0000000001320361

AUTHOR

Luca Fusaro

showing 14 related works from this author

Sintesi e studio fotofisico di sistemi Eu@POSS: controllo dell’emissione attraverso isomeria cis-trans.

EmissionPolyhedral Oligomeric Silsesquioxane POSScis/tran
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Light-induced trans-cis isomerization of terpyridine functionalized POSS nanostructures self-assembled in presence of Eu3+ ions

Eu3+Polyhedral Oligomeric Silsesquioxane (POSS)FluorescenceSensor
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Bisoxazoline-Fullerene Hybrid Systems for Asymmetric Catalysis

FullereneChiralAsymmetricBisoxazoline (BOX)Catalysi
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Cover Feature: Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self‐Assemble in the Presence of Europium(III) Ion…

2020

Materials scienceNanostructurechemistry.chemical_elementGeneral ChemistryPhotochemistrySilsesquioxanechemistry.chemical_compoundchemistryFeature (computer vision)Cover (algebra)Self-assemblyEuropiumLuminescenceIsomerizationChemPlusChem
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White light emitting silsesquioxane based materials: the importance of a ligand with rigid and directional arms

2022

The synthesis of a novel polyhedral oligomeric silsesquioxane functionalized with eight rigid and directional terpyridine-based arms (Ter-POSS) was successfully achieved via a Sonogashira reaction. The POSS based ligand was extensively characterized using different techniques including 1H, 13C and 29Si NMR as well as UV-Vis and fluorescence spectroscopies. The assembly of these nano-caged units in the presence of different transition metal ions (Fe2+, Zn2+ and Cu2+) as well as of a cation from the lanthanides (Eu3+) was investigated using absorption and emission spectroscopies. The final materials display an evident emission in different regions of the visible spectrum as a function of the …

LanthanidePOSS supramolecular chemistry lanthanidesMaterials scienceNanostructurechemistry.chemical_elementQuantum yieldSettore CHIM/06 - Chimica OrganicaFluorescenceSilsesquioxanechemistry.chemical_compoundCrystallographychemistryChemistry (miscellaneous)General Materials ScienceTerpyridineEuropiumVisible spectrumMaterials Advances
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Direct detection of 17O NMR in [Gd(DOTA)]- by NMR Spectroscopy

2015

The 17O NMR spectrum of the non-coordinated carboxyl oxygen in the GdIII-DOTA (DOTA = tetraazacyclododecanetetraacetic acid) complex has been observed experimentally. Its line width is essentially unaffected by paramagnetic relaxation due to gadolinium, and is only affected by the quadrupole pathway. The results are supported by the relevant parameters (hyperfine and quadrupole coupling constants) calculated by relativistic DFT methods. This finding opens up new avenues for investigating the structure and reactivity of paramagnetic GdIII complexes used as contrast agents in magnetic resonance imaging.

lanthanide complexesLanthanideGadoliniumchemistry.chemical_elementImaging agentsCatalysisNMR spectroscopy; Density functional calculations; lanthanide complexes; gadolinium; O-17 nmrParamagnetismchemistry.chemical_compoundNMR spectroscopyNuclear magnetic resonanceLanthanidesDOTAHyperfine structureChemistryOrganic ChemistryRelaxation (NMR)General ChemistryNuclear magnetic resonance spectroscopyDensity functional calculationsSettore CHIM/03 - Chimica Generale E InorganicaQuadrupole17O NMR Lanthanides DFTCondensed Matter::Strongly Correlated ElectronsgadoliniumO-17 nmr
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Efficient Conversion of Carbon Dioxide by Imidazolium-Based Cross-Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Buildi…

2019

Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular building blocks for the synthesis of imidazolium cross-linked networks, to be used as heterogeneous catalysts for the conversion of carbon dioxide into cyclic carbonates. Two hybrid materials with different nucleophilic species (bromide and iodide) have been prepared and characterized by means of elemental analysis, 13C and 29Si solid-state NMR spectroscopy, thermogravimetric analysis and IR spectroscopy. The solids were tested as the sole catalyst under metal- and solvent-free reaction conditions showing full selectivity toward the formation of cyclic carbonates. High turnover number (TON) and productivity values,…

Thermogravimetric analysisMaterials science010405 organic chemistryGlycidolInfrared spectroscopypolyhedral oligomeric silsesquioxanesGeneral Chemistrycyclic carbonatesimidazolium salts010402 general chemistryHeterogeneous catalysis01 natural sciencesSilsesquioxane0104 chemical sciencesCatalysischemistry.chemical_compoundcarbon dioxide conversioncyclic carbonateheterogeneous catalysischemistryChemical engineeringheterogeneous catalysiMoietyHybrid materialimidazolium salt
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Selective recognition of neutral guests in an aqueous medium by a biomimetic calix[6]cryptamide receptor

2015

The design of artificial receptors that can efficiently work in water is a challenging research area. A possible biomimetic approach for the elaboration of such receptors consists of associating a hydrophobic cavity with a polar polyfunctional binding site. On this basis, a hydrophilic calix[6]cryptamide decorated with oligo(ethylene glycol) units (i.e. 8) was synthesized through an efficient [1 + 1] macrocyclization reaction as the key-step. The complexation of neutral molecules was evaluated by NMR spectroscopy through competition experiments either in apolar or aqueous media. In both media, host 8 can bind neutral species that display H-bonding acceptor and donor groups such as amides or…

