0000000000017957

AUTHOR

José Sánchez Costa

0000-0001-5426-7956

showing 3 related works from this author

Remarkable Steric Effects and Influence of Monodentate Axial Ligands L on the Spin-Crossover Properties of trans-[FeII(N4 ligand)L] Complexes

2007

Iron(II) complexes obtained from tetradentate, rigid, linear N4 ligands have been investigated to appraise the influence of steric effects and the impact of trans-coordinated anions on the spin-transition behavior. As expected, the well-designed ligands embrace the metal center, resulting in octahedral iron(II) complexes where the basal plane is fully occupied by the pyridine/pyrazole N4 ligand, while anions or solvent molecules are exclusively axially coordinated. Precursor complexes, namely, [Fe(bpzbpy)(MeOH)2](BF4)2 (where bpzbpy symbolizes the ligand 6,6'-bis(N-pyrazolylmethyl)-2,2'-bipyridine) and [Fe(mbpzbpy)(MeOH)2](BF4)2 (where mbpzbpy symbolizes the ligand 6,6'-bis(3,5-dimethyl-N-p…

Steric effectsDenticityTetradentate ligandThiocyanateMössbauer spectroscopy010405 organic chemistryLigandStereochemistry[CHIM.MATE]Chemical Sciences/Material chemistryIron complexesPyrazoleSpin crossover010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySpin crossoverPyridinePhysical and Theoretical ChemistryDicyanamideInorganic Chemistry
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Divergent Adsorption-Dependent Luminescence of Amino-Functionalized Lanthanide Metal-Organic Frameworks for Highly Sensitive NO2 Sensors

2020

International audience; A novel gas sensing mechanism exploiting lanthanide luminescence modulation upon NO2 adsorption is demonstrated here. Two isostructural lanthanide-based metal–organic frameworks (MOFs) are used, including an amino group as the sensitive recognition center for NO2 molecules. The transfer of energy from the organic ligands to Ln is strongly dependent on the presence of NO2, resulting in an unprecedented photoluminescent sensing scheme. Thereby, NO2 exposition triggers either a reversible enhancement or a decrease in the luminescence intensity, depending on the lanthanide ion (Eu or Tb). Our experimental studies combined with density functional theory and complete activ…

LanthanideIonsPhotoluminescenceLuminescenceChemistryLigandAb initioMetal organic frameworks02 engineering and technology[CHIM.MATE]Chemical Sciences/Material chemistryMolecules010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryLigands01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryAdsorptionGeneral Materials ScienceMetal-organic frameworkPhysical and Theoretical ChemistryIsostructural0210 nano-technologyLuminescence
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Photomagnetic properties of an Iron(II) low-spin complex with an unusually long-lived metastable LIESST state

2007

A comprehensive study of the photomagnetic behavior of the [Fe(L222N5)(CN)2].H2O complex has been carried out. This complex is characterized by a low-spin (LS) iron(II)-metal center up to 400 K and exhibits at 10 K the well-known Light-Induced Excited Spin State Trapping (LIESST) effect. The critical LIESST temperature (T(LIESST)) has been measured to be 105 K. The kinetics of the transition from the metastable high-spin (HS) state to the low-spin state have been determined and used for reproducing the experimental T(LIESST) curve. This study represents a second example of a fully low-spin iron(II)-metal complex up to 400 K, which can be photoexcited at low temperature with an atypical long…

Coordination sphereSpin states010405 organic chemistryChemistryKineticsCyanideTrappingMacrocyclic Schiff-base ligand[CHIM.MATE]Chemical Sciences/Material chemistryIron complexes010402 general chemistry01 natural sciencesLIESST0104 chemical sciencesInorganic ChemistryCrystallographyComputational chemistryExcited stateMetastabilityLIESSTPhysical and Theoretical ChemistrySpin (physics)
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