Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols

Detalhes bibliográficos
Autor(a) principal: Ma, Zhen
Data de Publicação: 2014
Outros Autores: Wei, Lijuan, Alegria, Elisabete, Martins, Luisa, Guedes Da Silva, M. Fátima C., Pombeiro, Armando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.21/4958
Resumo: The reactions between 4'-phenyl-terpyridine (L) and nitrate, acetate or chloride Cu(II) salts led to the formation of [Cu(NO3)(2)L] (1), [Cu(OCOCH3)(2)L]center dot CH2Cl2 (2 center dot CH2Cl2)and [CuCl2L]center dot[Cu(Cl)(mu-Cl)L](2) (3), respectively. Upon dissolving 1 in mixtures of DMSO-MeOH or EtOH-DMF the compounds [Cu(H2O){OS(CH3)(2)}L]-(NO3)(2) (4) and [Cu(HO)(CH3CH2OH)L](NO3) (5) were obtained, in this order. Reaction of 3 with AgSO3CF3 led to [CuCl(OSO2CF3)L] (6). The compounds were characterized by ESI-MS, IR, elemental analysis, electrochemical techniques and, for 2-6, also by single crystal X-ray diffraction. They undergo, by cyclic voltammetry, two single-electron irreversible reductions assigned to Cu(II) -> Cu(I)and Cu(I) -> Cu(0) and, for those of the same structural type, the reduction potential appears to correlate with the summation of the values of the Lever electrochemical EL ligand parameter, which is reported for the first time for copper complexes. Complexes 1-6 in combination with TEMPO (2,2,6,6-tetramethylpiperidinyl-1-oxyl radical) can exhibit a high catalytic activity, under mild conditions and in alkaline aqueous solution, for the aerobic oxidation of benzylic alcohols. Molar yields up to 94% (based on the alcohol) with TON values up to 320 were achieved after 22 h.
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spelling Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcoholsSolid-state photoluminescenceCoordination-compoundsMild conditionsSilver(I)-2,2'/6',2''-terpyridine complexesElectrochemical parametrizationCarboxyphenyl-terpyridineCorresponding aldehydesMolecular-structureBuilding-blockLigandsThe reactions between 4'-phenyl-terpyridine (L) and nitrate, acetate or chloride Cu(II) salts led to the formation of [Cu(NO3)(2)L] (1), [Cu(OCOCH3)(2)L]center dot CH2Cl2 (2 center dot CH2Cl2)and [CuCl2L]center dot[Cu(Cl)(mu-Cl)L](2) (3), respectively. Upon dissolving 1 in mixtures of DMSO-MeOH or EtOH-DMF the compounds [Cu(H2O){OS(CH3)(2)}L]-(NO3)(2) (4) and [Cu(HO)(CH3CH2OH)L](NO3) (5) were obtained, in this order. Reaction of 3 with AgSO3CF3 led to [CuCl(OSO2CF3)L] (6). The compounds were characterized by ESI-MS, IR, elemental analysis, electrochemical techniques and, for 2-6, also by single crystal X-ray diffraction. They undergo, by cyclic voltammetry, two single-electron irreversible reductions assigned to Cu(II) -> Cu(I)and Cu(I) -> Cu(0) and, for those of the same structural type, the reduction potential appears to correlate with the summation of the values of the Lever electrochemical EL ligand parameter, which is reported for the first time for copper complexes. Complexes 1-6 in combination with TEMPO (2,2,6,6-tetramethylpiperidinyl-1-oxyl radical) can exhibit a high catalytic activity, under mild conditions and in alkaline aqueous solution, for the aerobic oxidation of benzylic alcohols. Molar yields up to 94% (based on the alcohol) with TON values up to 320 were achieved after 22 h.Royal Society of ChemistryRCIPLMa, ZhenWei, LijuanAlegria, ElisabeteMartins, LuisaGuedes Da Silva, M. Fátima C.Pombeiro, Armando2015-08-24T13:54:08Z20142014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.21/4958engMA, Zhen; [et al] – Synthesis and characterization of copper(II) 4´-Phenyl-Terpyridine compounds and catalytic application for aerobic oxidation of Benzylic Alcohols. Dalton Transactions. ISSN: 1477-9226. Vol. 43, nr. 10 (2014), pp. 4048-40581477-922610.1039/c3dt53054jmetadata 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:RCAAP2023-08-03T09:47:43Zoai:repositorio.ipl.pt:10400.21/4958Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:14:18.875888Repositório 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 Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
title Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
spellingShingle Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
Ma, Zhen
Solid-state photoluminescence
Coordination-compounds
Mild conditions
Silver(I)-2,2'/6',2''-terpyridine complexes
Electrochemical parametrization
Carboxyphenyl-terpyridine
Corresponding aldehydes
Molecular-structure
Building-block
Ligands
title_short Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
title_full Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
title_fullStr Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
title_full_unstemmed Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
title_sort Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
author Ma, Zhen
author_facet Ma, Zhen
Wei, Lijuan
Alegria, Elisabete
Martins, Luisa
Guedes Da Silva, M. Fátima C.
