Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior

Detalhes bibliográficos
Autor(a) principal: Hurtado,John
Data de Publicação: 2011
Outros Autores: Ibañez,Andrés, Rojas,René, Valderrama,Mauricio, Fröhlich,Roland
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=S0103-50532011000900018
Resumo: The reaction of 2-bromo-1, 3-bis(bromomethyl)benzene with 3, 5-dimethylpyrazole and 1H-indazole yields the tridentate ligands 2-bromo-1, 3-bis(3, 5-dimethylpirazol-1-ylmethyl)benzene (1) and 2-bromo-1, 3-bis(indazol-2-ylmethyl)benzene (2). These compounds react with [Ni(cod)2] in tetrahydrofuran (thf) to form the oxidative addition complexes [NiBr{1, 3-bis(azolylmethyl)phenyl-N, C, N}], azol = 3, 5-dimethylpyrazol (3), indazol (4), which were isolated in good yields as stable yellow solids and characterized by elemental analysis, Fourier-transform infrared spectroscopy (FTIR), mass spectroscopy and nuclear magnetic resonance (NMR). In addition, the molecular structures of 2 and 4 were determined by single-crystal X-ray diffraction analysis. Complex 4 was tested as a catalyst in ethylene polymerization reaction
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spelling Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behaviornickeltridentate ligandscyclometalated complexescatalytic activityThe reaction of 2-bromo-1, 3-bis(bromomethyl)benzene with 3, 5-dimethylpyrazole and 1H-indazole yields the tridentate ligands 2-bromo-1, 3-bis(3, 5-dimethylpirazol-1-ylmethyl)benzene (1) and 2-bromo-1, 3-bis(indazol-2-ylmethyl)benzene (2). These compounds react with [Ni(cod)2] in tetrahydrofuran (thf) to form the oxidative addition complexes [NiBr{1, 3-bis(azolylmethyl)phenyl-N, C, N}], azol = 3, 5-dimethylpyrazol (3), indazol (4), which were isolated in good yields as stable yellow solids and characterized by elemental analysis, Fourier-transform infrared spectroscopy (FTIR), mass spectroscopy and nuclear magnetic resonance (NMR). In addition, the molecular structures of 2 and 4 were determined by single-crystal X-ray diffraction analysis. Complex 4 was tested as a catalyst in ethylene polymerization reactionSociedade Brasileira de Química2011-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000900018Journal of the Brazilian Chemical Society v.22 n.9 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011000900018info:eu-repo/semantics/openAccessHurtado,JohnIbañez,AndrésRojas,RenéValderrama,MauricioFröhlich,Rolandeng2011-09-20T00:00:00Zoai:scielo:S0103-50532011000900018Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-09-20T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
title Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
spellingShingle Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
Hurtado,John
nickel
tridentate ligands
cyclometalated complexes
catalytic activity
title_short Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
title_full Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
title_fullStr Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
title_full_unstemmed Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
title_sort Organonickel(II) complexes with anionic tridentate 1, 3-bis(azolylmethyl)phenyl ligands. synthesis, structural characterization and catalytic behavior
author Hurtado,John
author_facet Hurtado,John
Ibañez,Andrés
Rojas,René
Valderrama,Mauricio
Fröhlich,Roland
author_role author
author2 Ibañez,Andrés
Rojas,René
Valderrama,Mauricio
Fröhlich,Roland
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Hurtado,John
Ibañez,Andrés
Rojas,René
Valderrama,Mauricio
Fröhlich,Roland
dc.subject.por.fl_str_mv nickel
tridentate ligands
cyclometalated complexes
catalytic activity
topic nickel
tridentate ligands
cyclometalated complexes
catalytic activity
description The reaction of 2-bromo-1, 3-bis(bromomethyl)benzene with 3, 5-dimethylpyrazole and 1H-indazole yields the tridentate ligands 2-bromo-1, 3-bis(3, 5-dimethylpirazol-1-ylmethyl)benzene (1) and 2-bromo-1, 3-bis(indazol-2-ylmethyl)benzene (2). These compounds react with [Ni(cod)2] in tetrahydrofuran (thf) to form the oxidative addition complexes [NiBr{1, 3-bis(azolylmethyl)phenyl-N, C, N}], azol = 3, 5-dimethylpyrazol (3), indazol (4), which were isolated in good yields as stable yellow solids and characterized by elemental analysis, Fourier-transform infrared spectroscopy (FTIR), mass spectroscopy and nuclear magnetic resonance (NMR). In addition, the molecular structures of 2 and 4 were determined by single-crystal X-ray diffraction analysis. Complex 4 was tested as a catalyst in ethylene polymerization reaction
publishDate 2011
dc.date.none.fl_str_mv 2011-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000900018
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000900018
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532011000900018
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.22 n.9 2011
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
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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)
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