Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures

Detalhes bibliográficos
Autor(a) principal: Rodríguez-Infante, Covadonga
Data de Publicação: 2001
Outros Autores: Esteban, David, Avecilla, Fernando, Blas, Andrés de, Rodríguez-Blas, Teresa, Mahía, Jose, Macedo, Anjos L., Geraldes, Carlos F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/3887
https://doi.org/10.1016/S0020-1693(01)00425-X
Resumo: Copper(II) complexes with a series of bibracchial lariat ethers are described. Independently of the nature of the counterion present (nitrate or perchlorate), the lariat ether N,N'-bis(2-aminobenzyl)-1,10-diaza-15-crown-5 (L1) always forms mononuclear complexes, whereas the lariat ethers N,N'-bis(2-aminobenzyl)-4,13-diaza-18-crown-6 (L2) and N,N'-bis(2-salicylaldiminobenzyl)-4,13-diaza-18-crown-6 (L3) only give binuclear compounds. The X-ray crystal structure of [CuL1](ClO4)2 shows a seven-coordinated copper(II) ion in a distorted (axially compressed) pentagonal-bipyramidal geometry. The X-ray crystal structure of [Cu2(L3-2H)](ClO4)2 confirms the binuclear nature of the compound with both metal ions having identical coordination environments and each one placed out of the crown hole but efficiently encapsulated by the corresponding pendant arm; each copper(II) ion is five-coordinated with an intermediate geometry between trigonal-bipyramidal and square-pyramidal ([tau]=0.40). The EPR spectra in frozen solution samples are in accordance with a stable coordinate pattern for the metal centre of ligand L1, yielding a rhombic distorted complex with axial compression in solution, in agreement with the X-ray crystal structure of [CuL1](ClO4)2. For the binuclear complexes of L2 and L3, the Cu(II) centres in solution can be distorted from their tetragonally elongated structures via interaction with ethanol and/or the nitrate counterion, leading to more than one species.
id RCAP_6963736f635c211bf038c34d9e92d323
oai_identifier_str oai:estudogeral.uc.pt:10316/3887
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Copper complexes with bibracchial lariat ethers: from mono- to binuclear structuresCopper(II) complexesMacrocycleLariat etherCrystal structuresEPR spectroscopyCopper(II) complexes with a series of bibracchial lariat ethers are described. Independently of the nature of the counterion present (nitrate or perchlorate), the lariat ether N,N'-bis(2-aminobenzyl)-1,10-diaza-15-crown-5 (L1) always forms mononuclear complexes, whereas the lariat ethers N,N'-bis(2-aminobenzyl)-4,13-diaza-18-crown-6 (L2) and N,N'-bis(2-salicylaldiminobenzyl)-4,13-diaza-18-crown-6 (L3) only give binuclear compounds. The X-ray crystal structure of [CuL1](ClO4)2 shows a seven-coordinated copper(II) ion in a distorted (axially compressed) pentagonal-bipyramidal geometry. The X-ray crystal structure of [Cu2(L3-2H)](ClO4)2 confirms the binuclear nature of the compound with both metal ions having identical coordination environments and each one placed out of the crown hole but efficiently encapsulated by the corresponding pendant arm; each copper(II) ion is five-coordinated with an intermediate geometry between trigonal-bipyramidal and square-pyramidal ([tau]=0.40). The EPR spectra in frozen solution samples are in accordance with a stable coordinate pattern for the metal centre of ligand L1, yielding a rhombic distorted complex with axial compression in solution, in agreement with the X-ray crystal structure of [CuL1](ClO4)2. For the binuclear complexes of L2 and L3, the Cu(II) centres in solution can be distorted from their tetragonally elongated structures via interaction with ethanol and/or the nitrate counterion, leading to more than one species.http://www.sciencedirect.com/science/article/B6TG5-433PCM9-T/1/7815e8fe94b2b6b2129e76252c3517d02001info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/3887http://hdl.handle.net/10316/3887https://doi.org/10.1016/S0020-1693(01)00425-XengInorganica Chimica Acta. 317:1-2 (2001) 190-198Rodríguez-Infante, CovadongaEsteban, DavidAvecilla, FernandoBlas, Andrés deRodríguez-Blas, TeresaMahía, JoseMacedo, Anjos L.Geraldes, Carlos F.info: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:RCAAP2021-09-01T09:05:29Zoai:estudogeral.uc.pt:10316/3887Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:47.151091Repositório 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 Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
title Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
spellingShingle Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
Rodríguez-Infante, Covadonga
Copper(II) complexes
Macrocycle
Lariat ether
Crystal structures
EPR spectroscopy
title_short Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
title_full Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
title_fullStr Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
title_full_unstemmed Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
title_sort Copper complexes with bibracchial lariat ethers: from mono- to binuclear structures
author Rodríguez-Infante, Covadonga
author_facet Rodríguez-Infante, Covadonga
Esteban, David
Avecilla, Fernando
Blas, Andrés de
Rodríguez-Blas, Teresa
Mahía, Jose
Macedo, Anjos L.
