Síntese e caracterização de complexos metálicos de antimônio, bismuto e estanho com lapachol

Detalhes bibliográficos
Ano de defesa: 2009
Autor(a) principal: Meiriane Mariano da Silva
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Minas Gerais
Brasil
ICX - DEPARTAMENTO DE QUÍMICA
Programa de Pós-Graduação em Química
UFMG
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://hdl.handle.net/1843/48458
Resumo: Lapachol is a natural naphthoquinone with broad spectrum of biological activities, including antitumor, antileishmania, antiviral, analgesic, antifungal properties. Because of its antitumor property, changes in the structure of lapachol have been made such as to reduce its side effects without affecting its effectiveness. One option is to use the lapachol as ligand in coordination compounds. The lapachol was found to form 1:1 complexes with antimony(V), bismuth(V) and tin(IV), hypothesis confirmed by elemental analysis. Characterization of the complexes by infrared and ¹H and ¹³C NMR spectroscopies revealed that the coordination occurs through the formation of a chelate ring with the lapachol keto-enol oxygens. UV-Vis absoption, molar conductivity, thermogravimetry and mass spectrometry with electrospray ionization were also used to characterize the complexes. The three compounds synthesized, when added to a medium containing leukemia tumor cells, inhibited the cell growth, indicating an antitumor activity against this cell type. The complexation of lapachol to bismuth produced a compound about 2.4 times as effective as non-complexed lapachol. On the other hand, Sb- and Sn-lapachol complexes exhibited similar activities when compared to the metal salts used in the synthesis and no improvement was observed when compared to lapachol.