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Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide

The reactions of tetraethylthiouram disulfide (DTS), an inhibitor of the nephrotoxicity of Pt(II) drugs, an efficient agent in the treatment of chronic alcoholism, in the treatment of HIV infections, AIDS and heavy metal toxicity, and a fungicide and herbicide, with K(2)[PtCl(4)], in ratio 1:1 and 1...

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Autores principales: Cervantes, G., Moreno, V., Molins, E., Miravitlles, C.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365086/
https://www.ncbi.nlm.nih.gov/pubmed/18475812
http://dx.doi.org/10.1155/MBD.1997.317
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author Cervantes, G.
Moreno, V.
Molins, E.
Miravitlles, C.
author_facet Cervantes, G.
Moreno, V.
Molins, E.
Miravitlles, C.
author_sort Cervantes, G.
collection PubMed
description The reactions of tetraethylthiouram disulfide (DTS), an inhibitor of the nephrotoxicity of Pt(II) drugs, an efficient agent in the treatment of chronic alcoholism, in the treatment of HIV infections, AIDS and heavy metal toxicity, and a fungicide and herbicide, with K(2)[PtCl(4)], in ratio 1:1 and 1:2, gave the compounds [PtCl(2)DTS] and [Pt(S(2)CNEt(2))(2)] respectively. The reaction of the complexes K(2)[PdCl(4)], Pd(AcO)(2) and [PdCl(2)(PhCN)(2)], where PhCN = Benzonitrile, with tetraethylthiouram disulfide in ratio 1:1 or 1:2, yielded orange crystals identified as [Pd(S(2)CNEt(2))(2)]. The crystals were suitable for study by X-ray diffraction. The -S-S- bridge in the tetraethylthiouram disulfude molecule was broken and the two molecules of the thiocarbamate derivative were bound to the Pd(II) by the equivalents sulfur atoms. All the compounds were characterized by IR, (1)H and (13)C NMR spectroscopies.
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spelling pubmed-23650862008-05-12 Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide Cervantes, G. Moreno, V. Molins, E. Miravitlles, C. Met Based Drugs Research Article The reactions of tetraethylthiouram disulfide (DTS), an inhibitor of the nephrotoxicity of Pt(II) drugs, an efficient agent in the treatment of chronic alcoholism, in the treatment of HIV infections, AIDS and heavy metal toxicity, and a fungicide and herbicide, with K(2)[PtCl(4)], in ratio 1:1 and 1:2, gave the compounds [PtCl(2)DTS] and [Pt(S(2)CNEt(2))(2)] respectively. The reaction of the complexes K(2)[PdCl(4)], Pd(AcO)(2) and [PdCl(2)(PhCN)(2)], where PhCN = Benzonitrile, with tetraethylthiouram disulfide in ratio 1:1 or 1:2, yielded orange crystals identified as [Pd(S(2)CNEt(2))(2)]. The crystals were suitable for study by X-ray diffraction. The -S-S- bridge in the tetraethylthiouram disulfude molecule was broken and the two molecules of the thiocarbamate derivative were bound to the Pd(II) by the equivalents sulfur atoms. All the compounds were characterized by IR, (1)H and (13)C NMR spectroscopies. Hindawi Publishing Corporation 1997 /pmc/articles/PMC2365086/ /pubmed/18475812 http://dx.doi.org/10.1155/MBD.1997.317 Text en Copyright © 1997 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
Cervantes, G.
Moreno, V.
Molins, E.
Miravitlles, C.
Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide
title Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide
title_full Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide
title_fullStr Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide
title_full_unstemmed Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide
title_short Reactions of Pd(II) and Pt(II) Complexes With Tetraethylthiouram Disulfide
title_sort reactions of pd(ii) and pt(ii) complexes with tetraethylthiouram disulfide
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365086/
https://www.ncbi.nlm.nih.gov/pubmed/18475812
http://dx.doi.org/10.1155/MBD.1997.317
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