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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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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