Search results for "Surfaces"

showing 10 items of 2837 documents

Small Angle Neutron Scattering, X-ray Diffraction, Differential Scanning Calorimetry, and Thermogravimetry Studies to Characterize the Properties of …

2009

Nanocomposites based on laponite RD and (ethylene oxide)98(propylene oxide)67(ethylene oxide)98 (F127)triblock copolymer or poly(ethylene) glycol 2000 (PEG2000) were prepared by using the melting method. Small-angle neutron scattering and the X-ray diffraction experiments provided insights into the organization of the laponite RD dispersed in the macromolecular matrix over a wide length scale. SANS data analysis by means of a fractal law evidenced the formation of clusters of laponite RD at long correlation distance. The single laponite RD particles and the lamellar structure of F127 were described in the shorter length scale. Finally, the crystalline structure of the macromolecule was obse…

Length scaleTGAMaterials scienceEthylene oxidenanocompositepoly(ethylene oxide)poly(propylene oxide)poly(ethylene oxide)SANSXRDAnalytical chemistrypoly(ethylene)glycol 2000laponite RDNeutron scatteringSmall-angle neutron scatteringSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDSCThermogravimetrychemistry.chemical_compoundGeneral EnergyDifferential scanning calorimetrychemistryX-ray crystallographyLamellar structurePhysical and Theoretical Chemistry
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Prodrug based on halloysite delivery systems to improve the antitumor ability of methotrexate in leukemia cell lines

2021

The prodrug approach, as well as the development of specific systems able to deliver a chemotherapeutic agent in the target site, decreasing the side effects often associated with its administration, are still a challenging. In this context, both methotrexate drug molecules (MTX) and biotin ligand moieties, whose receptors are overexpressed on the surface of several cancer cells, were loaded on halloysite nanotubes (HNTs) to develop nanomaterial based on multifunctional and "smart" delivery systems. To highlight the crucial role played by biotin, carrier systems based on HNTs and MTX were also synthetized. In detail, several approaches were envisaged: i) a supramolecular interaction between…

LeukemiaNanotubesHalloysite nanotubesBiotinAntineoplastic AgentsSurfaces and InterfacesGeneral MedicineSettore CHIM/06 - Chimica OrganicaCell LineDrug delivery systemsColloid and Surface ChemistryMethotrexateSpectroscopy Fourier Transform InfraredSettore BIO/14 - FarmacologiaClayHumansProdrugsPhysical and Theoretical ChemistryLeukemia cellsProdrugBiotechnologySettore CHIM/02 - Chimica Fisica
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An unprecedented hetero-bimetallic three-dimensional spin crossover coordination polymer based on the tetrahedral [Hg(SeCN)4]2− building block

2019

[EN] Self-assembly of octahedral FeII ions, trans-1,2-bis(4-pyridyl) ethane (bpe) bridging ligands and [Hg(XCN)(4)](2-) (X = S (1), Se (2)) tetrahedral building blocks has afforded a new type of hetero-bimetallic Hg-II-Fe-II spin-crossover (SCO) 3D 6,4-connected coordination polymer (CP) formulated {Fe(bpe)[Hg(XCN)(4)]}(n). For X = S (1), the ligand field is close to the crossing point but 1 remains paramagnetic over all temperatures. In contrast, for X = Se (2) the complex undergoes complete thermal induced SCO behaviour centred at T-1/2 = 107.8 K and complete photoconversion of the low spin state into a metastable high-spin state (LIESST effect) with T-LIESST = 66.7 K. The current results…

Ligand field theoryMaterials scienceSpin statesCoordination polymerCrystal structureMagnetic-Properties010402 general chemistry01 natural sciencesCatalysisLIESSTParamagnetismchemistry.chemical_compoundSpin crossoverPressureMaterials ChemistrySpectroscopic investigationsPolynuclear complexesCrystal-StructureBehavior010405 organic chemistryMetals and AlloysGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyOctahedronchemistryFISICA APLICADATransitionX-RayCeramics and CompositesHg(Scn)(4)(2-) UnitStateChemical Communications
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Factors affecting copper(II) binding to multiarmed cyclam-grafted mesoporous silica in aqueous solution

2009

Single- as well as multi-anchored cyclam-functionalized silica samples have been prepared by grafting amorphous silica gel (K60) and mesostructured silica (SBA-15) with silylated cyclam precursors bearing one, two, or four triethoxysilyl groups, respectively ascribed to cyclam-mono, cyclam-di, and cyclam-tetra. Their reactivity toward copper(II) has been thoroughly investigated in aqueous solution and discussed with respect to the number of arms tethering the ligand to the silica surface and the structural ordering of the adsorbent in terms of capacity, long-term stability, and speed of access to the binding sites. Less-than-complete metal ion uptake was always observed, even in excess of c…

Ligand field theoryStereochemistrychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundCyclamPolymer chemistryElectrochemistryGeneral Materials ScienceReactivity (chemistry)SpectroscopyAlkylComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationAqueous solutionSilica gelSurfaces and Interfaces[CHIM.MATE]Chemical Sciences/Material chemistryMesoporous silica021001 nanoscience & nanotechnologyCondensed Matter PhysicsCopper0104 chemical scienceschemistry[ CHIM.MATE ] Chemical Sciences/Material chemistry0210 nano-technology
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Harvesting Fluorescence from Efficient Tk -> Sj (j, k > 1) Reverse Intersystem Crossing for ??* Emissive Transition-Metal Complexes