Pombeiro, Armando
author_role author
author2 Wei, Lijuan
Alegria, Elisabete
Martins, Luisa
Guedes Da Silva, M. Fátima C.
Pombeiro, Armando
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv RCIPL
dc.contributor.author.fl_str_mv Ma, Zhen
Wei, Lijuan
Alegria, Elisabete
Martins, Luisa
Guedes Da Silva, M. Fátima C.
Pombeiro, Armando
dc.subject.por.fl_str_mv Solid-state photoluminescence
Coordination-compounds
Mild conditions
Silver(I)-2,2'/6',2''-terpyridine complexes
Electrochemical parametrization
Carboxyphenyl-terpyridine
Corresponding aldehydes
Molecular-structure
Building-block
Ligands
topic Solid-state photoluminescence
Coordination-compounds
Mild conditions
Silver(I)-2,2'/6',2''-terpyridine complexes
Electrochemical parametrization
Carboxyphenyl-terpyridine
Corresponding aldehydes
Molecular-structure
Building-block
Ligands
description The reactions between 4'-phenyl-terpyridine (L) and nitrate, acetate or chloride Cu(II) salts led to the formation of [Cu(NO3)(2)L] (1), [Cu(OCOCH3)(2)L]center dot CH2Cl2 (2 center dot CH2Cl2)and [CuCl2L]center dot[Cu(Cl)(mu-Cl)L](2) (3), respectively. Upon dissolving 1 in mixtures of DMSO-MeOH or EtOH-DMF the compounds [Cu(H2O){OS(CH3)(2)}L]-(NO3)(2) (4) and [Cu(HO)(CH3CH2OH)L](NO3) (5) were obtained, in this order. Reaction of 3 with AgSO3CF3 led to [CuCl(OSO2CF3)L] (6). The compounds were characterized by ESI-MS, IR, elemental analysis, electrochemical techniques and, for 2-6, also by single crystal X-ray diffraction. They undergo, by cyclic voltammetry, two single-electron irreversible reductions assigned to Cu(II) -> Cu(I)and Cu(I) -> Cu(0) and, for those of the same structural type, the reduction potential appears to correlate with the summation of the values of the Lever electrochemical EL ligand parameter, which is reported for the first time for copper complexes. Complexes 1-6 in combination with TEMPO (2,2,6,6-tetramethylpiperidinyl-1-oxyl radical) can exhibit a high catalytic activity, under mild conditions and in alkaline aqueous solution, for the aerobic oxidation of benzylic alcohols. Molar yields up to 94% (based on the alcohol) with TON values up to 320 were achieved after 22 h.
publishDate 2014
dc.date.none.fl_str_mv 2014
2014-01-01T00:00:00Z
2015-08-24T13:54:08Z
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/10400.21/4958
url http://hdl.handle.net/10400.21/4958
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv MA, Zhen; [et al] – Synthesis and characterization of copper(II) 4´-Phenyl-Terpyridine compounds and catalytic application for aerobic oxidation of Benzylic Alcohols. Dalton Transactions. ISSN: 1477-9226. Vol. 43, nr. 10 (2014), pp. 4048-4058
1477-9226
10.1039/c3dt53054j
dc.rights.driver.fl_str_mv metadata only access
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eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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