Models MolecularEthylene GlycolMagnetic Resonance SpectroscopyStereochemistryAllosteric regulationMolecular ConformationCrystallography X-Ray010402 general chemistry01 natural sciencesBiochemistrychemistry.chemical_compoundBiomimetic MaterialsCalixareneUreaMoleculeaqueous mediumartificial receptorsbiomimeticsPhysical and Theoretical ChemistryBinding siteta116010405 organic chemistryHydrogen bondOrganic ChemistryWaterHydrogen BondingNuclear magnetic resonance spectroscopyAmidesAcceptor0104 chemical scienceschemistryCyclizationCalixarenesHydrophobic and Hydrophilic InteractionsEthylene glycolOrganic & Biomolecular Chemistry
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A polyhedral oligomeric silsesquioxane-based catalyst for the efficient synthesis of cyclic carbonates

2015

Polyhedral oligomeric silsesquioxane functionalized with imidazolium chloride peripheries (POSS-Imi) was successfully synthesized through a novel synthesis protocol. The solid was extensively characterized via1H NMR, 13C NMR and IR spectroscopy as well as combustion chemical analysis, mass spectrometry and transmission electron microscopy. Moreover, an in-depth investigation through 29Si NMR was performed. POSS-Imi was used for the first time as a catalyst for the conversion of CO2 and epoxides into cyclic carbonates with excellent results in terms of both yield and selectivity. The catalyst displayed improved catalytic performance with respect to unsupported 1-butyl-3-methylimidazolium chl…

Inorganic chemistryInfrared spectroscopySettore CHIM/06 - Chimica OrganicaCarbon-13 NMRsilsesquioxaneCyclic CarbonateMass spectrometryChlorideCatalysisSilsesquioxaneIonic LiquidCatalysisCatalysichemistry.chemical_compoundchemistryYield (chemistry)Polymer chemistrymedicineSelectivitymedicine.drug
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Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self-Assemble in the Presence of Europium(III) Ions: Reversible t…

2020

[EN] Hybrid nanostructures with switchable and reversible "blue-red-green" emission were efficiently synthesized. These nanostructures comprise polyhedral oligomeric silsesquioxanes (POSS) that behave as a nanocage that can be functionalized with terpyridine-based organic ligands, which can be easily complexed with europium (III) ions. The complexes were characterized by UV-Vis and fluorescence spectroscopy and their stoichiometry was also confirmed by H-1 NMR spectroscopy. In the presence of the Eu(III) ions, the octafunctionalized nanocages self-assemble to form 3D architectures that display an intense red-emission, especially in the solid state. The presence of an alkenyl group bridging …

IsomerizationNanostructureMaterials scienceLuminescenceSilsesquioxanesSelf assemblechemistry.chemical_element010402 general chemistry01 natural sciencesisomerizationIonchemistry.chemical_compoundQUIMICA ORGANICAEuropiumPolymer chemistryluminescenceeuropium010405 organic chemistryself-assemblyGeneral ChemistrySelf-assemblySilsesquioxane0104 chemical sciencessilsesquioxaneschemistrySelf-assemblyLuminescenceEuropiumIsomerization
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Polyhedral Oligomeric Silsesquioxane Based Catalyst for the Efficient Synthesis of Cyclic Carbonates

2015

In this work, the synthesis of a novel imidazolium-based polyhedral oligomeric silsesquioxane (POSS-mim-Cl) material is presented. The new nanometer-size organosilica based compound was employed for chemical fixation of CO2 into epoxide under homogeneous conditions. The target reaction was represented by the obtention of cyclic carbonates starting from epoxides and CO2. Particularly, styrene oxide was chosen as reference substrate. In addition, different parameters (solvent, temperature, pressure of CO2, and mass of the catalyst) were modified to find the best condition for CO2 conversion. The catalyst POSS-mim-Cl displayed good catalytic performances, the best results being obtained at 40 …

Ionic Liquids POSSCatalysis Polyhedral Oligomeric Silsesquioxane Conversion of CO2 Cyclic CarbonatesSettore CHIM/06 - Chimica OrganicaHomogeneous Catalysi
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Modified Carbon Nanoforms Systems for Asymmetric Catalysis

BisoxazolineFullereneCatalysi
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CCDC 1428619: Experimental Crystal Structure Determination

2015

Related Article: Angélique Lascaux, Gaël De Leener, Luca Fusaro, Filip Topić, Kari Rissanen, Michel Luhmer, Ivan Jabin|2016|Org.Biomol.Chem.|14|738|doi:10.1039/C5OB02067K

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates3915354156-hexa-t-butyl-526061-trimethoxy-193146-trioxa-22252849-tetraazanonacyclo[23.19.7.71733.1711.13943.15458.0545.01318.03237]henhexaconta-1(45)247(60)81013151732343639(52)404254(61)5557-octadecaene-232750-trione calix[6]cryptamide imidazolidin-2-one chloroform diisopropyl ether solvate
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CCDC 1428618: Experimental Crystal Structure Determination

2015

Related Article: Angélique Lascaux, Gaël De Leener, Luca Fusaro, Filip Topić, Kari Rissanen, Michel Luhmer, Ivan Jabin|2016|Org.Biomol.Chem.|14|738|doi:10.1039/C5OB02067K

Space GroupCrystallographyCrystal SystemCrystal Structure3915354156-hexa-t-butyl-526061-trimethoxy-193146-trioxa-22252849-tetraazanonacyclo[23.19.7.71733.1711.13943.15458.0545.01318.03237]henhexaconta-1(45)247(60)81013151732343639(52)404254(61)5557-octadecaene-232750-trione calix[6]cryptamide imidazolidin-2-one chloroform pentane solvateCell ParametersExperimental 3D Coordinates
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