Search results for " Bases"

showing 10 items of 272 documents

Selective Implantation of Diamines for Cooperative Catalysis in Isoreticular Heterometallic Titanium–Organic Frameworks

2021

[EN] We introduce the first example of isoreticular titanium-organic frameworks, MUV-10 and MUV-12, to show how the different affinity of hard Ti(IV) and soft Ca(II) metal sites can be used to direct selective grafting of amines. This enables the combination of Lewis acid titanium centers and available -NH, sites in two sizeable pores for cooperative cycloaddition of CO2 to epoxides at room temperature and atmospheric pressure. The selective grafting of molecules to heterometallic clusters adds up to the pool of methodologies available for controlling the positioning and distribution of chemical functions in precise positions of the framework required for definitive control of pore chemistr…

Materials science010405 organic chemistrychemistry.chemical_elementGeneral ChemistryGeneral MedicineGrafting010402 general chemistryCombinatorial chemistry01 natural sciencesCatalysisCycloadditionCatalysis0104 chemical sciencesMetalchemistryvisual_artvisual_art.visual_art_mediumMoleculeLewis acids and basesTitaniumAngewandte Chemie International Edition
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Calculations on solvents and co-solvents of single-wall carbon nanotubes: Cyclopyranoses

2005

Abstract (10,10) single-wall carbon nanotube (SWNT) presents consistency between relatively small solubility, and great partition coefficients and kinetic stability. Solubility of SWNTs is investigated in a variety of solvents, finding a class of non-hydrogen-bonding Lewis bases that provides good solubility. Electron affinity of d -glucopyranoses ( d -Glcpn) suggests colloids of negatively charged SWNTs in water.

Materials scienceCarbon nanotubeCondensed Matter PhysicsKinetic energyBiochemistryInclusion compoundlaw.inventionPartition coefficientchemistry.chemical_compoundColloidchemistryChemical engineeringlawElectron affinityOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistrySolubilityCo solventJournal of Molecular Structure: THEOCHEM
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Structural and optical properties of Fe and Zn substituted CuInS2 nanoparticles synthesized by a one-pot facile method

2015

We substitute indium present in the CuInS2 ternary compound by iron and zinc using a facile one-pot synthesis method. The quaternary compound of CuIn1−xMxS2 (M = Fe and Zn) was synthesized by dissolving CuCl, InCl3, FeCl3, Zn(ac)2 and SC(NH2)2 as precursors in 1-octadecene, oleylamine and oleic acid as non-coordinating, coordinating and capping agent solvents, respectively. Oleic acid, oleylamine and thiourea were used respectively as a hard Lewis base, borderline Lewis base (in comparison with oleic acid) and soft Lewis base to form appropriate complexes. The complex formation, structure, and optical properties of CuIn1−xMxS2 (M = Fe and Zn) nanoparticles were studied by Fourier transform …

Materials scienceInorganic chemistrychemistry.chemical_elementGeneral ChemistryZincchemistry.chemical_compoundchemistryThioureaX-ray photoelectron spectroscopyTernary compoundOleylamineMaterials ChemistryLewis acids and basesFourier transform infrared spectroscopySpectroscopyJournal of Materials Chemistry C
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Nanorings and rods interconnected by self-assembly mimicking an artificial network of neurons

2013

[EN] Molecular electronics based on structures ordered as neural networks emerges as the next evolutionary milestone in the construction of nanodevices with unprecedented applications. However, the straightforward formation of geometrically defined and interconnected nanostructures is crucial for the production of electronic circuitry nanoequivalents. Here we report on the molecularly fine-tuned self-assembly of tetrakis-Schiff base compounds into nanosized rings interconnected by unusually large nanorods providing a set of connections that mimic a biological network of neurons. The networks are produced through self-assembly resulting from the molecular conformation and noncovalent intermo…

Materials scienceNanostructurePolymersSurface PropertiesEvaporationGeneral Physics and AstronomyNanoparticleNanotechnologyElectronsHardware_PERFORMANCEANDRELIABILITY010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyRodCircuitsCIENCIA DE LOS MATERIALES E INGENIERIA METALURGICAHardware_INTEGRATEDCIRCUITSAnimalsHumansNanotechnologyMolecular circuitsRingsSchiff BasesElectronic circuitNeuronsMultidisciplinaryNanotubes010405 organic chemistryFlowElectric ConductivityArchitecturesGeneral ChemistryEvaporation (deposition)0104 chemical sciencesNanostructuresNanoparticlesSelf-assemblyNeural Networks ComputerPrinciplesHardware_LOGICDESIGNModel
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Synthesis, photophysical properties and structures of organotin-Schiff bases utilizing aromatic amino acid from the chiral pool and evaluation of the…

