Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP)

Five new organotin(IV) complexes of ortho-vanillin- 2-hydrazinopyridine hydrazone with formula [RnSn- Cl4–n(VHP)] [R = Me2, n = 2 (2); R = Ph2, n = 2 (3); R= nBu2, n = 2 (4); R = nBu, n = 2 (5) and R = 1, n = 0 (6)] have been synthesized by direct reaction of orthovanillin- 2-hydrazinopyridine...

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Main Authors: Norrihan, Sam, Md. Abu, Affan, Abdus, Salam, Mohd Razip, Asaruddin
Format: Article
Language:English
Published: OJIC 2012
Subjects:
Online Access:http://ir.unimas.my/id/eprint/14384/
http://ir.unimas.my/id/eprint/14384/1/Norrihan.pdf
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author Norrihan, Sam
Md. Abu, Affan
Abdus, Salam
Mohd Razip, Asaruddin
author_facet Norrihan, Sam
Md. Abu, Affan
Abdus, Salam
Mohd Razip, Asaruddin
author_sort Norrihan, Sam
building UNIMAS Institutional Repository
collection Online Access
description Five new organotin(IV) complexes of ortho-vanillin- 2-hydrazinopyridine hydrazone with formula [RnSn- Cl4–n(VHP)] [R = Me2, n = 2 (2); R = Ph2, n = 2 (3); R= nBu2, n = 2 (4); R = nBu, n = 2 (5) and R = 1, n = 0 (6)] have been synthesized by direct reaction of orthovanillin- 2-hydrazinopyridine hydrazone [(VHP), (1)], base and organotin(IV) chloride(s) in absolute methanol. The hydrazone ligand [(VHP), (1)] and its organotin( IV) complexes (2-6) have been characterized by UV-Visible, FT-IR and 1H NMR spectral studies. Spectroscopic data suggested that in the complexes (2-4), the ligand (1) acted as a neutral bidentate ligand and is coordinated to the tin(IV) atom via the azomethine nitrogen and pyridyl nitrogen atoms, whereas the ligand (1) acted as a uninegative tridentate ligand and coordinated to the tin(IV) atom through phenolic- O, azomethine-N and pyridyl-N atoms in complexes (5-6). The toxicity of the ligand (1) and its organotin (IV) complexes (2-6) were determined against Artemia salina. Organotin(IV) complexes showed moderate activity against Artemia salina. The ligand (1) and its organotin(IV) complexes (2-6) were also tested against four types of bacteria namely Bacillus cereus, Staphylococcus aureus, Escherichia coli and Enterobacter aerogenes. All organotin(IV) complexes and the free ligand (1) showed better antibacterial activities against bacteria. Among the organotin(IV) complexes (2-6), diphenyltin(IV) complex (3) showed higher activity against the four types of bacteria.
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spelling unimas-143842022-01-24T06:24:07Z http://ir.unimas.my/id/eprint/14384/ Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP) Norrihan, Sam Md. Abu, Affan Abdus, Salam Mohd Razip, Asaruddin QD Chemistry Five new organotin(IV) complexes of ortho-vanillin- 2-hydrazinopyridine hydrazone with formula [RnSn- Cl4–n(VHP)] [R = Me2, n = 2 (2); R = Ph2, n = 2 (3); R= nBu2, n = 2 (4); R = nBu, n = 2 (5) and R = 1, n = 0 (6)] have been synthesized by direct reaction of orthovanillin- 2-hydrazinopyridine hydrazone [(VHP), (1)], base and organotin(IV) chloride(s) in absolute methanol. The hydrazone ligand [(VHP), (1)] and its organotin( IV) complexes (2-6) have been characterized by UV-Visible, FT-IR and 1H NMR spectral studies. Spectroscopic data suggested that in the complexes (2-4), the ligand (1) acted as a neutral bidentate ligand and is coordinated to the tin(IV) atom via the azomethine nitrogen and pyridyl nitrogen atoms, whereas the ligand (1) acted as a uninegative tridentate ligand and coordinated to the tin(IV) atom through phenolic- O, azomethine-N and pyridyl-N atoms in complexes (5-6). The toxicity of the ligand (1) and its organotin (IV) complexes (2-6) were determined against Artemia salina. Organotin(IV) complexes showed moderate activity against Artemia salina. The ligand (1) and its organotin(IV) complexes (2-6) were also tested against four types of bacteria namely Bacillus cereus, Staphylococcus aureus, Escherichia coli and Enterobacter aerogenes. All organotin(IV) complexes and the free ligand (1) showed better antibacterial activities against bacteria. Among the organotin(IV) complexes (2-6), diphenyltin(IV) complex (3) showed higher activity against the four types of bacteria. OJIC 2012 Article PeerReviewed text en http://ir.unimas.my/id/eprint/14384/1/Norrihan.pdf Norrihan, Sam and Md. Abu, Affan and Abdus, Salam and Mohd Razip, Asaruddin (2012) Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP). Open Journal of Inorganic Chemistry, 2. pp. 22-27. ISSN 2161-7414 https://www.researchgate.net/publication/266593201_Synthesis_spectral_characterization_and_biological_activities_of_OrganotinIV_complexes_with_ortho-vanillin-2-hydrazinopyridine_VHP doi:10.4236/ojic.2012.22004
spellingShingle QD Chemistry
Norrihan, Sam
Md. Abu, Affan
Abdus, Salam
Mohd Razip, Asaruddin
Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP)
title Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP)
title_full Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP)
title_fullStr Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP)
title_full_unstemmed Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP)
title_short Synthesis, spectral characterization and biological activities of Organotin(IV) complexes with ortho-vanillin-2-hydrazinopyridine (VHP)
title_sort synthesis, spectral characterization and biological activities of organotin(iv) complexes with ortho-vanillin-2-hydrazinopyridine (vhp)
topic QD Chemistry
url http://ir.unimas.my/id/eprint/14384/
http://ir.unimas.my/id/eprint/14384/
http://ir.unimas.my/id/eprint/14384/
http://ir.unimas.my/id/eprint/14384/1/Norrihan.pdf