Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes
Dinuclear lanthanide complexes [((HB(pz)3)2Dy)2(μ-Th2An)] (1Dy) and [((HB(pz)3)2Dy)2(μ-ClCNAn)] (2Dy), based on the hydrotris(pyrazol-1-yl)borate (HBpz3−) scorpionate capping ligand and anilate (An2−) bridging linkers, namely homosubstituted dithiophene- and heterosubstituted chlorocyanoanilate, bea...
| Autores: | , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2072/537606 |
| Acceso en línea: | http://hdl.handle.net/2072/537606 https://doi.org/10.1039/D4DT00175C |
| Access Level: | acceso abierto |
| Palabra clave: | Química 54 - Química |
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Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexesManna, FabioOggianu, MariangelaGalán-Mascarós, José RamónPop, FlaviaLe Guennic, BorisMercuri, Maria LauraAvarvari, NarcisQuímica54 - QuímicaDinuclear lanthanide complexes [((HB(pz)3)2Dy)2(μ-Th2An)] (1Dy) and [((HB(pz)3)2Dy)2(μ-ClCNAn)] (2Dy), based on the hydrotris(pyrazol-1-yl)borate (HBpz3−) scorpionate capping ligand and anilate (An2−) bridging linkers, namely homosubstituted dithiophene- and heterosubstituted chlorocyanoanilate, bearing electron-donating and withdrawing substituents at the 3,6-positions of the benzoquinone core, are reported. 1Dy shows an octacoordinated {N6O2} DyIII ion within a D4h distorted square antiprismatic coordination, an ideal geometry for Single-Molecule Magnet (SMM) behavior, given its oblate nature, whereas in 2Dy the octacoordinated DyIII ion adopts a D2d triangular dodecahedron geometry, while maintaining the same {N6O2} coordination sphere. Both complexes show field-induced single molecule magnet (SMM) behaviour, with tuning of the slow magnetic relaxation as a function of the nature of the substituents at the 3,6-positions of the anilate moiety. A comparison of the Arrhenius fitting parameters for 1Dy and 2Dy supports the hypothesis that square antiprismatic DyIII complexes, as 1Dy, exhibit higher energy barriers. This interpretation is supported by ab initio calculations that also shed light on the crucial role of intermolecular dipolar interactions.Royal Society of Chemistry2024info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersion25 p.application/pdfhttp://hdl.handle.net/2072/537606https://doi.org/10.1039/D4DT00175CRECERCAT (Dipòsit de la Recerca de Catalunya)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésFondazione di Sardegna, Convenzione Triennale tra la Fondazione di Sardegna e gli Atenei Sardi, Regione Sardegna, L.R. 7/2007 annualità 2020, through the SMAWRT project (CUP F75F21001260007)MCIN/AEI/10.13039/501100011033/ through project PID2021-124796OB-I00Generalitat de Catalunya (2021SGR1154)Ministerio de Ciencia e Innovación through the Severo Ochoa Excellence Accreditations CEX2019-000925-S (MCIN/AEI) and CEX2021-001214-SCERCA Programme/Generalitat de CatalunyaCC-BYinfo:eu-repo/semantics/openAccessoai:recercat.cat:2072/5376062026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes |
| title |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes |
| spellingShingle |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes Manna, Fabio Química 54 - Química |
| title_short |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes |
| title_full |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes |
| title_fullStr |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes |
| title_full_unstemmed |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes |
| title_sort |
Tuning the slow magnetic relaxation with the substituents in anilate bridged bis(dysprosium) complexes |
| dc.creator.none.fl_str_mv |
Manna, Fabio Oggianu, Mariangela Galán-Mascarós, José Ramón Pop, Flavia Le Guennic, Boris Mercuri, Maria Laura Avarvari, Narcis |
| author |
Manna, Fabio |
| author_facet |
Manna, Fabio Oggianu, Mariangela Galán-Mascarós, José Ramón Pop, Flavia Le Guennic, Boris Mercuri, Maria Laura Avarvari, Narcis |
| author_role |
author |
| author2 |
Oggianu, Mariangela Galán-Mascarós, José Ramón Pop, Flavia Le Guennic, Boris Mercuri, Maria Laura Avarvari, Narcis |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Química 54 - Química |
| topic |
Química 54 - Química |
| description |
Dinuclear lanthanide complexes [((HB(pz)3)2Dy)2(μ-Th2An)] (1Dy) and [((HB(pz)3)2Dy)2(μ-ClCNAn)] (2Dy), based on the hydrotris(pyrazol-1-yl)borate (HBpz3−) scorpionate capping ligand and anilate (An2−) bridging linkers, namely homosubstituted dithiophene- and heterosubstituted chlorocyanoanilate, bearing electron-donating and withdrawing substituents at the 3,6-positions of the benzoquinone core, are reported. 1Dy shows an octacoordinated {N6O2} DyIII ion within a D4h distorted square antiprismatic coordination, an ideal geometry for Single-Molecule Magnet (SMM) behavior, given its oblate nature, whereas in 2Dy the octacoordinated DyIII ion adopts a D2d triangular dodecahedron geometry, while maintaining the same {N6O2} coordination sphere. Both complexes show field-induced single molecule magnet (SMM) behaviour, with tuning of the slow magnetic relaxation as a function of the nature of the substituents at the 3,6-positions of the anilate moiety. A comparison of the Arrhenius fitting parameters for 1Dy and 2Dy supports the hypothesis that square antiprismatic DyIII complexes, as 1Dy, exhibit higher energy barriers. This interpretation is supported by ab initio calculations that also shed light on the crucial role of intermolecular dipolar interactions. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2024 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/2072/537606 https://doi.org/10.1039/D4DT00175C |
| url |
http://hdl.handle.net/2072/537606 https://doi.org/10.1039/D4DT00175C |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Fondazione di Sardegna, Convenzione Triennale tra la Fondazione di Sardegna e gli Atenei Sardi, Regione Sardegna, L.R. 7/2007 annualità 2020, through the SMAWRT project (CUP F75F21001260007) MCIN/AEI/10.13039/501100011033/ through project PID2021-124796OB-I00 Generalitat de Catalunya (2021SGR1154) Ministerio de Ciencia e Innovación through the Severo Ochoa Excellence Accreditations CEX2019-000925-S (MCIN/AEI) and CEX2021-001214-S CERCA Programme/Generalitat de Catalunya |
| dc.rights.none.fl_str_mv |
CC-BY info:eu-repo/semantics/openAccess |
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CC-BY |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
25 p. 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 |
RECERCAT (Dipòsit de la Recerca de Catalunya) reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| instname_str |
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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1869411838905548800 |
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15,811543 |