2017

Abstract Five new organotin(IV) complexes of compositions [Me 2 SnL 1 ] ( 1 ), [Me 2 SnL 2 ] n ( 2 ), [Me 2 SnL 3 ] ( 3 ), [Ph 3 SnL 1 H] n ( 4 ) and [Ph 3 SnL 3 H] ( 5 ) (where L 1  = (2 S )-2-(( E )-(( Z )-4-hydroxypent-3-en-2-ylidene)amino)-3-(1 H -indol-3-yl)propanoate, L 2  = (2 S )-( E )-2-((2-hydroxybenzylidene)amino)-3-(1 H -indol-3-yl)propanoate and L 3  = (2 S )-( E )-2-((1-(2-hydroxyphenyl)ethylidene)amino)-3-(1 H -indol-3-yl)propanoate were synthesized and spectroscopically characterized. The crystal structures of 1 – 4 were determined. For the dimethyltin derivative 2 , a polymeric chain structure was observed as a result of a long Sn∙∙∙O contact involving the exocyclic carbony…

Models MolecularCell SurvivalStereochemistryAntineoplastic AgentsCrystal structureChiral Schiff baseCrystallography X-Ray010402 general chemistry01 natural sciencesBiochemistryInorganic ChemistryAmino Acids AromaticInhibitory Concentration 50chemistry.chemical_compoundBromideCell Line TumorRiboseOrganotin CompoundsHumansSchiff BasesSpectroscopyX-ray crystallographyCoordination geometrychemistry.chemical_classificationCyclodextrin010405 organic chemistryLigandA375 (human melanoma) cell lineTryptophanStereoisomerismPhotochemical ProcessesOrganotin(IV) compound0104 chemical sciencesMolecular Docking SimulationMonomerchemistrySettore CHIM/03 - Chimica Generale E InorganicaDerivative (chemistry)Journal of Inorganic Biochemistry
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G-quadruplex vs. duplex-DNA binding of nickel(II) and zinc(II) Schiff base complexes

2016

Novel nickel(II) (1) and zinc(II) (2) complexes of a Salen-like ligand, carrying a pyrimidine ring on the N,N' bridge, were synthesized and characterized. Their interaction with duplex and G-quadruplex DNA was investigated in aqueous solution through UV-visible absorption, circular dichroism and viscometry measurements. The results obtained point out that, while the zinc(II) complex does not interact with both duplex and G-quadruplex DNA, the nickel(II) complex 1 binds preferentially to G-quadruplex respect to duplex-DNA, with values of the DNA-binding constants, Kb, 2.6×10(5)M(-1) and 3.5×10(4)M(-1), respectively. Molecular dynamics simulations provided an atomic level model of the top-sta…

Models MolecularCircular dichroismComputational chemistryInorganic chemistryBinding constantchemistry.chemical_elementZincCircular dichroism010402 general chemistryG-quadruplexDNA G-quadruplex nickel01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundNickelheterocyclic compoundsSchiff BasesSchiff base010405 organic chemistryOligonucleotidezincDNABinding constantSettore CHIM/08 - Chimica Farmaceutica0104 chemical sciencesG-QuadruplexesCrystallographyNickelchemistryDuplex (building)Settore CHIM/03 - Chimica Generale E Inorganica
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A Molecular Electron Density Theory Study of the Competitiveness of Polar Diels–Alder and Polar Alder-ene Reactions

2018

Indexación: Scopus. Funding: Ministry of Economy and Competitiveness (MINECO) of the Spanish Government, project CTQ2016-78669-P (AEI/FEDER, UE) and Fondecyt (Chile) grant 1180348. Acknowledgments: This research was supported by the Ministry of Economy and Competitiveness (MINECO) of the Spanish Government, project CTQ2016-78669-P (AEI/FEDER, UE) and Fondecyt (Chile) grant 1180348. L.R.D. thanks Fondecyt for continuous support through Cooperación Internacional. M.R.-G. also thanks MINECO for a post-doctoral contract cofinanced by the European Social Fund (BES-2014-068258). The competitiveness of the BF3 Lewis acid (LA) catalyzed polar Diels–Alder (P-DA) and polar Alder-ene (P-AE) reactions …

Models MolecularDienePharmaceutical Science01 natural sciencesAnalytical ChemistryDioxanesAlder-ene reactionschemistry.chemical_compoundComputational chemistryDrug DiscoverySingle bondLewis acids and basesBoranesLewis AcidsCycloaddition ReactionChemistryStereoisomerismPrins reactionMolecular Electron Density Theory Diels-Alder reactionsChemistry (miscellaneous)ElectrophileThermodynamicsMolecular Medicinecompetitive reactionscompetitive reactions polar reactionsAllylic rearrangementElectrons010402 general chemistryArticleCatalysislcsh:QD241-441lcsh:Organic chemistryPseudocyclic selectivityFormaldehydeButadienespolar reactionsPhysical and Theoretical ChemistryEne reactionDiels-Alder reactionsPrins reaction pseudocyclic selectivity010405 organic chemistryOrganic ChemistryMolecular Electron Density TheoryPolar reactionsPhenanthrenespseudocyclic selectivity0104 chemical sciencesPrins reactionQuantum TheoryCompetitive reactionsMolecules
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Dihydrogen Activation by Antiaromatic Pentaarylboroles

