Synthesis and characterization of copper(II) 4´-phenyl-terpyridine compounds and catalytic application for aerobic oxidation of benzylic alcohols
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , |
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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7160 |
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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 info:eu-repo/semantics/openAccess |
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) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799133400584421376 |