Jean-pierre Costes - Academia.edu (original) (raw)
Papers by Jean-pierre Costes
Organic magnetic resonance, Feb 1, 1975
L'étude par résonance magnétique nucléaire (11B) des systèmes formés par le tripropylbore et ... more L'étude par résonance magnétique nucléaire (11B) des systèmes formés par le tripropylbore et l'anhydride borique met en évidence l'intervention de réactions de redistribution entre le tripropylbore et ses produits d'oxydation, c'est‐à‐dire de redistributions mettant en jeu des groupements monofonctionnels (C3H7) et difonctionnels (O) sur des atomes de bore tricoordonnés.
Dalton Transactions, 2019
The observed 155Gd Mössbauer isomer shifts of 3d–Gd complexes give an experimental proof for the ... more The observed 155Gd Mössbauer isomer shifts of 3d–Gd complexes give an experimental proof for the participation of 5d Gd orbitals to the magnetic interaction in these 3d–Gd complexes.
Canadian Journal of Chemistry, Oct 1, 1976
A study by 11B and 1H nmr of the scrambling reactions between the boron trihalides BX3 (X = I, Br... more A study by 11B and 1H nmr of the scrambling reactions between the boron trihalides BX3 (X = I, Br, Cl, F) and the trialkylborane BR3 (R = C3H7, C4H9) shows that the mixed species, on equilibrium are non uniformly favoured. The effects of Lewis acidity and steric hindrance are discussed.
Chemical Communications, 2005
European Journal of Inorganic Chemistry, Dec 1, 2009
ABSTRACT The synthesis and characterization of copper(II), manganese(III), and iron(III) complexe... more ABSTRACT The synthesis and characterization of copper(II), manganese(III), and iron(III) complexes [Cu2(L1)(OAc)Cs2(MeOH)2]n (1), [Mn2(H3L1)2(OMe)2]·2MeOH (2), [Fe2(H3L1)2(Hpz)4](ClO4)2·2CH3CN (3), and [Fe2(H3L3)2(OMe)2]·8MeOH (4) of potentially pentaanionic heptadentate ligands,2-hydroxy-N-{2-hydroxy-3-[(2-hydroxybenzoyl)amino]propyl}benzamide (H5L1) and 2-hydroxy-N-{3-hydroxy-5-[(2-hydroxybenzoyl)amino]pentyl}benzamide (H5L3), are reported. The crystal structure and magnetic properties of these complexes have been determined. In complex 1, the ligand H5L1 acts as a heptadentate, fully deprotonated ligand, [L1]5-. In complexes 2, 3, and 4, H5L1 (2, 3) and H5L3 (4) act as tetradentate, partially deprotonated ligands, [H3L1]2- and [H3L3]2-.In complex 1, anionic [Cu2(L1)(OAc)]2- and cationic [Cs(MeOH)]+ units are linked through a quadruply bridging acetate ion and through the phenoxido-oxygen and amido-oxygen donor atoms of [L1]5- to yield a 2D polymeric network. Complexes 2-4 form extended supramolecular networks. Magnetic susceptibility data evidence antiferromagnetic interactions for 1, 2, and 4. The Fe···Fe distance is too long to allow measurable magnetic interactions in complex 3.
Inorganic Chemistry, May 1, 1989
Inorganic Chemistry, Feb 12, 1997
ABSTRACT
Inorganic Chemistry, May 1, 1995
Polyhedron, May 1, 2009
ABSTRACT
Inorganica Chimica Acta, Nov 1, 1995
Inorganic Chemistry, Jun 15, 2009
The syntheses, structural determinations, and magnetic studies of two trinuclear Ni-Gd-Ni complex... more The syntheses, structural determinations, and magnetic studies of two trinuclear Ni-Gd-Ni complexes are described. The structural studies demonstrate that the two complexes present a linear arrangement of the Ni and Gd ions, with Ni ions in slightly distorted square-pyramidal or octahedral environments in complexes 1 and 2, respectively. The Ni and Gd ions are linked by two or three phenoxo bridges, so that complexes 1 and 2 present edge-sharing or face-sharing bridging cores. Ferromagnetic interactions operate in these complexes. While a unique J parameter is able to fit the magnetic data of complex 2, two very different J constants are needed for 1. This result is at first sight surprising, for the structural data of the two Ni-O(2)-Gd cores in complex 1 are quite similar (similar Ni-O and Gd-O bond lengths, similar angles, and dihedral angles), the only difference coming from the angle between the planes defined by the Gd ion and the two bridging phenoxo oxygen atoms of each Ni-O(2)-Gd half core. This latter magnetic behavior can be considered as a signature for the participation of 5d Gd(III) orbitals in the exchange interaction mechanism and can explain why edge-sharing complexes have larger J parameters than face-sharing complexes.
