Search results for "boron"

showing 10 items of 352 documents

A DFT study for the regioselective 1,3-dipolar cycloadditions of nitrile N-oxides toward alkynylboronates

2003

Abstract The mechanism for the 1,3-dipolar cycloaddition of benzonitrile oxide toward ethynyl and propynylboronate has been studied by using density functional theory (DFT) at B3LYP/6-31G* level. These cycloadditions are concerted [3+2] processes. The presence of the two oxygens on the boronic ester precludes the participation of the boron atom on [3+3] processes. The two regioisomeric channels associated to the formation of the isoxazoles bearing the boronic ester unit on the 4- or 5-positions have been characterized. The B3LYP/6-31G* activation parameters are in acceptable agreement with the experiments, allowing to explain the factors controlling these regioselective cycloadditions.

NitrileStereochemistryOrganic ChemistryOxideRegioselectivityBoron atomBiochemistryMedicinal chemistryCycloadditionchemistry.chemical_compoundDipoleBenzonitrilechemistryDrug DiscoveryDensity functional theoryTetrahedron
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Towards the elaboration of new gold-based optical theranostics.

2014

Four new red BODIPY–gold(I) theranostic compounds were synthesized. Some of them were vectorized by tethering a biovector (glucose or bombesin derivatives) to the metallic center. Their photophysical properties were studied. Additionally, their cytotoxicity was examined on different cancer cell lines and on a normal cell line, they were tracked in vitro by fluorescence detection, and their uptake was evaluated by ICP-MS measurements.

Boron CompoundsChemistryOptical ImagingNanotechnologyBiological TransportFluorescenceInorganic ChemistryNormal cellMicroscopy FluorescenceCell Line TumorBiophysicsOrganometallic CompoundsHumansBombesinGoldCancer cell linesCytotoxicityDalton transactions (Cambridge, England : 2003)
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Tuning the Electronic Properties of the Dative N-B Bond with Associated O-B Interaction: Electron Localizability Indicator from X-Ray Wavefunction Re…

2016

Despite the immense growth in interest in difluoroborate dyes, the nature of the interactions of the boron atom within the N-BF2 -O kernel is not yet fully understood. Herein, a set of real-space bonding indicators is used to quantify the electronic characteristics of the dative N-B bond in difluoroborate derivatives. The atoms-in-molecules (AIM) partitioning scheme is complemented by the electron localizability indicator (ELI-D) approach, and both were applied to experimental and theoretical electron-density distributions (X-ray constrained wavefunction fitting vs. DFT calculations). Additionally, Fermi orbital analysis was introduced for small DFT models to support and extend the findings…

010405 organic chemistryChemistryX-raychemistry.chemical_elementElectron010402 general chemistry01 natural sciencesQuantum chemistryAtomic and Molecular Physics and Optics0104 chemical sciencesChemical bondChemical physicsKernel (statistics)Physical and Theoretical ChemistryAtomic physicsWave functionBoronFermi Gamma-ray Space TelescopeChemphyschem : a European journal of chemical physics and physical chemistry
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Electrochemical Abatement of Organic Pollutants in Continuous-Reaction Systems through the Assembly of Microfluidic Cells in Series

2015

The electrochemical treatment of wastewater contaminated by organic pollutants was performed under a continuous mode by using, for the first time, various micro-electrochemical cells in series. A synthetic solution of acid orange 7 (AO7), a largely used azoic dye, was chosen as model wastewater. Both the electro-Fenton (EF) method with a cheap compact graphite cathode and electrochemical oxidation (EO) at a boron-doped diamond (BDD) anode were used. EO gave higher abatement of total organic carbon (TOC), but drastically higher energetic consumptions than EF. It is worth mentioning that very different operating conditions were set for EF and EO to optimize their performances. The utilization…

PollutantBoron doped diamondMaterials scienceWaste managementMicrofluidic reactorMicrofluidicsDyes/pigmentNanotechnologyElectrochemistryCatalysisOxidationElectrochemistryContinuous reactionBoron-doped diamondChemElectroChem
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Investigation of fungicidal activity of 3-piperazine-bis(benzoxaborole) and its boronic acid analogue

2014

3-Piperazine-bis(benzoxaborole) and its bis(phenylboronic acid) analogue were investigated in terms of their fungicidal activity. The study was carried out against five filamentous fungi: Aspergillus terreus, Fusarium dimerum, Fusarium solani, Penicillium ochrochloron and Aspergillus niger. 3-Piperazine-bis(benzoxaborole) revealed higher inhibitory activity towards the examined strains than standard antibiotic (amphotericin B), whereas bis(phenylboronic acid) proved to be inactive. The study unequivocally showed that the presence of the heterocyclic benzoxaborole system is essential for antifungal action of the examined compounds.

fungicidal activitybenzoxaborolesboronic acidsfungicidesApplied Organometallic Chemistry
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Fluorescent Boron Oxide Nanodisks as Biocompatible Multi-messenger Sensors for Ultrasensitive Ni$^{2+}$ Detection