Geraldes, Carlos F.
author_role author
author2 Esteban, David
Avecilla, Fernando
Blas, Andrés de
Rodríguez-Blas, Teresa
Mahía, Jose
Macedo, Anjos L.
Geraldes, Carlos F.
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Rodríguez-Infante, Covadonga
Esteban, David
Avecilla, Fernando
Blas, Andrés de
Rodríguez-Blas, Teresa
Mahía, Jose
Macedo, Anjos L.
Geraldes, Carlos F.
dc.subject.por.fl_str_mv Copper(II) complexes
Macrocycle
Lariat ether
Crystal structures
EPR spectroscopy
topic Copper(II) complexes
Macrocycle
Lariat ether
Crystal structures
EPR spectroscopy
description Copper(II) complexes with a series of bibracchial lariat ethers are described. Independently of the nature of the counterion present (nitrate or perchlorate), the lariat ether N,N'-bis(2-aminobenzyl)-1,10-diaza-15-crown-5 (L1) always forms mononuclear complexes, whereas the lariat ethers N,N'-bis(2-aminobenzyl)-4,13-diaza-18-crown-6 (L2) and N,N'-bis(2-salicylaldiminobenzyl)-4,13-diaza-18-crown-6 (L3) only give binuclear compounds. The X-ray crystal structure of [CuL1](ClO4)2 shows a seven-coordinated copper(II) ion in a distorted (axially compressed) pentagonal-bipyramidal geometry. The X-ray crystal structure of [Cu2(L3-2H)](ClO4)2 confirms the binuclear nature of the compound with both metal ions having identical coordination environments and each one placed out of the crown hole but efficiently encapsulated by the corresponding pendant arm; each copper(II) ion is five-coordinated with an intermediate geometry between trigonal-bipyramidal and square-pyramidal ([tau]=0.40). The EPR spectra in frozen solution samples are in accordance with a stable coordinate pattern for the metal centre of ligand L1, yielding a rhombic distorted complex with axial compression in solution, in agreement with the X-ray crystal structure of [CuL1](ClO4)2. For the binuclear complexes of L2 and L3, the Cu(II) centres in solution can be distorted from their tetragonally elongated structures via interaction with ethanol and/or the nitrate counterion, leading to more than one species.
publishDate 2001
dc.date.none.fl_str_mv 2001
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/10316/3887
http://hdl.handle.net/10316/3887
https://doi.org/10.1016/S0020-1693(01)00425-X
url http://hdl.handle.net/10316/3887
https://doi.org/10.1016/S0020-1693(01)00425-X
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Inorganica Chimica Acta. 317:1-2 (2001) 190-198
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv aplication/PDF
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
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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
repository.mail.fl_str_mv
_version_ 1799133844232732672