0000000000640269

AUTHOR

Mathieu Rouzières

showing 15 related works from this author

Room-Temperature Magnetic Bistability in a Salt of Organic Radical Ions

2021

International audience; Cocrystallization of 7,7′,8,8′-tetracyanoquinodimethane radical anion (TCNQ −•) and 3-methylpyridinium-1,2,3,5dithiadiazolyl radical cation (3-MepyDTDA +•) afforded isostructural acetonitrile (MeCN) or propionitrile (EtCN) solvates containing cofacial π dimers of homologous components. Loss of lattice solvent from the diamagnetic solvates above 366 K affords a high-temperature paramagnetic phase containing discrete TCNQ −• and weakly bound π dimers of 3-MepyDTDA +• , as evidenced by X-ray diffraction methods and magnetic susceptibility measurements. Below 268 K, a first-order phase transition occurs, leading to a low-temperature diamagnetic phase with TCNQ −• σ dimer…

magneettiset ominaisuudetDimer02 engineering and technologyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry021001 nanoscience & nanotechnologyvapaat radikaalit01 natural sciencesBiochemistryTetracyanoquinodimethaneMagnetic susceptibilityCatalysis0104 chemical scienceschemistry.chemical_compoundParamagnetismCrystallographyColloid and Surface ChemistryRadical ionchemistryDiamagnetismPropionitrileIsostructural0210 nano-technologyorgaaniset yhdisteet
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Role of Alkyl Substituent and Solvent on the Structural, Thermal, and Magnetic Properties of Binary Radical Salts of 1,2,3,5-Dithia- or Diselenadiazo…

2022

The synthesis, structural, thermal, and magnetic properties of a series of simple binary organic salts based on the radical anion of 7,7,8,8-tetracyanoquinodimethane (TCNQ) and 4-(N-alkylpyridinium-3-yl)-1,2,3,5-dithiadiazolyl (DTDA), 1R (R = Et, Pr, Bu), radical cations and their heavier selenium analogues (DSDA), 2R, are described. Single-crystal X-ray structural analyses reveal that short alkyl substituents on the pyridinium moiety of DTDA/DSDA cations lead to crystallization of isostructural acetonitrile (MeCN) solvates 1Et·MeCN, 1Pr·MeCN, 2Et·MeCN, and 2Pr·MeCN with trans-cofacial DTDA radical cation and eclipsed-cofacial TCNQ radical anion dimers. A slight increase in the substituent …

anionitsuolatreaction productssaltskationitGeneral Materials ScienceGeneral ChemistryoligomersCondensed Matter PhysicsanionscationsCrystal Growth & Design
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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
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Coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization in the first lanthanide complex of a 1,2,4-benzotriazinyl …

2017

The first lanthanide complex of a 1,2,4-benzotriazinyl radical (1), Dy(1)(tbacac)3 (2, tbacac = 2,2,6,6-tetramethyl-3,5-heptane-dionato), was synthesised and found to have an antiferromagnetically ordered ground state with a metamagnetic phase diagram and a critical field of 0.91 T at 1.85 K. The application of a small dc field revealed the single-molecule magnet behaviour of 2, illustrating the coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization. peerReviewed

LanthanideCondensed matter physics010405 organic chemistryChemistryRelaxation (NMR)[CHIM.MATE]Chemical Sciences/Material chemistrykompleksiyhdisteetharvinaiset maametallit010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryMagnetizationMagnetmagnetismAntiferromagnetismcoordination complexesmagnetismiGround staterare earth metalsCritical fieldta116ComputingMilieux_MISCELLANEOUSPhase diagram
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Metal-organic magnets with large coercivity and ordering temperatures up to 242°C.

2020

International audience; Magnets derived from inorganic materials (e.g., oxides, rare-earth–based, and intermetallic compounds) are key components of modern technological applications. Despite considerable success in a broad range of applications, these inorganic magnets suffer several drawbacks, including energetically expensive fabrication, limited availability of certain constituent elements, high density, and poor scope for chemical tunability. A promising design strategy for next-generation magnets relies on the versatile coordination chemistry of abundant metal ions and inexpensive organic ligands. Following this approach, we report the general, simple, and efficient synthesis of light…

FabricationMaterials sciencemagneettiset ominaisuudetPyrazineMetal ions in aqueous solutionmagneetitIntermetallicNanotechnology02 engineering and technologyorganometalliyhdisteet010402 general chemistrylarge coercivity7. Clean energy01 natural sciencesordering temperaturesCoordination complexchemistry.chemical_compoundMoleculechemistry.chemical_classificationMultidisciplinarymetal-organic magnets[CHIM.MATE]Chemical Sciences/Material chemistrykompleksiyhdisteetCoercivity021001 nanoscience & nanotechnologykiteet0104 chemical scienceschemistryMagnetlämpötila0210 nano-technologyScience (New York, N.Y.)
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CCDC 1057508: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal SystemCrystal Structurebis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-cobalt(ii)Cell ParametersExperimental 3D Coordinates
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CCDC 1057512: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal System1-Phenyl-3-(pyridin-2-yl)-14-dihydro-124-benzotriazineCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1983877: Experimental Crystal Structure Determination

2020

Related Article: Panagiota Perlepe, Itziar Oyarzabal, Aaron Mailman, Morgane Yquel, Mikhail Platunov, Iurii Dovgaliuk, Mathieu Rouzières, Philippe Négrier, Denise Mondieig, Elizaveta A. Suturina, Marie-Anne Dourges, Sébastien Bonhommeau, Rebecca A. Musgrave, Kasper S. Pedersen, Dmitry Chernyshov, Fabrice Wilhelm, Andrei Rogalev, Corine Mathonière, Rodolphe Clérac|2020|Science|6516|587|doi:10.1126/science.abb3861

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[lithium chloride bis(mu-pyrazine radical cation)-chromium(ii) tetrahydrofuran solvate]Experimental 3D Coordinates
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CCDC 1057511: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersNN'-Diphenylpyridine-2-carbohydrazonamideExperimental 3D Coordinates
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CCDC 1057510: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal SystemCrystal StructureN-Phenylpyridine-2-carbothioamideCell ParametersExperimental 3D Coordinates
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CCDC 1057507: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

bis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-iron(ii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1057506: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

bis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-manganese(ii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2007863: Experimental Crystal Structure Determination

2020

Related Article: Panagiota Perlepe, Itziar Oyarzabal, Aaron Mailman, Morgane Yquel, Mikhail Platunov, Iurii Dovgaliuk, Mathieu Rouzières, Philippe Négrier, Denise Mondieig, Elizaveta A. Suturina, Marie-Anne Dourges, Sébastien Bonhommeau, Rebecca A. Musgrave, Kasper S. Pedersen, Dmitry Chernyshov, Fabrice Wilhelm, Andrei Rogalev, Corine Mathonière, Rodolphe Clérac|2020|Science|6516|587|doi:10.1126/science.abb3861

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[lithium chloride bis(mu-pyrazine radical cation)-chromium(ii) tetrahydrofuran solvate]Experimental 3D Coordinates
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CCDC 1563199: Experimental Crystal Structure Determination

2017

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Mathieu Rouzières, Rodolphe Clérac, Heikki M. Tuononen|2017|Dalton Trans.|46|12790|doi:10.1039/C7DT02766D

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterstris(acetylacetonato)-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-dysprosium(iii)Experimental 3D Coordinates
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CCDC 1057509: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal Systembis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-nickel(ii)Crystal StructureCell ParametersExperimental 3D Coordinates
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