Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1021/acsomega.7b00628 http://repositorio.unifesp.br/handle/11600/51424 |
Resumo: | 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 H-1, C-13, and Te-125 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, [TeOCl3](-), which was also observed in the hydrolysis of TeCl4. 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. |
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Repositório Institucional da UNIFESP |
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Stability Study of Hypervalent Tellurium Compounds in Aqueous SolutionsHypervalent 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 H-1, C-13, and Te-125 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, [TeOCl3](-), which was also observed in the hydrolysis of TeCl4. 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.Univ São Paulo, Inst Quim, BR-05508020 São Paulo, SP, BrazilUniv Fed ABC, Ctr Ciencias Nat & Humanas, BR-09210580 Santo Andre, SP, BrazilUniv Fed São Paulo, Inst Ciencias Ambientais Quim & Farmaceut, BR-04021001 Diadema, SP, BrazilUniv Fed São Paulo, Inst Ciencias Ambientais Quim & Farmaceut, BR-04021001 Diadema, SP, BrazilWeb of ScienceFAPESPCNPqCAPESNAP-CatSinQFAPESP: 2014/15962-5FAPESP: 2015/08539-1CNPq: 487012/2012-7Amer Chemical Soc2019-08-19T11:49:53Z2019-08-19T11:49:53Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion4431-4439application/pdfhttp://dx.doi.org/10.1021/acsomega.7b00628Acs Omega. Washington, v. 2, n. 8, p. 4431-4439, 2017.10.1021/acsomega.7b00628WOS000409924000040.pdf2470-1343http://repositorio.unifesp.br/handle/11600/51424WOS:000409924000040enginfo:eu-repo/semantics/openAccessPrincival, Cleverson R.Archilha, Marcos V. L. R.Dos Santos, Alcindo A.Franco, Mauricio P.Braga, Ataualpa A. C.Rodrigues-Oliveira, Andre F.Correra, Thiago C.Cunha, Rodrigo L. O. R.Comasseto, Joao V. [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-03T02:19:24Zoai:repositorio.unifesp.br/:11600/51424Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-03T02:19:24Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions |
title |
Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions |
spellingShingle |
Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions Princival, Cleverson R. |
title_short |
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_sort |
Stability Study of Hypervalent Tellurium Compounds in Aqueous Solutions |
author |
Princival, Cleverson R. |
author_facet |
Princival, Cleverson R. Archilha, Marcos V. L. R. Dos Santos, Alcindo A. Franco, Mauricio P. Braga, Ataualpa A. C. Rodrigues-Oliveira, Andre F. Correra, Thiago C. Cunha, Rodrigo L. O. R. Comasseto, Joao V. [UNIFESP] |
author_role |
author |
author2 |
Archilha, Marcos V. L. R. Dos Santos, Alcindo A. Franco, Mauricio P. Braga, Ataualpa A. C. Rodrigues-Oliveira, Andre F. Correra, Thiago C. Cunha, Rodrigo L. O. R. Comasseto, Joao V. [UNIFESP] |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Princival, Cleverson R. Archilha, Marcos V. L. R. Dos Santos, Alcindo A. Franco, Mauricio P. Braga, Ataualpa A. C. Rodrigues-Oliveira, Andre F. Correra, Thiago C. Cunha, Rodrigo L. O. R. Comasseto, Joao V. [UNIFESP] |
description |
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 H-1, C-13, and Te-125 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, [TeOCl3](-), which was also observed in the hydrolysis of TeCl4. 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. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 2019-08-19T11:49:53Z 2019-08-19T11:49:53Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1021/acsomega.7b00628 Acs Omega. Washington, v. 2, n. 8, p. 4431-4439, 2017. 10.1021/acsomega.7b00628 WOS000409924000040.pdf 2470-1343 http://repositorio.unifesp.br/handle/11600/51424 WOS:000409924000040 |
url |
http://dx.doi.org/10.1021/acsomega.7b00628 http://repositorio.unifesp.br/handle/11600/51424 |
identifier_str_mv |
Acs Omega. Washington, v. 2, n. 8, p. 4431-4439, 2017. 10.1021/acsomega.7b00628 WOS000409924000040.pdf 2470-1343 WOS:000409924000040 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
4431-4439 application/pdf |
dc.publisher.none.fl_str_mv |
Amer Chemical Soc |
publisher.none.fl_str_mv |
Amer Chemical Soc |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268280426201088 |