Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand

The reactions between the bis(1,10-phenantro[5,6-b])tetrathiafulvalene triad (L) and the metallo-precursors Yb(hfac)<sub>3</sub>(H<sub>2</sub>O)<sub>2</sub> (hfac<sup>−</sup> = 1,1,1,5,5,5-hexafluoroacetylacetonato anion) and Dy(facam)<sub>3</...

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Main Authors: Bertrand Lefeuvre, Jessica Flores Gonzalez, Carlo Andrea Mattei, Vincent Dorcet, Olivier Cador, Fabrice Pointillart
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Inorganics
Subjects:
Online Access:https://www.mdpi.com/2304-6740/9/7/50
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spelling doaj-7b6df97bd1594359bef4fcafc32173aa2021-07-23T13:47:17ZengMDPI AGInorganics2304-67402021-06-019505010.3390/inorganics9070050Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad LigandBertrand Lefeuvre0Jessica Flores Gonzalez1Carlo Andrea Mattei2Vincent Dorcet3Olivier Cador4Fabrice Pointillart5ISCR (Institut des Sciences Chimiques de Rennes)—UMR-CNRS 6226, Université de Rennes, 35000 Rennes, FranceISCR (Institut des Sciences Chimiques de Rennes)—UMR-CNRS 6226, Université de Rennes, 35000 Rennes, FranceISCR (Institut des Sciences Chimiques de Rennes)—UMR-CNRS 6226, Université de Rennes, 35000 Rennes, FranceISCR (Institut des Sciences Chimiques de Rennes)—UMR-CNRS 6226, Université de Rennes, 35000 Rennes, FranceISCR (Institut des Sciences Chimiques de Rennes)—UMR-CNRS 6226, Université de Rennes, 35000 Rennes, FranceISCR (Institut des Sciences Chimiques de Rennes)—UMR-CNRS 6226, Université de Rennes, 35000 Rennes, FranceThe reactions between the bis(1,10-phenantro[5,6-b])tetrathiafulvalene triad (L) and the metallo-precursors Yb(hfac)<sub>3</sub>(H<sub>2</sub>O)<sub>2</sub> (hfac<sup>−</sup> = 1,1,1,5,5,5-hexafluoroacetylacetonato anion) and Dy(facam)<sub>3</sub> (facam<sup>−</sup> = 3-trifluoro-acetyl-(+)-camphorato anion) lead to the formation of two dinuclear complexes of formula [Yb<sub>2</sub>(hfac)<sub>6</sub>(L)]·2(C<sub>7</sub>H<sub>16</sub>) ((<b>1</b>)·2(C<sub>7</sub>H<sub>16</sub>)) and [Dy<sub>2</sub>((+)facam)<sub>6</sub>(L)]·2(C<sub>6</sub>H<sub>14</sub>) ((<b>2</b>)·2(C<sub>6</sub>H<sub>14</sub>)). The X-ray structures reveal that the L triad bridges two terminal Yb(hfac)<sub>3</sub> or Dy(facam)<sub>3</sub> units. (<b>1</b>)·2(C<sub>7</sub>H<sub>16</sub>) behaved as a near infrared Yb<sup>III</sup> centered emitter and a field-induced Single-Molecule Magnet (SMM) while (<b>2</b>)·2(C<sub>6</sub>H<sub>14</sub>) displayed SMM behavior in both zero- and in-dc field. The magnetization mainly relaxes through a Raman process for both complexes under an optimal applied magnetic field.https://www.mdpi.com/2304-6740/9/7/50tetrathiafulvalenetriadslanthanideschiralityluminescencesingle-molecule magnet
collection DOAJ
language English
format Article
sources DOAJ
author Bertrand Lefeuvre
Jessica Flores Gonzalez
Carlo Andrea Mattei
Vincent Dorcet
Olivier Cador
Fabrice Pointillart
spellingShingle Bertrand Lefeuvre
Jessica Flores Gonzalez
Carlo Andrea Mattei
Vincent Dorcet
Olivier Cador
Fabrice Pointillart
Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand
Inorganics
tetrathiafulvalene
triads
lanthanides
chirality
luminescence
single-molecule magnet
author_facet Bertrand Lefeuvre
Jessica Flores Gonzalez
Carlo Andrea Mattei
Vincent Dorcet
Olivier Cador
Fabrice Pointillart
author_sort Bertrand Lefeuvre
title Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand
title_short Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand
title_full Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand
title_fullStr Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand
title_full_unstemmed Chiral or Luminescent Lanthanide Single-Molecule Magnets Involving Bridging Redox Active Triad Ligand
title_sort chiral or luminescent lanthanide single-molecule magnets involving bridging redox active triad ligand
publisher MDPI AG
series Inorganics
issn 2304-6740
publishDate 2021-06-01
description The reactions between the bis(1,10-phenantro[5,6-b])tetrathiafulvalene triad (L) and the metallo-precursors Yb(hfac)<sub>3</sub>(H<sub>2</sub>O)<sub>2</sub> (hfac<sup>−</sup> = 1,1,1,5,5,5-hexafluoroacetylacetonato anion) and Dy(facam)<sub>3</sub> (facam<sup>−</sup> = 3-trifluoro-acetyl-(+)-camphorato anion) lead to the formation of two dinuclear complexes of formula [Yb<sub>2</sub>(hfac)<sub>6</sub>(L)]·2(C<sub>7</sub>H<sub>16</sub>) ((<b>1</b>)·2(C<sub>7</sub>H<sub>16</sub>)) and [Dy<sub>2</sub>((+)facam)<sub>6</sub>(L)]·2(C<sub>6</sub>H<sub>14</sub>) ((<b>2</b>)·2(C<sub>6</sub>H<sub>14</sub>)). The X-ray structures reveal that the L triad bridges two terminal Yb(hfac)<sub>3</sub> or Dy(facam)<sub>3</sub> units. (<b>1</b>)·2(C<sub>7</sub>H<sub>16</sub>) behaved as a near infrared Yb<sup>III</sup> centered emitter and a field-induced Single-Molecule Magnet (SMM) while (<b>2</b>)·2(C<sub>6</sub>H<sub>14</sub>) displayed SMM behavior in both zero- and in-dc field. The magnetization mainly relaxes through a Raman process for both complexes under an optimal applied magnetic field.
topic tetrathiafulvalene
triads
lanthanides
chirality
luminescence
single-molecule magnet
url https://www.mdpi.com/2304-6740/9/7/50
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