Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine
Autor(a) principal: | |
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Data de Publicação: | 1997 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500017 |
Resumo: | A potentiometric and spectrophotometric study of physiologically interesting CuII mixed ligand complexes has been performed involving hydroxamic acids as primary ligands (A) and secondary ligands (B) represented either by histamine or the aminoacids glycine and histidine. All are potentially able to form chelate complexes with either five or six membered rings. The formation constant and the visible absorption spectrum were calculated for each one of the identified species, both binary and mixed ones. The most probable structures of the mixed species are discussed based upon their formation constants, their stabilization with regard to the two binary species as well as their visible absorption. It was evidenced that Cu-hydroxamate complexes do not favour significantly mixed ligand complex formation with aminoacids having only the carboxylate and amino groups; however, these complexes are strongly formed with histidine, due to the presence of the imidazol group. |
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Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidinehydroxamic acidcopper(II) complexesmixed ligand complexeshistidineglycineA potentiometric and spectrophotometric study of physiologically interesting CuII mixed ligand complexes has been performed involving hydroxamic acids as primary ligands (A) and secondary ligands (B) represented either by histamine or the aminoacids glycine and histidine. All are potentially able to form chelate complexes with either five or six membered rings. The formation constant and the visible absorption spectrum were calculated for each one of the identified species, both binary and mixed ones. The most probable structures of the mixed species are discussed based upon their formation constants, their stabilization with regard to the two binary species as well as their visible absorption. It was evidenced that Cu-hydroxamate complexes do not favour significantly mixed ligand complex formation with aminoacids having only the carboxylate and amino groups; however, these complexes are strongly formed with histidine, due to the presence of the imidazol group.Sociedade Brasileira de Química1997-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500017Journal of the Brazilian Chemical Society v.8 n.5 1997reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50531997000500017info:eu-repo/semantics/openAccessFernandes,Maria Celina M.M.Paniago,Eucler B.Carvalho,Sandraeng2010-09-10T00:00:00Zoai:scielo:S0103-50531997000500017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-09-10T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine |
title |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine |
spellingShingle |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine Fernandes,Maria Celina M.M. hydroxamic acid copper(II) complexes mixed ligand complexes histidine glycine |
title_short |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine |
title_full |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine |
title_fullStr |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine |
title_full_unstemmed |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine |
title_sort |
Copper(II) mixed ligands complexes of hydroxamic acids with glycine, histamine and histidine |
author |
Fernandes,Maria Celina M.M. |
author_facet |
Fernandes,Maria Celina M.M. Paniago,Eucler B. Carvalho,Sandra |
author_role |
author |
author2 |
Paniago,Eucler B. Carvalho,Sandra |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Fernandes,Maria Celina M.M. Paniago,Eucler B. Carvalho,Sandra |
dc.subject.por.fl_str_mv |
hydroxamic acid copper(II) complexes mixed ligand complexes histidine glycine |
topic |
hydroxamic acid copper(II) complexes mixed ligand complexes histidine glycine |
description |
A potentiometric and spectrophotometric study of physiologically interesting CuII mixed ligand complexes has been performed involving hydroxamic acids as primary ligands (A) and secondary ligands (B) represented either by histamine or the aminoacids glycine and histidine. All are potentially able to form chelate complexes with either five or six membered rings. The formation constant and the visible absorption spectrum were calculated for each one of the identified species, both binary and mixed ones. The most probable structures of the mixed species are discussed based upon their formation constants, their stabilization with regard to the two binary species as well as their visible absorption. It was evidenced that Cu-hydroxamate complexes do not favour significantly mixed ligand complex formation with aminoacids having only the carboxylate and amino groups; however, these complexes are strongly formed with histidine, due to the presence of the imidazol group. |
publishDate |
1997 |
dc.date.none.fl_str_mv |
1997-01-01 |
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500017 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50531997000500017 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.8 n.5 1997 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
_version_ |
1750318163079200768 |