Search results for "Bromide"

showing 10 items of 591 documents

Copper(I) Bromide: An Alternative Emitter for Blue-Colored Flame Pyrotechnics.

2015

Copper(I) bromide was evaluated as an alternative emitter for blue flame pyrotechnic compositions. CuBr and CuCl emission spectra were recorded from a butane torch flame and compared. Cu(BrO3 )2 was synthesized and used in pyrotechnic compositions as an oxidizer and the source for the generation of CuBr species. Pyrotechnic compositions, which contained copper and potassium bromates as oxidizers, were optimized for the generation of blue flames. The experimental data, including emission spectra of the flames, chromaticity coordinates, burning rates, luminous intensities, and sensitivity tests, were analyzed and compared.

Organic ChemistryAnalytical chemistryPyrotechnicschemistry.chemical_elementCopper(I) bromideNanotechnologyButaneGeneral ChemistryCopperCatalysischemistry.chemical_compoundBlue coloredchemistryBromideEmission spectrumChromaticityChemistry (Weinheim an der Bergstrasse, Germany)
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On the reactivity of 3-bromo-2-nitrobenzo[ b ]thiophene with nucleophiles: elucidation of the base-catalysed mechanism with rearrangement

2001

Abstract The reactivity of 3-bromo-2-nitrobenzo[b]thiophene (1) with several (anionic and neutral) nucleophiles has been examined. Only with neutral, weak nucleophiles (as anilines) 1 gives, in the presence of non-nucleophilic bases (triethylamine or potassium carbonate), together with the ‘expected’ 3-amino-2-nitrobenzo[b]thiophenes (3) also the ‘unexpected’ 2-amino-3-nitrobenzo[b]thiophenes (4). The composition of the final isomeric mixture depends on the base added (nature and quantity) and on the solvent used. The results demonstrate the relevance of base-catalysis and support a reaction pathway involving the formation of an anionic intermediate (B) which undergoes addition of a second …

Organic ChemistryBiochemistryMedicinal chemistryPotassium carbonatechemistry.chemical_compoundchemistryNucleophileBromideDrug DiscoveryNitroThiopheneMoleculeReactivity (chemistry)TriethylamineTetrahedron
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Anion–π Interactions in Salts with Polyhalide Anions: Trapping of I 4 2−

2010

The directionality of interaction of electron-deficient π systems with spherical anions (e.g,. halides) can be controlled by secondary effects like NH or CH hydrogen bonding. In this study a series of pentafluorophenyl-substituted salts with polyhalide anions is investigated. The compounds are obtained by aerobic oxidation of the corresponding halide upon crystallization. Solid-state structures reveal that in bromide 2, directing NH-anion interactions position the bromide ion in an η(1)-type fashion over but not in the center of the aromatic ring. The same directing forces are effective in corresponding tribromide salt 3. In the crystal, the bromide ion is paneled by four electron-deficient…

Organic ChemistryInorganic chemistryChemieSupramolecular chemistryHalideGeneral ChemistryCrystal structureCatalysischemistry.chemical_compoundCrystallographychemistryBromideHalogenPi interactionTriiodideTribromideChemistry – A European Journal
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Stabilisation of LDPE cross-linked in the presence of peroxidesII. FTIR study of chemical changes taking place in the LDPE–dicumyl peroxide–Irganox 1…

2000

Abstract The chemical changes taking place in the systems: LDPE–Irganox 1081, LDPE–dicumyl peroxide and LDPE–Irganox 1081–dicumyl peroxide, after homogenisation (in a rolling mill at 130°C) and after homogenisation and cross-linking (at 180°C and 5.0 MPa for 20 min) were investigated by FTIR. It was found that the OH groups in Irganox 1081 were in a bound form, and were most probably linked to the sulphur co-ordination centre. Further, the presence of dicumyl peroxide without Irganox 1081 in LDPE resulted in the formation of hydroperoxide groups at a temperature of 130°C, which were replaced by free hydroxy and carbonyl groups of a ketonic type after cross-linking. Simultaneous addition of …

Organic peroxidePolymers and PlasticsPotassium bromideConcentration effectPolyethyleneCondensed Matter PhysicsPeroxideLow-density polyethylenechemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMaterials ChemistryOrganic chemistryPartial oxidationFourier transform infrared spectroscopyPolymer Degradation and Stability
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Elemental Bromine Production by TiO2 Photocatalysis and/or Ozonation

2016

Significant production of elemental bromine (Br2 ) was observed for the first time when treating bromide containing solutions at acidic pH, with TiO2 photocatalyst, ozone, or a combination thereof. Br2 selectivities up to approximately 85 % were obtained and the corresponding bromine mass balance values satisfied. The process is general and may be applied at a laboratory scale for green bromination reactions, or industrially as a cheap, safe, and environmentally sustainable alternative to the currently applied bromine production methods.

