0000000000420232

AUTHOR

Maria Luz Godino-salido

0000-0003-3257-4431

showing 5 related works from this author

Polyfunctional Tetraaza-Macrocyclic Ligands: Zn(II), Cu(II) Binding and Formation of Hybrid Materials with Multiwalled Carbon Nanotubes

2017

The binding properties of HL1, HL2, and HL3 ligands toward Cu(II) and Zn(II) ions, constituted by tetraaza-macrocyclic rings decorated with pyrimidine pendants, were investigated by means of potentiometric and UV spectrophotometric measurements in aqueous solution, with the objective of using the related HL-M(II) (HL = HL1–HL3; M = Cu, Zn) complexes for the preparation of hybrid MWCNT-HL-M(II) materials based on multiwalled carbon nanotubes (MWCNTs), through an environmentally friendly noncovalent procedure. As shown by the crystal structure of [Cu(HL1)](ClO4)2, metal coordination takes place in the macrocyclic ring, whereas the pyrimidine residue remains available for attachment onto the s…

Aqueous solutionMaterials sciencePyrimidine010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryPotentiometric titrationStackingGeneral ChemistryCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesArticle0104 chemical sciencesMetallcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999visual_artPolymer chemistryvisual_art.visual_art_mediumHybrid materialcarbon nanotubes copper zinc macrocycles hybrid materials functionalized carbon nanotubesACS Omega
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Thermodynamic and fluorescence emission studies on chemosensors containing anthracene fluorophores. Crystal structure of {[CuL1Cl]Cl}2·2H2O [L1 = N-(…

1999

The co-ordination capabilities toward hydrogen ions, Co2+, Ni2+, Cu2+, Zn2+ and Cd2+ of the novel receptor 2,6,9,13-tetraaza[14](9,10)anthracenophane (L) and of its open-chain counterpart N-(3-aminopropyl)-N′-3-(anthracen-9-ylmethyl)aminopropylethane-1,2-diamine (L1) is described. Stepwise protonation constants of the cyclic receptor (L) are lower than those of the open-chain receptor (L1) . Quenching effects of the fluorescence emission occur upon first and second deprotonation of L and upon second deprotonation of L1. Stability constants of the Co2+, Ni2+, Cu2+, Zn2+ and Cd2+ complexes follow the Irving–Williams trend and are intermediate between those of triethylenetetraamine with termin…

Anthracenechemistry.chemical_compoundCrystallographyDeprotonationQuenching (fluorescence)chemistrySquare pyramidProtonationGeneral ChemistryCrystal structureTriclinic crystal systemPhotochemistrySquare pyramidal molecular geometry
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A New Heterogeneous Catalyst Obtained via Supramolecular Decoration of Graphene with a Pd2+ Azamacrocyclic Complex

2019

A new G-(H2L)-Pd heterogeneous catalyst has been prepared via a self-assembly process consisting in the spontaneous adsorption, in water at room temperature, of a macrocyclic H2L ligand on graphene (G) (G + H2L = G-(H2L)), followed by decoration of the macrocycle with Pd2+ ions (G-(H2L) + Pd2+ = G-(H2L)-Pd) under the same mild conditions. This supramolecular approach is a sustainable (green) procedure that preserves the special characteristics of graphene and furnishes an efficient catalyst for the Cu-free Sonogashira cross coupling reaction between iodobenzene and phenylacetylene. Indeed, G-(H2L)-Pd shows an excellent conversion (90%) of reactants into diphenylacetylene under mild conditio…

Models MolecularChemical PhenomenaIodobenzeneMolecular ConformationPharmaceutical ScienceSonogashira couplingLigands010402 general chemistryHeterogeneous catalysiscross coupling01 natural sciencesArticleCoupling reactionAnalytical Chemistrylaw.inventionCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryCoordination ComplexeslawDrug DiscoveryPolymer chemistryPhysical and Theoretical ChemistryDiphenylacetyleneMolecular Structurecatalysis010405 organic chemistryGrapheneSpectrum AnalysisOrganic ChemistrySonogashirapalladium catalystHydrogen-Ion Concentrationsupramolecular interactions0104 chemical sciencesSolutionsazamacrocycleschemistryPhenylacetyleneChemistry (miscellaneous)surface adsorptionMolecular MedicineGraphitecatalysis palladium catalyst; Sonogashira graphenePalladiumMolecules
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Construction of green nanostructured heterogeneous catalysts via non-covalent surface decoration of multi-walled carbon nanotubes with Pd(II) complex…

2017

Abstract Green nanostructured heterogeneous catalysts were prepared via a bottom-up strategy. Designed ligands were synthesized joining covalently an electrondeficient pyrimidine residue and a scorpiand azamacrocycle. The desired molecular properties were easily transferred to nanostructured materials in two steps: first, exploiting their spontaneous chemisorption onto multi-walled carbon nanotubes (MWCNTs) via the pyrimidinic moiety in water at room temperature, then, taking advantage of the easy coordination of Pd(II) to the azamacrocycle in the same conditions. An evenly distribution of catalytic centres was obtained on the MWCNTs surface. Catalytic properties of these materials were ass…

ChemistryAzamacrocycles Hybrid materials Multi-walled carbon nanotubes Non-covalent functionalization Palladium(II) catalysis Sonogashira cross coupling CatalysisSonogashira coupling02 engineering and technologyCarbon nanotube010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical scienceslaw.inventionCatalysisResidue (chemistry)Chemical engineeringlawCovalent bondChemisorptionMoietyOrganic chemistryPhysical and Theoretical Chemistry0210 nano-technologyHybrid material
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CCDC 1553257: Experimental Crystal Structure Determination

2017

Related Article: Matteo Savastano, Paloma Arranz-Mascaros, ́Carla Bazzicalupi, Maria Paz Clares, Maria Luz Godino-Salido, Lluis Guijarro, Maria Dolores Gutierrez-Valero, ́Antonio Bianchi, Enrique García-España, Rafael Lopez-Garzon|2017|ACS Omega|2|3868|doi:10.1021/acsomega.7b00736

Space GroupCrystallographycatena-[(mu-6-amino-3-methyl-5-nitroso-2-({2-[36915-tetraazabicyclo[9.3.1]pentadeca-1(15)1113-trien-6-yl]ethyl}amino)pyrimidin-4(3H)-one)-copper(ii) diperchlorate]Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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