SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS

Detalhes bibliográficos
Autor(a) principal: Thomazella, Nathalia A. [UNESP]
Data de Publicação: 2018
Outros Autores: Lemos, Sahra C. [UNESP], Souza, Ronan F. F. de [UNESP], Souza, Rodrigo A. de [UNESP], Mauro, Antonio E. [UNESP], Carlos, Iracilda Z. [UNESP], Netto, Adelino V. G. [UNESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.21577/0100-4042.20170293
http://hdl.handle.net/11449/185128
Resumo: The halide bridge cleavage reaction of the [Pd(C-2,N-bzox)(mu-Cl)](2). compound (bzox = benzaldehydeoxime) with ethylenethiourea (L) in the 1:2 molar ratio at room temperature yielded the cyclopalladated compound [Pd(C-2,N-bzox)(Cl)(L)] (1) whose replacement of the halide group by the addition of suitable salts afforded compounds of general formulae [Pd((C-2,N-bzox)(X)(L)] = {X = Br- (2), I-(3)}. All compounds were characterized by melting point, elemental analyses, infrared and H-1- and C-13{H-1}-NMR spectroscopies revealing the complexes formation with the oxime coordinated to Pd(II) as C,N-chelating and the ethylenethiourea as a monodentate ligand via the sulfur atom. Hie cytotoxicity of cyclopalladated compounds has been evaluated in vitro against murine mammary tumor cell (LM3) showing cytotoxic activity similar to cisplatin.
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spelling SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDScyclopalladated complexesoximesethylenethioureaimidazolidine-2-thionecytotoxicityThe halide bridge cleavage reaction of the [Pd(C-2,N-bzox)(mu-Cl)](2). compound (bzox = benzaldehydeoxime) with ethylenethiourea (L) in the 1:2 molar ratio at room temperature yielded the cyclopalladated compound [Pd(C-2,N-bzox)(Cl)(L)] (1) whose replacement of the halide group by the addition of suitable salts afforded compounds of general formulae [Pd((C-2,N-bzox)(X)(L)] = {X = Br- (2), I-(3)}. All compounds were characterized by melting point, elemental analyses, infrared and H-1- and C-13{H-1}-NMR spectroscopies revealing the complexes formation with the oxime coordinated to Pd(II) as C,N-chelating and the ethylenethiourea as a monodentate ligand via the sulfur atom. Hie cytotoxicity of cyclopalladated compounds has been evaluated in vitro against murine mammary tumor cell (LM3) showing cytotoxic activity similar to cisplatin.Univ Estadual Paulista, Dept Quim Geral & Inorgan, Inst Quim, BR-14800060 Araraquara, SP, BrazilUniv Estadual Paulista, Dept Anal Clin, Fac Ciencias Farmaceut, BR-14800903 Araraquara, SP, BrazilUniv Estadual Paulista, Dept Quim Geral & Inorgan, Inst Quim, BR-14800060 Araraquara, SP, BrazilUniv Estadual Paulista, Dept Anal Clin, Fac Ciencias Farmaceut, BR-14800903 Araraquara, SP, BrazilSoc Brasileira QuimicaUniversidade Estadual Paulista (Unesp)Thomazella, Nathalia A. [UNESP]Lemos, Sahra C. [UNESP]Souza, Ronan F. F. de [UNESP]Souza, Rodrigo A. de [UNESP]Mauro, Antonio E. [UNESP]Carlos, Iracilda Z. [UNESP]Netto, Adelino V. G. [UNESP]2019-10-04T12:32:48Z2019-10-04T12:32:48Z2018-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1150-1155application/pdfhttp://dx.doi.org/10.21577/0100-4042.20170293Quimica Nova. Sao Paulo: Soc Brasileira Quimica, v. 41, n. 10, p. 1150-1155, 2018.0100-4042http://hdl.handle.net/11449/18512810.21577/0100-4042.20170293S0100-40422018001001150WOS:000451630400008S0100-40422018001001150.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporQuimica Novainfo:eu-repo/semantics/openAccess2024-06-21T15:19:09Zoai:repositorio.unesp.br:11449/185128Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:22:47.895918Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
title SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
spellingShingle SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
Thomazella, Nathalia A. [UNESP]
cyclopalladated complexes
oximes
ethylenethiourea
imidazolidine-2-thione
cytotoxicity
title_short SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
title_full SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
title_fullStr SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
title_full_unstemmed SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
title_sort SYNTHESIS; CHARACTERIZATION AND CYTOTOXIC ACTIVITY EVALUATION OF CYCLOPALLADATED COMPOUNDS CONTAINING ORTHOMETALLATED BENZALDEHYDEOXIME AND ETHYLENETHIOUREA AS LIGANDS
author Thomazella, Nathalia A. [UNESP]
author_facet Thomazella, Nathalia A. [UNESP]
Lemos, Sahra C. [UNESP]
Souza, Ronan F. F. de [UNESP]
Souza, Rodrigo A. de [UNESP]
Mauro, Antonio E. [UNESP]
Carlos, Iracilda Z. [UNESP]
Netto, Adelino V. G. [UNESP]
author_role author
author2 Lemos, Sahra C. [UNESP]
Souza, Ronan F. F. de [UNESP]
Souza, Rodrigo A. de [UNESP]
Mauro, Antonio E. [UNESP]
Carlos, Iracilda Z. [UNESP]
Netto, Adelino V. G. [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Thomazella, Nathalia A. [UNESP]
Lemos, Sahra C. [UNESP]
Souza, Ronan F. F. de [UNESP]
Souza, Rodrigo A. de [UNESP]
Mauro, Antonio E. [UNESP]
Carlos, Iracilda Z. [UNESP]
Netto, Adelino V. G. [UNESP]
dc.subject.por.fl_str_mv cyclopalladated complexes
oximes
ethylenethiourea
imidazolidine-2-thione
cytotoxicity
topic cyclopalladated complexes
oximes
ethylenethiourea
imidazolidine-2-thione
cytotoxicity
description The halide bridge cleavage reaction of the [Pd(C-2,N-bzox)(mu-Cl)](2). compound (bzox = benzaldehydeoxime) with ethylenethiourea (L) in the 1:2 molar ratio at room temperature yielded the cyclopalladated compound [Pd(C-2,N-bzox)(Cl)(L)] (1) whose replacement of the halide group by the addition of suitable salts afforded compounds of general formulae [Pd((C-2,N-bzox)(X)(L)] = {X = Br- (2), I-(3)}. All compounds were characterized by melting point, elemental analyses, infrared and H-1- and C-13{H-1}-NMR spectroscopies revealing the complexes formation with the oxime coordinated to Pd(II) as C,N-chelating and the ethylenethiourea as a monodentate ligand via the sulfur atom. Hie cytotoxicity of cyclopalladated compounds has been evaluated in vitro against murine mammary tumor cell (LM3) showing cytotoxic activity similar to cisplatin.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-01
2019-10-04T12:32:48Z
2019-10-04T12:32:48Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.21577/0100-4042.20170293
Quimica Nova. Sao Paulo: Soc Brasileira Quimica, v. 41, n. 10, p. 1150-1155, 2018.
0100-4042
http://hdl.handle.net/11449/185128
10.21577/0100-4042.20170293
S0100-40422018001001150
WOS:000451630400008
S0100-40422018001001150.pdf
url http://dx.doi.org/10.21577/0100-4042.20170293
http://hdl.handle.net/11449/185128
identifier_str_mv Quimica Nova. Sao Paulo: Soc Brasileira Quimica, v. 41, n. 10, p. 1150-1155, 2018.
0100-4042
10.21577/0100-4042.20170293
S0100-40422018001001150
WOS:000451630400008
S0100-40422018001001150.pdf
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Quimica Nova
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1150-1155
application/pdf
dc.publisher.none.fl_str_mv Soc Brasileira Quimica
publisher.none.fl_str_mv Soc Brasileira Quimica
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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