Ozone010504 meteorology & atmospheric sciencesbromineozonationInorganic chemistrychemistry.chemical_element010501 environmental sciencesLaboratory scale010402 general chemistry01 natural sciencesCatalysisCatalysiphotocatalysichemistry.chemical_compoundNitric acidBromideTiO20105 earth and related environmental sciencesSettore ING-IND/24 - Principi Di Ingegneria ChimicaBromineChemistry (all)HalogenationTio2 photocatalystGeneral MedicineGeneral Chemistry0104 chemical sciencesnitric acidchemistryPhotocatalysisAngewandte Chemie International Edition
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Primary structure and unusual carbohydrate moiety of functional unit 2-c of keyhole limpet hemocyanin (KLH)

1999

Abstract The complete amino acid sequence of the Megathura crenulata hemocyanin functional unit KLH2-c was determined by direct sequencing and matrix-assisted laser desorption ionization mass spectrometry of the protein, and of peptides obtained by cleavage with EndoLysC proteinase, chymotrypsin and cyanogen bromide. This is the first complete primary structure of a functional unit c from a gastropod hemocyanin. KLH2-c consists of 420 amino acid residues. Circular dichroism spectra indicated approx. 31% β-sheet and 29% α-helix contents. A multiple sequence alignment with other molluscan hemocyanin functional units revealed average identities between 41 and 49%, but 55% in case of Octopus he…

Peanut agglutininmedicine.medical_treatmentMolecular Sequence DataCarbohydratesBiophysicschemical and pharmacologic phenomenaMegathura crenulataBiochemistrychemistry.chemical_compoundStructural BiologymedicineAnimalsChymotrypsinAmino Acid SequenceRNA MessengerMolecular BiologyPeptide sequenceChromatography High Pressure LiquidbiologyMolecular massCircular DichroismProtein primary structureHemocyaninbiology.organism_classificationMolecular WeightBiochemistrychemistryMolluscaSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationHemocyaninsbiology.proteinElectrophoresis Polyacrylamide GelCyanogen bromideSequence AlignmentKeyhole limpet hemocyaninBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology
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Chiroptical Phenomena in Reverse Micelles: The Case of (1R,2S)-Dodecyl (2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium Bromide (DMEB)

2014

(1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB) aggregates dispersed in carbon tetrachloride have been investigated by Fourier transform infrared (FT-IR), vibrational circular dichroism (VCD) and 1H nuclear magnetic resonance (NMR) spectroscopy at various surfactant concentration and water-to-surfactant molar ratio. Experimental data indicate that, even at the lowest investigated concentration and in absence of added water, DMEB molecules associate in supramolecular assemblies. At higher DMEB concentration the aggregates can confine water molecules, making it plausible to think that DMEB form reverse micelles and that water molecules are quite uniformly dist…

PharmacologyHydrogen bondOrganic ChemistrySupramolecular chemistryPhotochemistryMicelleCatalysisAnalytical Chemistrychemistry.chemical_compoundchemistryBromideDrug DiscoveryVibrational circular dichroismProton NMRMoleculeOrganic chemistryChirality (chemistry)SpectroscopyChirality
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Preparation of Carbon-14 Labeled 2-(2-mercaptoacetamido)-3-phenylpropanoic Acid as Metallo-beta-lactamases Inhibitor (MBLI), for Coadministration wit…

2019

Aim and Objective: Bacteria could become resistant to β-lactam antibiotics through production of β- lactamase enzymes like metallo-β-lactamase. 2-(2-mercaptoacetamido)-3-phenylpropanoic acid was reported as a model inhibitor for this enzyme. In order to elucidate the mechanism of action in the body’s internal environment, preparation of a labeled version of 2-(2-mercaptoacetamido)-3-phenylpropanoic acid finds importance. In this regard, we report a convenient synthetic pathway for preparation of carbon-14 labeled 2-(2- mercaptoacetamido)-3-phenylpropanoic acid. Materials and Methods: This study was initiated by using non-radioactive materials. Then, necessary characterization was performed…

Phenylpropionates010405 organic chemistryHydrochlorideOrganic ChemistryPhenylalanine02 engineering and technology021001 nanoscience & nanotechnologybeta-Lactams01 natural sciencesBiochemistry0104 chemical sciencesAnti-Bacterial Agentschemistry.chemical_compoundAcetic acidIsoelectric pointBenzyl bromidechemistryYield (chemistry)Peptide bondCarbon Radioisotopes0210 nano-technologyThioacetic acidbeta-Lactamase InhibitorsNuclear chemistryCurrent organic synthesis
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Tunable luminescent lead bromide complexes

2020

Lead halides are used extensively to prepare perovskite-based devices but it is less known that lead halides can also form luminescent complexes in solvents. Using polyethylene glycol as a solvent, a lead bromide complex with a photoluminescence quantum yield over 20% is obtained and the photoluminescence peak can be shifted around 50 nm with different alkylammonium bromides.

PhotoluminescenceMaterials scienceInorganic chemistryLead bromideQuantum yieldHalideGeneral ChemistryPolyethylene glycolSolventchemistry.chemical_compoundchemistryMaterials ChemistryLuminescenceMaterialsCèl·lules fotoelèctriquesPerovskite (structure)
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The Luminescence of CH3NH3PbBr3Perovskite Nanoparticles Crests the Summit and Their Photostability under Wet Conditions is Enhanced

2016

CH3 NH3 PbBr3 perovskite nanoparticles (PAD ) are prepared with a photoluminescence quantum yield of ≈100% in air atmosphere by using the quasi-spherical shaped 2-adamantylammonium bromide (ADBr) as the only capping ligand. The photostability under wet conditions of this kind of nanoparticles is enhanced by using cucurbit[7]uril-adamantylammonium (AD@CB) host-guest complexes as the capping ligand.

PhotoluminescenceMaterials scienceLigandInorganic chemistryNanoparticleQuantum yield02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesBiomaterialschemistry.chemical_compoundchemistryBromideCucurbiturilGeneral Materials Science0210 nano-technologyLuminescenceBiotechnologyPerovskite (structure)Small
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