2023

Boron-based nanocomposites are very promising for a wide range of technological applications, spanning from microelectronics to nanomedicine. A large variety of B-based nanomaterials has been already observed, such as borospherene, B nanotubes and nanoparticles, and boron nitride nanoparticles. However, their fabrication usually involves toxic precursors or leads to very low yields or small boron atom concentration. In this work, we report the synthesis of nanometric B$_{2}$O$_{3}$ nanodisks, a family of nanomaterials with a quasi-2D morphology capable of intense fluorescence in the visible range. Such as boron-based nanomaterial, which we synthesized by pulsed laser ablation of a boron tar…

boron oxide boron nanocomposites nanosensors nickel detection multi-messenger sensorSettore FIS/01 - Fisica Sperimentaleddc:500NATURAL sciences & mathematics
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A reliable procedure for the preparation of graphene-boron nitride superlattices as large area (cm x cm) films on arbitrary substrates or powders (gr…

2019

[EN] Herein, a reliable procedure for the preparation of graphene-boron nitride superlattices, either as films or powders, consisting of the pyrolysis at 900 degrees C of polystyrene embedded pre-formed boron nitride single sheets is reported. The procedure can serve to prepare large area films (cm x cm) of this superlattice on quartz, copper foil and ceramics. Selected area electron diffraction patterns at every location on the films show the occurrence of the graphene-boron nitride superlattice all over the film. The procedure can also be applied to the preparation of powdered samples on a gram scale. Comparison with other materials indicates that the superlattice appears spontaneously as…

Materials scienceGrapheneSuperlattice02 engineering and technologyNitride010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundQUIMICA ORGANICAchemistryElectrical resistance and conductancelawBoron nitridevisual_artvisual_art.visual_art_mediumGeneral Materials SciencePolystyreneCeramicComposite materialSelected area diffraction0210 nano-technology
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High-Mobility, Wet-Transferred Graphene Grown by Chemical Vapor Deposition

2019

We report high room-temperature mobility in single layer graphene grown by Chemical Vapor Deposition (CVD) after wet transfer on SiO$_2$ and hexagonal boron nitride (hBN) encapsulation. By removing contaminations trapped at the interfaces between single-crystal graphene and hBN, we achieve mobilities up to$\sim70000cm^2 V^{-1} s^{-1}$ at room temperature and$\sim120000cm^2 V^{-1} s^{-1}$ at 9K. These are over twice those of previous wet transferred graphene and comparable to samples prepared by dry transfer. We also investigate the combined approach of thermal annealing and encapsulation in polycrystalline graphene, achieving room temperature mobilities$\sim30000 cm^2 V^{-1} s^{-1}$. These …

Materials scienceFOS: Physical sciencesGeneral Physics and AstronomyHexagonal boron nitride02 engineering and technologyChemical vapor deposition010402 general chemistrySettore ING-INF/01 - Elettronica01 natural scienceslaw.inventionlawMesoscale and Nanoscale Physics (cond-mat.mes-hall)General Materials ScienceDry transferCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale PhysicsCharge carrier mobilityGrapheneSettore FIS/01 - Fisica Sperimentalecharge carrier mobilitygrapheneGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)HeterojunctionheterostructureCVD021001 nanoscience & nanotechnologyCombined approach0104 chemical sciencesheterostructuresChemical engineeringCrystallitecharge carrier mobility; CVD; graphene; heterostructures; transfer;0210 nano-technologytransferACS Nano
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Boron functionalization of BODIPY by various alcohols and phenols.

2013

The synthesis of new B–O BODIPY derivatives functionalized with different alkoxy or diarylalkoxy derivatives is described. These compounds were synthesized from the reaction of different B–F BODIPY precursors with various alcohols and phenols, in the presence of AlCl3. Water-soluble dyes could be synthesized as well with this method, specifically by the introduction of polyethyleneglycol (PEG) groups. A photophysical study of the different compounds was performed, and showed that the B–O BODIPY derivatives exhibit rich fluorescence properties. Finally, the conjugation of the BODIPY core has been extended using two distyryl groups, hence providing NIR emitting BODIPY derivatives, in which on…

Organic Chemistrychemistry.chemical_elementBiochemistryFluorescencechemistry.chemical_compoundchemistryPEG ratioAlkoxy groupOrganic chemistrySurface modificationPhenolsPhysical and Theoretical ChemistryBODIPYBoronOrganicbiomolecular chemistry
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5-Formyl-2-furanboronic acid at 100 K

2003

The furan ring in the title compound, C5H5BO4, is planar and each of the formyl and boronic groups makes a dihedral angle of ca 3° with this ring. The geometry of the furan ring is somewhat different to that found for substituted and unsubstituted furan structures. The mol­ecules are connected to each other in the bc plane by C—H⋯O and O—H⋯O hydrogen bonds.

chemistry.chemical_compoundchemistryHydrogen bondStereochemistryFuranGeneral Materials ScienceGeneral ChemistryDihedral angleCondensed Matter PhysicsRing (chemistry)Boronic acidActa Crystallographica Section E Structure Reports Online
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