Cargando…
Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions
[Image: see text] Hypervalent tellurium compounds (telluranes) are promising therapeutical agents with negligible toxicities for some diseases in animal models. The C–Te bond of organotellurium compounds is commonly considered unstable, disfavoring their applicability in biological studies. In this...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641895/ https://www.ncbi.nlm.nih.gov/pubmed/31457735 http://dx.doi.org/10.1021/acsomega.7b00628 |
_version_ | 1783436878572158976 |
---|---|
author | Princival, Cleverson R. Archilha, Marcos V. L. R. Dos Santos, Alcindo A. Franco, Maurício P. Braga, Ataualpa A. C. Rodrigues-Oliveira, André F. Correra, Thiago C. Cunha, Rodrigo L. O. R. Comasseto, João V. |
author_facet | Princival, Cleverson R. Archilha, Marcos V. L. R. Dos Santos, Alcindo A. Franco, Maurício P. Braga, Ataualpa A. C. Rodrigues-Oliveira, André F. Correra, Thiago C. Cunha, Rodrigo L. O. R. Comasseto, João V. |
author_sort | Princival, Cleverson R. |
collection | PubMed |
description | [Image: see text] Hypervalent tellurium compounds (telluranes) are promising therapeutical agents with negligible toxicities for some diseases in animal models. The C–Te bond of organotellurium compounds is commonly considered unstable, disfavoring their applicability in biological studies. In this study, the stability of a set of telluranes composed of an inorganic derivative and noncharged and charged organic derivatives was monitored in aqueous media with (1)H, (13)C, and (125)Te NMR spectroscopy and high-resolution mass spectrometry. Organic telluranes were found to be remarkably resistant and stable to hydrolysis, whereas the inorganic tellurane AS101 is totally converted to the hydrolysis product, trichlorooxytellurate, [TeOCl(3)](−), which was also observed in the hydrolysis of TeCl(4). The noteworthy stability of organotelluranes in aqueous media makes them prone to further structure–activity relationship studies and to be considered for broad biological investigations. |
format | Online Article Text |
id | pubmed-6641895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66418952019-08-27 Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions Princival, Cleverson R. Archilha, Marcos V. L. R. Dos Santos, Alcindo A. Franco, Maurício P. Braga, Ataualpa A. C. Rodrigues-Oliveira, André F. Correra, Thiago C. Cunha, Rodrigo L. O. R. Comasseto, João V. ACS Omega [Image: see text] Hypervalent tellurium compounds (telluranes) are promising therapeutical agents with negligible toxicities for some diseases in animal models. The C–Te bond of organotellurium compounds is commonly considered unstable, disfavoring their applicability in biological studies. In this study, the stability of a set of telluranes composed of an inorganic derivative and noncharged and charged organic derivatives was monitored in aqueous media with (1)H, (13)C, and (125)Te NMR spectroscopy and high-resolution mass spectrometry. Organic telluranes were found to be remarkably resistant and stable to hydrolysis, whereas the inorganic tellurane AS101 is totally converted to the hydrolysis product, trichlorooxytellurate, [TeOCl(3)](−), which was also observed in the hydrolysis of TeCl(4). The noteworthy stability of organotelluranes in aqueous media makes them prone to further structure–activity relationship studies and to be considered for broad biological investigations. American Chemical Society 2017-08-10 /pmc/articles/PMC6641895/ /pubmed/31457735 http://dx.doi.org/10.1021/acsomega.7b00628 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Princival, Cleverson R. Archilha, Marcos V. L. R. Dos Santos, Alcindo A. Franco, Maurício P. Braga, Ataualpa A. C. Rodrigues-Oliveira, André F. Correra, Thiago C. Cunha, Rodrigo L. O. R. Comasseto, João V. Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions |
title | Stability Study of Hypervalent Tellurium Compounds
in Aqueous Solutions |
title_full | Stability Study of Hypervalent Tellurium Compounds
in Aqueous Solutions |
title_fullStr | Stability Study of Hypervalent Tellurium Compounds
in Aqueous Solutions |
title_full_unstemmed | Stability Study of Hypervalent Tellurium Compounds
in Aqueous Solutions |
title_short | Stability Study of Hypervalent Tellurium Compounds
in Aqueous Solutions |
title_sort | stability study of hypervalent tellurium compounds
in aqueous solutions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641895/ https://www.ncbi.nlm.nih.gov/pubmed/31457735 http://dx.doi.org/10.1021/acsomega.7b00628 |
work_keys_str_mv | AT princivalcleversonr stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT archilhamarcosvlr stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT dossantosalcindoa stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT francomauriciop stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT bragaataualpaac stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT rodriguesoliveiraandref stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT correrathiagoc stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT cunharodrigolor stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions AT comassetojoaov stabilitystudyofhypervalenttelluriumcompoundsinaqueoussolutions |