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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
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