Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes

Detalhes bibliográficos
Autor(a) principal: Arroyo, Marta
Data de Publicação: 2014
Outros Autores: Gomez-Iglesias, Patricia, Anton, Noelia, Garcia-Rodriguez, Raul, Alegria, Elisabete, Pombeiro, Armando, Miguel, Daniel, Villafane, Fernando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.21/4943
Resumo: fac-[MBr(CO)(3)(pypzH)] (M = Mn, Re; pypzH = (3-(2-pyridyl) pyrazole) complexes are prepared from fac[ MBr(CO)(3)(NCMe)(2)] and pypzH. The result of their deprotonation depends on the metallic substrate: the rhenium complex affords cleanly the bimetallic compound [fac-{Re(CO)(3)(mu(2)-pypz)}] 2 (mu(2)-pypz = mu(2)-3-(2pyridyl-. 1N) pyrazolate-2. 1N), which was crystallographically characterized, whereas a similar manganese complex was not detected. When two equivalents of pyridylpyrazolate are used, polymetallic species [fac-M(CO) 3(mu(2)-pypz)(mu(3)-pypz) M'] (mu(3)-pypz = mu(3)-3-(2-pyridyl-kappa N-1) pyrazolate-1 kappa 2N, N: 2. 1N:; M = Mn, M' = Li, Na, K; M = Re, M' = Na) are obtained. The crystal structures of the manganese carbonylate complexes were determined. The lithium complex is a monomer containing one manganese and one lithium atom, whereas the sodium and potassium complexes are dimers and reveal an unprecedented coordination mode for the bridging 3-(2-pyridyl) pyrazolate ligand, where the nitrogen of the pyridyl fragment and the nitrogen-1 of pyrazolate are chelated to manganese atoms, and each nitrogen-2 of pyrazolate is coordinated to two alkaline atoms. The polymetallic carbonylate complexes are unstable in solution and evolve spontaneously to [fac-{Re(CO) 3(mu(2)-pypz)}](2) or to the trimetallic paramagnetic species [MnII(mu(2)-pypz) 2{fac-{MnI(CO) 3(mu(2)-pypz)}(2)}]. The related complex cis-[MnCl2(pypzH)(2)] was also synthesized and structurally characterized. The electrochemical behavior of the new homo-and heteropolymetallic 3-(2-pyridyl) pyrazolate complexes has been studied and details of their redox properties are reported.
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spelling Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexesTricarbonylrhenium(I) bromide complexesCoordination compoundsCrystal structureX-rayMolecular structureElectrochemical parametrizationSpectroscopic propertiesAsymmetric catalysisPyrazole complexesRu(II) complexesfac-[MBr(CO)(3)(pypzH)] (M = Mn, Re; pypzH = (3-(2-pyridyl) pyrazole) complexes are prepared from fac[ MBr(CO)(3)(NCMe)(2)] and pypzH. The result of their deprotonation depends on the metallic substrate: the rhenium complex affords cleanly the bimetallic compound [fac-{Re(CO)(3)(mu(2)-pypz)}] 2 (mu(2)-pypz = mu(2)-3-(2pyridyl-. 1N) pyrazolate-2. 1N), which was crystallographically characterized, whereas a similar manganese complex was not detected. When two equivalents of pyridylpyrazolate are used, polymetallic species [fac-M(CO) 3(mu(2)-pypz)(mu(3)-pypz) M'] (mu(3)-pypz = mu(3)-3-(2-pyridyl-kappa N-1) pyrazolate-1 kappa 2N, N: 2. 1N:; M = Mn, M' = Li, Na, K; M = Re, M' = Na) are obtained. The crystal structures of the manganese carbonylate complexes were determined. The lithium complex is a monomer containing one manganese and one lithium atom, whereas the sodium and potassium complexes are dimers and reveal an unprecedented coordination mode for the bridging 3-(2-pyridyl) pyrazolate ligand, where the nitrogen of the pyridyl fragment and the nitrogen-1 of pyrazolate are chelated to manganese atoms, and each nitrogen-2 of pyrazolate is coordinated to two alkaline atoms. The polymetallic carbonylate complexes are unstable in solution and evolve spontaneously to [fac-{Re(CO) 3(mu(2)-pypz)}](2) or to the trimetallic paramagnetic species [MnII(mu(2)-pypz) 2{fac-{MnI(CO) 3(mu(2)-pypz)}(2)}]. The related complex cis-[MnCl2(pypzH)(2)] was also synthesized and structurally characterized. The electrochemical behavior of the new homo-and heteropolymetallic 3-(2-pyridyl) pyrazolate complexes has been studied and details of their redox properties are reported.Royal Society of ChemistryRCIPLArroyo, MartaGomez-Iglesias, PatriciaAnton, NoeliaGarcia-Rodriguez, RaulAlegria, ElisabetePombeiro, ArmandoMiguel, DanielVillafane, Fernando2015-08-24T11:30:12Z20142014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.21/4943engARROYO, Marta; [et al] – Homo-And Heteropolymetallic 3-(2-Pyridyl)Pyrazolate Manganese and Rhenium complexes. Dalton Transactions. ISSN: 1477-9226. Vol. 43, nr. 10 (2104), pp. 4009-40201477-922610.1039/c3dt53439ametadata only accessinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-08-03T09:47:41Zoai:repositorio.ipl.pt:10400.21/4943Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:14:18.112551Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
title Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
spellingShingle Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
Arroyo, Marta
Tricarbonylrhenium(I) bromide complexes
Coordination compounds
Crystal structure
X-ray
Molecular structure
Electrochemical parametrization
Spectroscopic properties
Asymmetric catalysis
Pyrazole complexes
Ru(II) complexes
title_short Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
title_full Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
title_fullStr Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
title_full_unstemmed Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
title_sort Homo-and heteropolymetallic 3-(2-pyridyl)pyrazolate manganese and rhenium complexes
author Arroyo, Marta
author_facet Arroyo, Marta
Gomez-Iglesias, Patricia
Anton, Noelia
Garcia-Rodriguez, Raul
Alegria, Elisabete
Pombeiro, Armando
Miguel, Daniel
Villafane, Fernando
author_role author
author2 Gomez-Iglesias, Patricia
Anton, Noelia
Garcia-Rodriguez, Raul
Alegria, Elisabete
Pombeiro, Armando
Miguel, Daniel
Villafane, Fernando
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv RCIPL
dc.contributor.author.fl_str_mv Arroyo, Marta
Gomez-Iglesias, Patricia
Anton, Noelia
Garcia-Rodriguez, Raul
Alegria, Elisabete
Pombeiro, Armando
Miguel, Daniel
Villafane, Fernando
dc.subject.por.fl_str_mv Tricarbonylrhenium(I) bromide complexes
Coordination compounds
Crystal structure
X-ray
Molecular structure
Electrochemical parametrization
Spectroscopic properties
Asymmetric catalysis
Pyrazole complexes
Ru(II) complexes
topic Tricarbonylrhenium(I) bromide complexes
Coordination compounds
Crystal structure
X-ray
Molecular structure
Electrochemical parametrization
Spectroscopic properties
Asymmetric catalysis
Pyrazole complexes
Ru(II) complexes
description fac-[MBr(CO)(3)(pypzH)] (M = Mn, Re; pypzH = (3-(2-pyridyl) pyrazole) complexes are prepared from fac[ MBr(CO)(3)(NCMe)(2)] and pypzH. The result of their deprotonation depends on the metallic substrate: the rhenium complex affords cleanly the bimetallic compound [fac-{Re(CO)(3)(mu(2)-pypz)}] 2 (mu(2)-pypz = mu(2)-3-(2pyridyl-. 1N) pyrazolate-2. 1N), which was crystallographically characterized, whereas a similar manganese complex was not detected. When two equivalents of pyridylpyrazolate are used, polymetallic species [fac-M(CO) 3(mu(2)-pypz)(mu(3)-pypz) M'] (mu(3)-pypz = mu(3)-3-(2-pyridyl-kappa N-1) pyrazolate-1 kappa 2N, N: 2. 1N:; M = Mn, M' = Li, Na, K; M = Re, M' = Na) are obtained. The crystal structures of the manganese carbonylate complexes were determined. The lithium complex is a monomer containing one manganese and one lithium atom, whereas the sodium and potassium complexes are dimers and reveal an unprecedented coordination mode for the bridging 3-(2-pyridyl) pyrazolate ligand, where the nitrogen of the pyridyl fragment and the nitrogen-1 of pyrazolate are chelated to manganese atoms, and each nitrogen-2 of pyrazolate is coordinated to two alkaline atoms. The polymetallic carbonylate complexes are unstable in solution and evolve spontaneously to [fac-{Re(CO) 3(mu(2)-pypz)}](2) or to the trimetallic paramagnetic species [MnII(mu(2)-pypz) 2{fac-{MnI(CO) 3(mu(2)-pypz)}(2)}]. The related complex cis-[MnCl2(pypzH)(2)] was also synthesized and structurally characterized. The electrochemical behavior of the new homo-and heteropolymetallic 3-(2-pyridyl) pyrazolate complexes has been studied and details of their redox properties are reported.
publishDate 2014
dc.date.none.fl_str_mv 2014
2014-01-01T00:00:00Z
2015-08-24T11:30:12Z
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://hdl.handle.net/10400.21/4943
url http://hdl.handle.net/10400.21/4943
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv ARROYO, Marta; [et al] – Homo-And Heteropolymetallic 3-(2-Pyridyl)Pyrazolate Manganese and Rhenium complexes. Dalton Transactions. ISSN: 1477-9226. Vol. 43, nr. 10 (2104), pp. 4009-4020
1477-9226
10.1039/c3dt53439a
dc.rights.driver.fl_str_mv metadata only access
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rights_invalid_str_mv metadata only access
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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