2013

Using a bimetallic Au(I) complex bearing alkynyl-(phenylene)3-diphosphine ligand (A-3), we demonstrate that the fluorescence can be exquisitely harvested upon T1 → Tk (k > 1) excitation followed by Tk → Sj (j, k > 1) intersystem crossing (ISC) back to the S1 state. Upon S0 → S1 355 nm excitation, the S1 → T1 intersystem crossing rate has been determined to be 8.9 × 108 s–1. Subsequently, in a two-step laser pump–probe experiment, following a 355 nm laser excitation, the 532 nm T1 → Tk probing gives the prominent blue 375 nm fluorescence, and this time-dependent pump–probe signal correlates well with the lifetime of the T1 state. Careful examination reveals the efficiency of Tk → Sj (j, k > …

LigandChemistryPhotochemistryInternal conversion (chemistry)FluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyIntersystem crossingTransition metalPhenylenePhysical and Theoretical ChemistryPhosphorescenceta116ExcitationThe Journal of Physical Chemistry C
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More electron rich than cyclopentadienyl: 1,2-diaza-3,5-diborolyl as a ligand in ferrocene and ruthenocene analogs

2011

Ruthenium and iron sandwich complexes incorporating cyclopentadienyl analogs with CB(2)N(2)(-) skeletons were characterized. Electrochemical measurements supported by computational studies revealed that in combination with larger metal ions such as Ru the CB(2)N(2)(-) ligand can be more electron-rich than its organic counterpart.

LigandMetal ions in aqueous solutionMetals and Alloyschemistry.chemical_elementGeneral ChemistryElectronPhotochemistryElectrochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRutheniumchemistry.chemical_compoundCyclopentadienyl complexFerrocenechemistryPolymer chemistryMaterials ChemistryCeramics and CompositesRuthenoceneta116Chemical Communications
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Monitoring Thiol–Ligand Exchange on Au Nanoparticle Surfaces

2018

Surface functionalization of nanoparticles (NPs) plays a crucial role in particle solubility and reactivity. It is vital for particle nucleation and growth as well as for catalysis. This raises the quest for functionalization efficiency and new approaches to probe the degree of surface coverage. We present an (in situ) proton nuclear magnetic resonance (1H NMR) study on the ligand exchange of oleylamine by 1-octadecanethiol as a function of the particle size and repeated functionalization on Au NPs. Ligand exchange is an equilibrium reaction associated with Nernst distribution, which often leads to incomplete surface functionalization following “standard” literature protocols. Here, we show…

LigandNanoparticle02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundsymbols.namesakechemistryOleylamineElectrochemistryProton NMRsymbolsSurface modificationGeneral Materials ScienceReactivity (chemistry)Nernst equationParticle size0210 nano-technologySpectroscopyLangmuir
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A dinucleating ligand which promotes DNA cleavage with one and without a transition metal ion.

2013

The dinucleating ligand L (1,3-bis[bis(pyridin-2-ylmethyl)amino]propan-2-ol) combined with metal ions efficiently cleaves DNA when M : L is 1 : 1 (M = Co(II) or Fe(III)) at pH 5.5–7.0, with free L being more active at acidic pH than when bound to Zn(II), Cu(II) or Ni(II) at neutral pH.

LigandPyridinesMetal ions in aqueous solutionInorganic chemistryMetals and AlloysGeneral ChemistryDNALigandsTransition metal ionsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryDna cleavageCoordination ComplexesPolymer chemistryMaterials ChemistryCeramics and CompositesTransition ElementsNeutral phDNA CleavageDNAPlasmidsChemical communications (Cambridge, England)
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A non-heme dinuclear iron(II) complex containing a single, unsupported hydroxo bridge.

2006

Complexation of the tetrapodal pentadentate NN4 ligand 2,6-C5H3N[CMe(CH2NH2)2]2 (I) with iron(II) perchlorate hydrate in methanol, in the presence of N-methylimidazole, produces a diferrous complex with a single, unsupported mu-OH ligand between two {(I)FeII} coordination modules.

LigandStereochemistryMetals and AlloysGeneral ChemistryBridge (interpersonal)CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPerchloratechemistry.chemical_compoundCrystallographychemistryMaterials ChemistryCeramics and CompositesNon hemeMethanolHydrateChemical communications (Cambridge, England)
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Multielectron oxidation in a ferromagnetically coupled dinickel(ii) triple mesocate.

2015

Triple-stranded dinuclear nickel(ii) complexes of the meso-helicate type have been obtained from the new N,N'-1,3-phenylenebis(pyrazine-2-carboxamidate) ligand; they possess a multielectron redox behaviour featuring up to four stepwise, one-electron oxidation reactions of the two ferromagnetically coupled Ni(II) ions to afford the putative high-valent dinickel(iii) and dinickel(iv) species, as supported by theoretical calculations.

LigandStereochemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryRedoxCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonNickelCrystallographychemistryMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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