Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands

<p>Three bidentate Schiff bases having nitrogen and sulphur donor sequences were prepared by condensing S-benzyldithiocarbazate (<mml:math alttext="chem{NH_2NHCS_2CH_2C_6H_5}"> <mml:msub> <mml:mtext>NH</mml:mtext> <mml:mn>2</mml:mn> </mml:...

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Language:English
Published: Wiley 2006-01-01
Series:Bioinorganic Chemistry and Applications
Online Access:http://www.hindawi.com/GetArticle.aspx?doi=10.1155/BCA/2006/23245
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description <p>Three bidentate Schiff bases having nitrogen and sulphur donor sequences were prepared by condensing S-benzyldithiocarbazate (<mml:math alttext="chem{NH_2NHCS_2CH_2C_6H_5}"> <mml:msub> <mml:mtext>NH</mml:mtext> <mml:mn>2</mml:mn> </mml:msub> <mml:msub> <mml:mtext>NHCS</mml:mtext> <mml:mn>2</mml:mn> </mml:msub> <mml:msub> <mml:mtext>CH</mml:mtext> <mml:mn>2</mml:mn> </mml:msub> <mml:msub> <mml:mtext>C</mml:mtext> <mml:mn>6</mml:mn> </mml:msub> <mml:msub> <mml:mtext>H</mml:mtext> <mml:mn>5</mml:mn> </mml:msub> </mml:math>) with heterocyclic aldehydes. The reaction of diphenyltin dichloride with Schiff bases leads to the formation of a new series of organotin(IV) complexes. An attempt has been made to prove their structures on the basis of elemental analyses, conductance measurements, molecular weights determinations, UV, infrared, and multinuclear magnetic resonance (<mml:math alttext="chem{^{1}H}"> <mml:mmultiscripts> <mml:mtext>H</mml:mtext> <mml:mprescripts/> <mml:none/> <mml:mn>1</mml:mn> </mml:mmultiscripts> </mml:math>, <mml:math alttext="chem{^{13}C}"> <mml:mmultiscripts> <mml:mtext>C</mml:mtext> <mml:mprescripts/> <mml:none/> <mml:mrow> <mml:mn>13</mml:mn> </mml:mrow> </mml:mmultiscripts> </mml:math>, and <mml:math alttext="chem{^{119}Sn}"> <mml:mmultiscripts> <mml:mtext>S</mml:mtext> <mml:mprescripts/> <mml:none/> <mml:mrow> <mml:mn>119</mml:mn> </mml:mrow> </mml:mmultiscripts> <mml:mtext>n</mml:mtext> </mml:math>) spectral studies. Organotin(IV) complexes were five- and six-coordinate. Schiff bases and their corresponding organotin complexes have also been screened for their antibacterial and antifungal activities and found to be quite active in this respect.</p>
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spelling doaj-art-c030d3a70f824098b45abc5ed2b0805c2025-02-03T05:58:38ZengWileyBioinorganic Chemistry and Applications1565-36332006-01-012006Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands<p>Three bidentate Schiff bases having nitrogen and sulphur donor sequences were prepared by condensing S-benzyldithiocarbazate (<mml:math alttext="chem{NH_2NHCS_2CH_2C_6H_5}"> <mml:msub> <mml:mtext>NH</mml:mtext> <mml:mn>2</mml:mn> </mml:msub> <mml:msub> <mml:mtext>NHCS</mml:mtext> <mml:mn>2</mml:mn> </mml:msub> <mml:msub> <mml:mtext>CH</mml:mtext> <mml:mn>2</mml:mn> </mml:msub> <mml:msub> <mml:mtext>C</mml:mtext> <mml:mn>6</mml:mn> </mml:msub> <mml:msub> <mml:mtext>H</mml:mtext> <mml:mn>5</mml:mn> </mml:msub> </mml:math>) with heterocyclic aldehydes. The reaction of diphenyltin dichloride with Schiff bases leads to the formation of a new series of organotin(IV) complexes. An attempt has been made to prove their structures on the basis of elemental analyses, conductance measurements, molecular weights determinations, UV, infrared, and multinuclear magnetic resonance (<mml:math alttext="chem{^{1}H}"> <mml:mmultiscripts> <mml:mtext>H</mml:mtext> <mml:mprescripts/> <mml:none/> <mml:mn>1</mml:mn> </mml:mmultiscripts> </mml:math>, <mml:math alttext="chem{^{13}C}"> <mml:mmultiscripts> <mml:mtext>C</mml:mtext> <mml:mprescripts/> <mml:none/> <mml:mrow> <mml:mn>13</mml:mn> </mml:mrow> </mml:mmultiscripts> </mml:math>, and <mml:math alttext="chem{^{119}Sn}"> <mml:mmultiscripts> <mml:mtext>S</mml:mtext> <mml:mprescripts/> <mml:none/> <mml:mrow> <mml:mn>119</mml:mn> </mml:mrow> </mml:mmultiscripts> <mml:mtext>n</mml:mtext> </mml:math>) spectral studies. Organotin(IV) complexes were five- and six-coordinate. Schiff bases and their corresponding organotin complexes have also been screened for their antibacterial and antifungal activities and found to be quite active in this respect.</p>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/BCA/2006/23245
spellingShingle Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands
Bioinorganic Chemistry and Applications
title Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands
title_full Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands
title_fullStr Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands
title_full_unstemmed Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands
title_short Synthetic, Structural, and Biochemical Studies of Organotin(IV) With Schiff Bases Having Nitrogen and Sulphur Donor Ligands
title_sort synthetic structural and biochemical studies of organotin iv with schiff bases having nitrogen and sulphur donor ligands
url http://www.hindawi.com/GetArticle.aspx?doi=10.1155/BCA/2006/23245