Publicação: Synthesis and antimycobacterial activity of new pyrazolate-bridged dinuclear complexes of the type [Pd(mu-L)(N-3)(PPh3)](2) (PPh3 = triphenylphosphine; L = pyrazolates)
dc.contributor.author | Silva, C. da [UNESP] | |
dc.contributor.author | Ferreira, J. G. [UNESP] | |
dc.contributor.author | Mauro, A. E. [UNESP] | |
dc.contributor.author | Frem, R. C. G. [UNESP] | |
dc.contributor.author | Santos, R. H. A. | |
dc.contributor.author | Silva, P. B. da [UNESP] | |
dc.contributor.author | Pavan, Fernando Rogério [UNESP] | |
dc.contributor.author | Marino, L. B. [UNESP] | |
dc.contributor.author | Leite, Clarice Queico Fujimura [UNESP] | |
dc.contributor.author | Netto, A. V. G. [UNESP] | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2015-03-18T15:53:33Z | |
dc.date.available | 2015-03-18T15:53:33Z | |
dc.date.issued | 2014-10-01 | |
dc.description.abstract | Binuclear compounds of the type [Pd(mu-L)(N-3)(PPh3)](2) {L = pyrazolate (1); 3,5-dimethylpyrazolate (2); 4-iodopyrazolate (3); PPh3 = triphenylphosphine} were synthesized and characterized by elemental analyses, infrared and H-1 and P-31{H-1} NMR spectroscopies. The crystal and molecular structures of the complex [Pd(mu-dmPz)(N-3)(PPh3)](2) (2) were determined by single-crystal X-ray diffraction techniques. In vitro antimycobacterial evaluation demonstrated that compound [Pd(mu-Pz)(N-3)(PPh3)](2) (1) displayed a MIC of 8.16 mu M, being more active than some commonly used anti-TB drugs and other Pd(II) complexes. (C) 2014 Elsevier B.V. All rights reserved. | en |
dc.description.affiliation | Univ Estadual Paulista, Inst Quim Araraquara, Araraquara, SP, Brazil | |
dc.description.affiliation | Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil | |
dc.description.affiliation | Univ Estadual Paulista, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil | |
dc.description.affiliationUnesp | Univ Estadual Paulista, Inst Quim Araraquara, Araraquara, SP, Brazil | |
dc.description.affiliationUnesp | Univ Estadual Paulista, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description.sponsorshipId | FAPESP: 12/15486-3 | |
dc.description.sponsorshipId | CNPq: 475322/2009-6 | |
dc.description.sponsorshipId | CNPq: 487092/2012-0 | |
dc.format.extent | 153-155 | |
dc.identifier | http://dx.doi.org/10.1016/j.inoche.2014.09.001 | |
dc.identifier.citation | Inorganic Chemistry Communications. Amsterdam: Elsevier Science Bv, v. 48, p. 153-155, 2014. | |
dc.identifier.doi | 10.1016/j.inoche.2014.09.001 | |
dc.identifier.issn | 1387-7003 | |
dc.identifier.lattes | 2114570774349859 | |
dc.identifier.lattes | 7927677053650819 | |
dc.identifier.lattes | 8534138813417161 | |
dc.identifier.orcid | 0000-0002-0057-7964 | |
dc.identifier.orcid | 0000-0003-1574-681X | |
dc.identifier.uri | http://hdl.handle.net/11449/116580 | |
dc.identifier.wos | WOS:000343362500036 | |
dc.language.iso | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation.ispartof | Inorganic Chemistry Communications | |
dc.relation.ispartofjcr | 1.810 | |
dc.relation.ispartofsjr | 0,430 | |
dc.rights.accessRights | Acesso restrito | pt |
dc.source | Web of Science | |
dc.subject | Binuclear Pd(II) compounds | en |
dc.subject | Triphenylphosphine | en |
dc.subject | Pyrazolates | en |
dc.subject | Mycobacterium tuberculosis | en |
dc.title | Synthesis and antimycobacterial activity of new pyrazolate-bridged dinuclear complexes of the type [Pd(mu-L)(N-3)(PPh3)](2) (PPh3 = triphenylphosphine; L = pyrazolates) | en |
dc.type | Artigo | pt |
dcterms.license | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dcterms.rightsHolder | Elsevier B.V. | |
dspace.entity.type | Publication | |
relation.isDepartmentOfPublication | 5004bcab-94af-4939-b980-091ae9d0a19e | |
relation.isDepartmentOfPublication.latestForDiscovery | 5004bcab-94af-4939-b980-091ae9d0a19e | |
relation.isOrgUnitOfPublication | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
relation.isOrgUnitOfPublication.latestForDiscovery | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
unesp.author.lattes | 2114570774349859 | |
unesp.author.lattes | 7927677053650819[10] | |
unesp.author.lattes | 3300223970814448[3] | |
unesp.author.lattes | 8534138813417161[4] | |
unesp.author.orcid | 0000-0002-0057-7964[10] | |
unesp.author.orcid | 0000-0002-6969-3963[7] | |
unesp.author.orcid | 0000-0003-0047-4671[3] | |
unesp.author.orcid | 0000-0003-1574-681X[4] | |
unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara | pt |
unesp.department | Ciências Biológicas - FCF | pt |