6533b855fe1ef96bd12b126a
RESEARCH PRODUCT
Syntheses, characterisation, magnetism and photoluminescence of a homodinuclear Ln(III)-Schiff base family.
Joy ChakrabortyRaymond ZiesselLoïc J. CharbonnièreM. S. El FallahLuca M. CarrellaAurkie RayEva RentschlerDominique LuneauGuillaume PiletSamiran MitraGuillaume Chastanetsubject
LanthanideSchiff base010405 organic chemistryStereochemistryLigandMetal ions in aqueous solution[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artDiethylenetriamine[CHIM.CRIS]Chemical Sciences/Cristallographyvisual_art.visual_art_medium[CHIM]Chemical SciencesSingle crystaldescription
A novel family of homodinuclear complexes of the general formula [Ln(2)L(2)(X)(2)] (where Ln = Nd(3+), Pr(3+), Sm(3+) and Tb(3+) for 1, 2, 3 and 4, respectively and X, the coordinated NO(3)(-) or Cl(-) anion) has been synthesised from the corresponding lanthanide(III) salts with the pentadentate dianionic Schiff base ligand, H(2)L [N(1),N(3)-bis(salicylideneimino)diethylenetriamine], that exhibits a N(3)O(2) donor set. Single crystal X-ray diffraction studies evidenced the isostructurality of this family of centrosymmetric neutral dinuclear entities where the Ln(III) metal centres are coupled together by two phenolato oxygen atoms belonging to two units of ligand (H(2)L). Interestingly, the two other phenolato groups of H(2)L are mono-coordinated to the metal ions. Temperature dependence (2-300K) magnetic susceptibility studies suggest the presence of an antiferromagnetic interaction operating via double phenolato bridges. Photoluminescence activities of the complexes have been studied and compared with their precursor ligand. All the complexes have been characterised with microanalytical and several spectroscopic techniques.
year | journal | country | edition | language |
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2009-11-19 | Dalton transactions (Cambridge, England : 2003) |