Inorganic Chemistry, Sep 6, 2003
Journal of The Chemical Society-dalton Transactions, 1988
ABSTRACT
Inorganica Chimica Acta, Mar 1, 1995
... Chem., 23 (1984) 1620. [10] F. Lloret, M. Julve, J. Faus, Y. Journaux, M. PhilocheLevisalles ... more ... Chem., 23 (1984) 1620. [10] F. Lloret, M. Julve, J. Faus, Y. Journaux, M. PhilocheLevisalles and Y. Jeannin, Inorg. Chem., 28 (1989) 3702. [11] F. Lloret, M. Julve, J. Faus, R. Ruiz, I. Castro, M. Mollar and M. PhilocheLevisalles, Inorg. Chem., 31 (1992) 784. ...
Dalton Transactions, 2019
Inorganica Chimica Acta, Jul 1, 1990
Inorganic Chemistry, Aug 1, 1994
... Jean-Pierre Costes,t Franqoise Dahan,+ Jose Manuel Dominguez-Vera,# Jean-Pierre Laurent,**t J... more ... Jean-Pierre Costes,t Franqoise Dahan,+ Jose Manuel Dominguez-Vera,# Jean-Pierre Laurent,**t Jose Ruiz,* and Jean Sotiropouloss ... (3) Costes, J.-P.; Dahan, F.; Laurent, J.-P. Inorg. Chem. 1991, 30, 1887. (4) Costes, J.-P.; Dominguez-Vera, J. M.; Laurent, J.-P. 29th ICCC. ...
European Journal of Inorganic Chemistry, Aug 19, 2009
The synthesis, structural determination and magnetic study of a trinuclear MnII–GdIII–MnII comple... more The synthesis, structural determination and magnetic study of a trinuclear MnII–GdIII–MnII complex involving a Schiff base ligand are described. The structural study demonstrates that the complex presents a linear arrangement of the Mn and Gd ions, with hexacoordinate Mn ions in slightly distorted or distorted trigonal prism environments and nine‐coordinate gadolinium ions. The Mn and Gd ions are linked by two phenoxido bridges for one Mn–Gd subunit and two phenoxido plus one nitrato bridges for the other Mn–Gd subunit. Ferromagnetic interactions operate in the complex. The best fit takes into account two different J constants and D and E zero‐field splitting terms. A strict 3d‐5d(Gd) orthogonality is not possible in the present complex because all 3d orbitals of the Mn ions are occupied, which does agree with the weak value of the JMn,Gd parameter. Oxidation of this complex does not yield the corresponding MnIII–GdIII–MnIII entity.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Dalton Transactions, 2010
Organic magnetic resonance, Feb 1, 1975
L'étude par résonance magnétique nucléaire (11B) des systèmes formés par le tripropylbore et ... more L'étude par résonance magnétique nucléaire (11B) des systèmes formés par le tripropylbore et l'anhydride borique met en évidence l'intervention de réactions de redistribution entre le tripropylbore et ses produits d'oxydation, c'est‐à‐dire de redistributions mettant en jeu des groupements monofonctionnels (C3H7) et difonctionnels (O) sur des atomes de bore tricoordonnés.
Dalton Transactions, 2019
The observed 155Gd Mössbauer isomer shifts of 3d–Gd complexes give an experimental proof for the ... more The observed 155Gd Mössbauer isomer shifts of 3d–Gd complexes give an experimental proof for the participation of 5d Gd orbitals to the magnetic interaction in these 3d–Gd complexes.
Canadian Journal of Chemistry, Oct 1, 1976
A study by 11B and 1H nmr of the scrambling reactions between the boron trihalides BX3 (X = I, Br... more A study by 11B and 1H nmr of the scrambling reactions between the boron trihalides BX3 (X = I, Br, Cl, F) and the trialkylborane BR3 (R = C3H7, C4H9) shows that the mixed species, on equilibrium are non uniformly favoured. The effects of Lewis acidity and steric hindrance are discussed.
Chemical Communications, 2005
European Journal of Inorganic Chemistry, Dec 1, 2009
ABSTRACT The synthesis and characterization of copper(II), manganese(III), and iron(III) complexe... more ABSTRACT The synthesis and characterization of copper(II), manganese(III), and iron(III) complexes [Cu2(L1)(OAc)Cs2(MeOH)2]n (1), [Mn2(H3L1)2(OMe)2]·2MeOH (2), [Fe2(H3L1)2(Hpz)4](ClO4)2·2CH3CN (3), and [Fe2(H3L3)2(OMe)2]·8MeOH (4) of potentially pentaanionic heptadentate ligands,2-hydroxy-N-{2-hydroxy-3-[(2-hydroxybenzoyl)amino]propyl}benzamide (H5L1) and 2-hydroxy-N-{3-hydroxy-5-[(2-hydroxybenzoyl)amino]pentyl}benzamide (H5L3), are reported. The crystal structure and magnetic properties of these complexes have been determined. In complex 1, the ligand H5L1 acts as a heptadentate, fully deprotonated ligand, [L1]5-. In complexes 2, 3, and 4, H5L1 (2, 3) and H5L3 (4) act as tetradentate, partially deprotonated ligands, [H3L1]2- and [H3L3]2-.In complex 1, anionic [Cu2(L1)(OAc)]2- and cationic [Cs(MeOH)]+ units are linked through a quadruply bridging acetate ion and through the phenoxido-oxygen and amido-oxygen donor atoms of [L1]5- to yield a 2D polymeric network. Complexes 2-4 form extended supramolecular networks. Magnetic susceptibility data evidence antiferromagnetic interactions for 1, 2, and 4. The Fe···Fe distance is too long to allow measurable magnetic interactions in complex 3.