2010

Facile metal-free splitting of molecular hydrogen (H(2)) is crucial for the utilization of H(2) without the need for toxic transition-metal-based catalysts. Frustrated Lewis pairs (FLPs) are a new class of hydrogen activators wherein interactions with both a Lewis acid and a Lewis base heterolytically disrupt the hydrogen-hydrogen bond. Here we describe the activation of hydrogen exclusively by a boron-based Lewis acid, perfluoropentaphenylborole. This antiaromatic compound reacts extremely rapidly with H(2) in both solution and the solid state to yield boracyclopent-3-ene products resulting from addition of hydrogen atoms to the carbons alpha to boron in the starting borole. The disruption…

Models MolecularHydrogenHydrogen bondchemistry.chemical_elementHydrogen BondingGeneral ChemistryPhotochemistryBiochemistryCatalysisFrustrated Lewis pairCatalysischemistry.chemical_compoundColloid and Surface ChemistrychemistryThermodynamicsOrganic chemistryLewis acids and basesBoroleBoronBoronHydrogenAntiaromaticityJournal of the American Chemical Society
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Stereochemical Consequences of Oxygen Atom Transfer and Electron Transfer in Imido/Oxido Molybdenum(IV, V, VI) Complexes with Two Unsymmetric Bidenta…

2012

Two equivalents of the unsymmetrical Schiff base ligand (L(tBu))(-) (4-tert-butyl phenyl(pyrrolato-2-ylmethylene)amine) and MoCl(2)(NtBu)O(dme) (dme = 1,2-dimethoxyethane) gave a single stereoisomer of a mixed imido/oxido Mo(VI) complex 2(tBu). The stereochemistry of 2(tBu) was elucidated using X-ray diffraction, NMR spectroscopy, and DFT calculations. The complex is active in an oxygen atom transfer (OAT) reaction to trimethyl phosphane. The putative intermediate five-coordinate Mo(IV) imido complex coordinates a PMe(3) ligand, giving the six-coordinate imido phosphane Mo(IV) complex 5(tBu). The stereochemistry of 5(tBu) is different from that of 2(tBu) as shown by NMR spectroscopy, DFT ca…

Models MolecularMagnetic Resonance SpectroscopyDenticityCoordination sphereElectronsCrystallography X-RayLigandsPhotochemistryMedicinal chemistrylaw.inventionElectron TransportInorganic Chemistrychemistry.chemical_compoundElectron transferCoordination ComplexeslawMoleculeFerrous CompoundsPhysical and Theoretical ChemistryElectron paramagnetic resonanceSchiff BasesMolybdenumSchiff baseMolecular StructureLigandStereoisomerismNuclear magnetic resonance spectroscopyOxygenEthyl EtherschemistryQuantum TheoryOxidation-ReductionInorganic Chemistry
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Synthesis, characterisation and crystal structures of Schiff bases from the reaction of 4,6-O-ethylidene-β-D-glucopyranosylamine with substituted sal…

2001

Multiple chemical modifications were carried out on D-glucose to result in the corresponding Schiff bases. Such modifications performed on D-glucose not only helped in increasing the solubility of the products in nonaqueous solvents, but also restricted the anomerisation of the saccharide moiety in solution. NMR study of the products revealed the presence of the β-anomeric form of the saccharide moiety in Me2SO solution. All the compounds were characterised by analytical and spectral methods. The literature is devoid of any crystal structures of saccharide–Schiff base combinations of the type reported in this paper. The crystal structures of these molecules exhibited a tridentate, ONO bindi…

Models MolecularMagnetic Resonance SpectroscopyStereochemistryNuclear Magnetic ResonanceCyclohexane conformationStereoisomerismCrystal structureCrystallography X-RayBiochemistryHeterocyclic Compounds 2-RingAnalytical ChemistrySpectroscopy Fourier Transform InfraredCarbohydrate ConformationMoleculeMoietySolubilitySchiff BasesAldehydesGlucosamineChemistryHydrogen bondOrganic CompoundsOrganic ChemistryHydrogen BondingStereoisomerismGeneral MedicineNuclear magnetic resonance spectroscopyCrystallographyGlucoseSolubilitySpectrophotometryCrystal StructureSolventsIndraStra Global
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