorganisms. The ligands show more activity than the metal complexes.http://www.ajol.info/index.php/bcse/article/view/61372N’-2-(<i>E</i>)-1-hydroxy-4-methyl-2-oxo-2H-8-chromenyl) ethylidene)-2-furan carbohydrazide (HMCFCH)N’-2-[(<i>Z</i>)-1-(4-hydroxy-6-methyl-2-oxo-2H-pyranyl) ethylidene]-furan carbohydrazide (HMPFCH)3-Acetyl-6-methyl-2H-pyran-24(3H)-dione8-Acetyl-4-methyl-UmbelliferoneFuroic acid hydrazideAnti microbial activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
P. Venkateswar Rao K. Ashwini S. Ammani |
spellingShingle |
P. Venkateswar Rao K. Ashwini S. Ammani <b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b> Bulletin of the Chemical Society of Ethiopia N’-2-(<i>E</i>)-1-hydroxy-4-methyl-2-oxo-2H-8-chromenyl) ethylidene)-2-furan carbohydrazide (HMCFCH) N’-2-[(<i>Z</i>)-1-(4-hydroxy-6-methyl-2-oxo-2H-pyranyl) ethylidene]-furan carbohydrazide (HMPFCH) 3-Acetyl-6-methyl-2H-pyran-2 4(3H)-dione 8-Acetyl-4-methyl-Umbelliferone Furoic acid hydrazide Anti microbial activity |
author_facet |
P. Venkateswar Rao K. Ashwini S. Ammani |
author_sort |
P. Venkateswar Rao |
title |
<b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b> |
title_short |
<b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b> |
title_full |
<b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b> |
title_fullStr |
<b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b> |
title_full_unstemmed |
<b>Synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b> |
title_sort |
<b>synthesis and characterization of transition metal complexes derived from some biologically active furoic acid hydrazones</b> |
publisher |
Chemical Society of Ethiopia |
series |
Bulletin of the Chemical Society of Ethiopia |
issn |
1011-3924 1726-801X |
publishDate |
2007-04-01 |
description |
Two new physiologically active ligands, N’-2-[(<i>E</i>)-1-hydroxy-4-methyl-2-oxo-2H-8-chromenyl) ethylidene)-2-furan carbohydrazide (HMCFCH) and N’-2-[(<i>Z</i>)-1-(4-hydroxy-6-methyl-2-oxo-2H-pyranyl) ethylidene]-furan carbohydrazide (HMPFCH) and their VO(II), Mn(II), Fe(II), Co(II), Ni(II) and Cu(II) complexes have been prepared. The ligands and the metal complexes have been characterized by elemental analyses, electrical conductance, magnetic susceptibility measurements, UV-Vis, IR, and ESR spectroscopic data. Basing on the above data, Fe(II) and Co(II) complexes of HMCFCH and HMPFCH have been assigned a dimeric octahedral geometry. VO(II) complexes of HMCFCH and HMPFCH have been assigned sulfate bridged dimeric square pyramidal geometry. Mn(II) complex of HMCFCH has been assigned a dimeric octahedral geometry, where as Mn(II) complex of HMPFCH has been ascribed to monomeric octahedral geometry. Cu(II) and Ni(II) complexes of HMCFCH have been ascribed to a polymeric structure. Ni(II) complex of HMPFCH has been assigned a dimeric square planar geometry. Cu(II) complex of HMPFCH has been proposed an octahedral geometry. The ligands and their metal chelates were screened against <i>S. aureus</i> and <i>P. aeruginosa</i>. The ligands and the metal complexes have been found to be active against these microorganisms. The ligands show more activity than the metal complexes. |
topic |
N’-2-(<i>E</i>)-1-hydroxy-4-methyl-2-oxo-2H-8-chromenyl) ethylidene)-2-furan carbohydrazide (HMCFCH) N’-2-[(<i>Z</i>)-1-(4-hydroxy-6-methyl-2-oxo-2H-pyranyl) ethylidene]-furan carbohydrazide (HMPFCH) 3-Acetyl-6-methyl-2H-pyran-2 4(3H)-dione 8-Acetyl-4-methyl-Umbelliferone Furoic acid hydrazide Anti microbial activity |
url |
http://www.ajol.info/index.php/bcse/article/view/61372 |
work_keys_str_mv |
AT pvenkateswarrao bsynthesisandcharacterizationoftransitionmetalcomplexesderivedfromsomebiologicallyactivefuroicacidhydrazonesb AT kashwini bsynthesisandcharacterizationoftransitionmetalcomplexesderivedfromsomebiologicallyactivefuroicacidhydrazonesb AT sammani bsynthesisandcharacterizationoftransitionmetalcomplexesderivedfromsomebiologicallyactivefuroicacidhydrazonesb |
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