Inorganic Chemistry, May 1, 1989
Inorganic Chemistry, Feb 12, 1997
ABSTRACT
Inorganic Chemistry, May 1, 1995
Polyhedron, May 1, 2009
ABSTRACT
Inorganica Chimica Acta, Nov 1, 1995
Inorganic Chemistry, Jun 15, 2009
The syntheses, structural determinations, and magnetic studies of two trinuclear Ni-Gd-Ni complex... more The syntheses, structural determinations, and magnetic studies of two trinuclear Ni-Gd-Ni complexes are described. The structural studies demonstrate that the two complexes present a linear arrangement of the Ni and Gd ions, with Ni ions in slightly distorted square-pyramidal or octahedral environments in complexes 1 and 2, respectively. The Ni and Gd ions are linked by two or three phenoxo bridges, so that complexes 1 and 2 present edge-sharing or face-sharing bridging cores. Ferromagnetic interactions operate in these complexes. While a unique J parameter is able to fit the magnetic data of complex 2, two very different J constants are needed for 1. This result is at first sight surprising, for the structural data of the two Ni-O(2)-Gd cores in complex 1 are quite similar (similar Ni-O and Gd-O bond lengths, similar angles, and dihedral angles), the only difference coming from the angle between the planes defined by the Gd ion and the two bridging phenoxo oxygen atoms of each Ni-O(2)-Gd half core. This latter magnetic behavior can be considered as a signature for the participation of 5d Gd(III) orbitals in the exchange interaction mechanism and can explain why edge-sharing complexes have larger J parameters than face-sharing complexes.
Inorganic Chemistry, Sep 6, 2003
Journal of The Chemical Society-dalton Transactions, 1988
ABSTRACT
Inorganica Chimica Acta, Mar 1, 1995
... Chem., 23 (1984) 1620. [10] F. Lloret, M. Julve, J. Faus, Y. Journaux, M. PhilocheLevisalles ... more ... Chem., 23 (1984) 1620. [10] F. Lloret, M. Julve, J. Faus, Y. Journaux, M. PhilocheLevisalles and Y. Jeannin, Inorg. Chem., 28 (1989) 3702. [11] F. Lloret, M. Julve, J. Faus, R. Ruiz, I. Castro, M. Mollar and M. PhilocheLevisalles, Inorg. Chem., 31 (1992) 784. ...
Dalton Transactions, 2019
Inorganica Chimica Acta, Jul 1, 1990
Inorganic Chemistry, Aug 1, 1994
... Jean-Pierre Costes,t Franqoise Dahan,+ Jose Manuel Dominguez-Vera,# Jean-Pierre Laurent,**t J... more ... Jean-Pierre Costes,t Franqoise Dahan,+ Jose Manuel Dominguez-Vera,# Jean-Pierre Laurent,**t Jose Ruiz,* and Jean Sotiropouloss ... (3) Costes, J.-P.; Dahan, F.; Laurent, J.-P. Inorg. Chem. 1991, 30, 1887. (4) Costes, J.-P.; Dominguez-Vera, J. M.; Laurent, J.-P. 29th ICCC. ...
European Journal of Inorganic Chemistry, Aug 19, 2009
The synthesis, structural determination and magnetic study of a trinuclear MnII–GdIII–MnII comple... more The synthesis, structural determination and magnetic study of a trinuclear MnII–GdIII–MnII complex involving a Schiff base ligand are described. The structural study demonstrates that the complex presents a linear arrangement of the Mn and Gd ions, with hexacoordinate Mn ions in slightly distorted or distorted trigonal prism environments and nine‐coordinate gadolinium ions. The Mn and Gd ions are linked by two phenoxido bridges for one Mn–Gd subunit and two phenoxido plus one nitrato bridges for the other Mn–Gd subunit. Ferromagnetic interactions operate in the complex. The best fit takes into account two different J constants and D and E zero‐field splitting terms. A strict 3d‐5d(Gd) orthogonality is not possible in the present complex because all 3d orbitals of the Mn ions are occupied, which does agree with the weak value of the JMn,Gd parameter. Oxidation of this complex does not yield the corresponding MnIII–GdIII–MnIII entity.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Dalton Transactions, 2010