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Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms

Twelve new organotin(IV) complexes of the type RnSnLm [where n = 3, m = 1, R = CH(3) or C(6)H(5); n = 2, m = 2, R = C(6)H(5) or C(4)H(9) ; L = anion of Schiff bases derived from the condensation of 2-amino-5-(o-anisyl)-l,3,4-thiadiazole with salicylaldehyde (HL-1), 2- hydroxynaphthaldehyde (HL-2) an...

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Autores principales: Nath, Mala, Goyal, Savita
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364992/
https://www.ncbi.nlm.nih.gov/pubmed/18472781
http://dx.doi.org/10.1155/MBD.1995.297
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author Nath, Mala
Goyal, Savita
author_facet Nath, Mala
Goyal, Savita
author_sort Nath, Mala
collection PubMed
description Twelve new organotin(IV) complexes of the type RnSnLm [where n = 3, m = 1, R = CH(3) or C(6)H(5); n = 2, m = 2, R = C(6)H(5) or C(4)H(9) ; L = anion of Schiff bases derived from the condensation of 2-amino-5-(o-anisyl)-l,3,4-thiadiazole with salicylaldehyde (HL-1), 2- hydroxynaphthaldehyde (HL-2) and 2-hydroxyacetophenone (HL-3)] have been synthesized and characterized by elemental analysis, molar conductances, electronic, infrared, far-infrared, (1)H NMR and (119)Sn Mössbauer spectral studies. Thermal studies of two complexes, viz., Ph(3)Sn (L-1) and Ph(2)Sn(L-2)(2) have been carried out in the temperature range 25-1000∘C using TG, DTG and DTA techniques. All these complexes decompose gradually with the formation of SnO(2) as an end product. In vitro antimicrobial activity of the Schiff bases and their complexes has also been determined against Streptococcus faecalis, Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus Penicillin resistance (2500 units), Candida albicans, Cryptococcus neoformans, Sporotrichum schenckii, Trichophyton mentagrophytes and Aspergillus fumigatus. The Schiff bases (HL-1), (HL-2) and the organotin(IV) compounds have also been tested against various important herbicidal, fungicidal, insecticidal species and also for parasitological activity against freeliving nematode.
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spelling pubmed-23649922008-05-12 Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms Nath, Mala Goyal, Savita Met Based Drugs Research Article Twelve new organotin(IV) complexes of the type RnSnLm [where n = 3, m = 1, R = CH(3) or C(6)H(5); n = 2, m = 2, R = C(6)H(5) or C(4)H(9) ; L = anion of Schiff bases derived from the condensation of 2-amino-5-(o-anisyl)-l,3,4-thiadiazole with salicylaldehyde (HL-1), 2- hydroxynaphthaldehyde (HL-2) and 2-hydroxyacetophenone (HL-3)] have been synthesized and characterized by elemental analysis, molar conductances, electronic, infrared, far-infrared, (1)H NMR and (119)Sn Mössbauer spectral studies. Thermal studies of two complexes, viz., Ph(3)Sn (L-1) and Ph(2)Sn(L-2)(2) have been carried out in the temperature range 25-1000∘C using TG, DTG and DTA techniques. All these complexes decompose gradually with the formation of SnO(2) as an end product. In vitro antimicrobial activity of the Schiff bases and their complexes has also been determined against Streptococcus faecalis, Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus Penicillin resistance (2500 units), Candida albicans, Cryptococcus neoformans, Sporotrichum schenckii, Trichophyton mentagrophytes and Aspergillus fumigatus. The Schiff bases (HL-1), (HL-2) and the organotin(IV) compounds have also been tested against various important herbicidal, fungicidal, insecticidal species and also for parasitological activity against freeliving nematode. Hindawi Publishing Corporation 1995 /pmc/articles/PMC2364992/ /pubmed/18472781 http://dx.doi.org/10.1155/MBD.1995.297 Text en Copyright © 1995 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nath, Mala
Goyal, Savita
Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms
title Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms
title_full Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms
title_fullStr Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms
title_full_unstemmed Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms
title_short Spectral Studies and Bactericidal, Fungicidal, Insecticidal and Parasitological Activities of Organotin(IV) Complexes of Thio Schiff Bases Having no Donor Atoms
title_sort spectral studies and bactericidal, fungicidal, insecticidal and parasitological activities of organotin(iv) complexes of thio schiff bases having no donor atoms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364992/
https://www.ncbi.nlm.nih.gov/pubmed/18472781
http://dx.doi.org/10.1155/MBD.1995.297
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