Novel Biologically Potent Diorganosilicon(IV) Complexes of Indole-2,3-Dione Derivatives
The aim of the present study is to synthesize some novel ecofriendly fungicides and bactericides of indole-2,3-dione derivatives, having important pharmacodynamic significance. The ligands used in the present account are derived by the condensation of 1,3-dihydro-3-[2-(phenyl)-2-oxoethylidene]-2H-in...
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| Format: | Article |
| Language: | English |
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Wiley
2005-01-01
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| Series: | Bioinorganic Chemistry and Applications |
| Online Access: | http://dx.doi.org/10.1155/BCA.2005.255 |
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| author | R. V. Singh Pooja Nagpal |
| author_facet | R. V. Singh Pooja Nagpal |
| author_sort | R. V. Singh |
| collection | DOAJ |
| description | The aim of the present study is to synthesize some novel ecofriendly fungicides and bactericides of
indole-2,3-dione derivatives, having important pharmacodynamic significance. The ligands used in the
present account are derived by the condensation of 1,3-dihydro-3-[2-(phenyl)-2-oxoethylidene]-2H-indol-2-
one, 1,3-dihydro-3-[2-(4-nitrophenyl)-2-oxoethylidene]-2H-indol-2-one and 1,3-dihydro-3-[2-(4-nitro-3-methylphenyl)-
2-oxoethylidene]-2H-indol-2-one with hydrazinecarboxamide and hydrazinecarbothioamide. These
imines, on interaction with diorganosilicon(IV) chlorides, yield complexes having Si–O or Si–S and Si←N
bonds. The structure of these compounds have been elucidated by elemental microanalyses and spectral
[(UV), (IR), 1H, 13C and 29Si NMR)] studies which unerringly point to a trigonal bipyramidal and octahedral
geometries for unimolar and bimolar reactions, respectively. The potency of the synthesized compounds have
been assessed by growth inhibiting potential of the complexes against variety of fungal and bacterial strains
and male albino rats. The results of these biological studies have been compared with the standard fungicide,
Bavistin. The studies demonstrate that, 1,3-dihydro-3-[2-(4-nitrophenyl)-2-oxoethylidene]-2H-indol-2-onehydrazincarbothioamide
and its diphenylsilicon(IV) complexes have comparable antimicrobial activity and
are less toxic to male albino rats than Bavistin. |
| format | Article |
| id | doaj-art-0d9928f277e04c55804d6eff96785b41 |
| institution | Kabale University |
| issn | 1565-3633 |
| language | English |
| publishDate | 2005-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Bioinorganic Chemistry and Applications |
| spelling | doaj-art-0d9928f277e04c55804d6eff96785b412025-02-03T06:12:55ZengWileyBioinorganic Chemistry and Applications1565-36332005-01-0133-425527010.1155/BCA.2005.255Novel Biologically Potent Diorganosilicon(IV) Complexes of Indole-2,3-Dione DerivativesR. V. Singh0Pooja Nagpal1Department of Chemistry, University of Rajasthan, Jaipur 302 004, IndiaDepartment of Chemistry, University of Rajasthan, Jaipur 302 004, IndiaThe aim of the present study is to synthesize some novel ecofriendly fungicides and bactericides of indole-2,3-dione derivatives, having important pharmacodynamic significance. The ligands used in the present account are derived by the condensation of 1,3-dihydro-3-[2-(phenyl)-2-oxoethylidene]-2H-indol-2- one, 1,3-dihydro-3-[2-(4-nitrophenyl)-2-oxoethylidene]-2H-indol-2-one and 1,3-dihydro-3-[2-(4-nitro-3-methylphenyl)- 2-oxoethylidene]-2H-indol-2-one with hydrazinecarboxamide and hydrazinecarbothioamide. These imines, on interaction with diorganosilicon(IV) chlorides, yield complexes having Si–O or Si–S and Si←N bonds. The structure of these compounds have been elucidated by elemental microanalyses and spectral [(UV), (IR), 1H, 13C and 29Si NMR)] studies which unerringly point to a trigonal bipyramidal and octahedral geometries for unimolar and bimolar reactions, respectively. The potency of the synthesized compounds have been assessed by growth inhibiting potential of the complexes against variety of fungal and bacterial strains and male albino rats. The results of these biological studies have been compared with the standard fungicide, Bavistin. The studies demonstrate that, 1,3-dihydro-3-[2-(4-nitrophenyl)-2-oxoethylidene]-2H-indol-2-onehydrazincarbothioamide and its diphenylsilicon(IV) complexes have comparable antimicrobial activity and are less toxic to male albino rats than Bavistin.http://dx.doi.org/10.1155/BCA.2005.255 |
| spellingShingle | R. V. Singh Pooja Nagpal Novel Biologically Potent Diorganosilicon(IV) Complexes of Indole-2,3-Dione Derivatives Bioinorganic Chemistry and Applications |
| title | Novel Biologically Potent Diorganosilicon(IV) Complexes
of Indole-2,3-Dione Derivatives |
| title_full | Novel Biologically Potent Diorganosilicon(IV) Complexes
of Indole-2,3-Dione Derivatives |
| title_fullStr | Novel Biologically Potent Diorganosilicon(IV) Complexes
of Indole-2,3-Dione Derivatives |
| title_full_unstemmed | Novel Biologically Potent Diorganosilicon(IV) Complexes
of Indole-2,3-Dione Derivatives |
| title_short | Novel Biologically Potent Diorganosilicon(IV) Complexes
of Indole-2,3-Dione Derivatives |
| title_sort | novel biologically potent diorganosilicon iv complexes of indole 2 3 dione derivatives |
| url | http://dx.doi.org/10.1155/BCA.2005.255 |
| work_keys_str_mv | AT rvsingh novelbiologicallypotentdiorganosiliconivcomplexesofindole23dionederivatives AT poojanagpal novelbiologicallypotentdiorganosiliconivcomplexesofindole23dionederivatives |