Search results for "Halogen"

showing 10 items of 434 documents

Screening of halogenated aromatic compounds in some raw material lots for an aluminium recycling plant

2004

Four samples of scrap raw materials for an aluminium recycling plant were screened for the occurrence of persistent halogenated aromatic compounds. The samples contained waste from handling of electric and electronic plastics, filter dust from electronic crusher, cyclone dust from electronic crusher and light fluff from car shredder. In our screening analyses, brominated flame retardants were observed in all samples. Polybrominated diphenyl ethers (PBDE) were identified in all samples in amounts of 245–67450 ng/g. The major PBDE congeners found were decabromo- and pentabromodiphenyl ethers. 1,1-bis(2,4,6-tribromophenoxy)ethane, hexabromobenzene, ethyl-pentabromobenzene, tetrabromobisphenol-…

lcsh:GE1-350Conservation of Natural ResourcesWaste managementPhenyl EthersPolybrominated BiphenylsIndustrial WasteAluminium recyclingScrapRaw materialHydrocarbons AromaticHydrocarbons Brominatedchemistry.chemical_compoundPolybrominated diphenyl etherschemistryEnvironmental chemistryHexabromobenzeneHalogenated Diphenyl EthersSoil PollutantsPentabromotolueneWater Pollutants Chemicallcsh:Environmental sciencesAluminumEnvironmental MonitoringFlame RetardantsGeneral Environmental ScienceEnvironment International
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Halogens and trace metal emissions from the ongoing 2008 summit eruption of Kīlauea volcano, Hawai`i

2012

Volcanic plume samples taken in 2008 and 2009 from the Halemàumàu eruption at Kīlauea provide new insights into Kīlauea's degassing behaviour. The Cl, F and S gas systematics are consistent with syn-eruptive East Rift Zone measurements suggesting that the new Halemàumàu activity is fed by a convecting magma reservoir shallower than the main summit storage area. Comparison with degassing models suggests that plume halogen and S composition is controlled by very shallow (<3m depth) decompression degassing and progressive loss of volatiles at the surface. Compared to most other global volcanoes, Kīlauea's gases are depleted in Cl with respect to S. Similarly, our Br/S and I/S ratio measurem…

magma chamberaerosolHalideMineralogyMagma chambervolcanic eruptionchemistry.chemical_compoundGeochemistry and PetrologyemissionTrace metalaciditymercury (element)geographygeography.geographical_feature_categoryplumesolubilitydegassingparticle sizehalogenlavatrace metalSilicateAerosolPlumevolcanoVolcanochemistryEnvironmental chemistryMagmaisotopic ratioGeologyGeochimica et Cosmochimica Acta
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Melting point, molecular symmetry and aggregation of tetrachlorobenzene isomers: the role of halogen bonding

2018

Tetrachlorobenzenes represent one of the best known, but not yet fully understood, group of isomers of the structure–melting point relationship. The differences in melting temperatures of these structurally related compounds were rationalized in terms of the hierarchy and nature of formed noncovalent interactions, and the molecular aggregation that is influenced by molecular symmetry. The highest melting point is associated with the highly symmetric 1,2,4,5-tetrachlorobenzene isomer. The structures of less symmetrical 1,2,3,4-tetrachlorobenzene and 1,2,3,5-tetrachlorobenzene, determined at 270 and 90 K, show a distinct pattern of halogen bonds, characterized by the different numbers and typ…

melting pointEnthalpy02 engineering and technology010402 general chemistry01 natural sciencesGroup (periodic table)Materials ChemistryMolecular symmetryNon-covalent interactionschemistry.chemical_classificationHalogen bondstructure–property relationsIntermolecular forceMetals and Alloys021001 nanoscience & nanotechnologytetra­chloro­benzene isomersAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialsmolecular symmetryCrystallographychemistryhalogen bondingHalogenMelting point0210 nano-technologyActa Crystallographica Section B Structural Science, Crystal Engineering and Materials
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Chemoselective, Substrate-directed Fluorination of Functionalized Cyclopentane β-Amino Acids

2016

This work describes a substrate-directed fluorination of some highly functionalized cyclopentane derivatives. The cyclic products incorporating CH2 F or CHF2 moieties in their structure have been synthesized from diexo- or diendo-norbornene β-amino acids following a stereocontrolled strategy. The synthetic study was based on an oxidative transformation of the ring carbon-carbon double bond of the norbornene β-amino acids, followed by transformation of the resulted "all cis" and "trans" diformyl intermediates by fluorination with "chemodifferentiation".

molecular diversitycyclizationDouble bondHalogenationHydrocarbons FluorinatedStereochemistryMolecular Conformationchemistry.chemical_elementCyclopentanes010402 general chemistryRing (chemistry)Crystallography X-Ray01 natural sciencesBiochemistrychemistry.chemical_compoundfluorineCyclopentaneta116Norbornenechemistry.chemical_classificationamino acidssubstituent effects010405 organic chemistryOrganic ChemistrySubstrate (chemistry)StereoisomerismGeneral Chemistry0104 chemical sciencesAmino acidchemistryFluorineOxidation-ReductionChemistry: An Asian Journal
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Structures and energetic properties of 4-halobenzamides

2018

The amide bond represents one of the most fundamental functional groups in chemistry. The properties of amides are defined by amidic resonance (nN→π*C=O conjugation), which enforces planarity of the six atoms comprising the amide bond. Despite the importance of 4-halo-substituted benzamides in organic synthesis, molecular interactions and medicinal chemistry, the effect of 4-halo-substitution on the properties of the amide bond in N,N-disubstituted benzamides has not been studied. Herein, we report the crystal structures and energetic properties of a full series of 4-halobenzamides. The structures of four 4-halobenzamides (halo = iodo, bromo, chloro and fluoro) in the N-morpholinyl series h…

morpholinyl amidescrystal structure010405 organic chemistryCrystal structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)Resonance (chemistry)01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryresonance energiestwisted amidesMorpholineAmideamide bondsHalogenMaterials ChemistryPeptide bondOrganic synthesisPhysical and Theoretical ChemistryActa Crystallographica Section C Structural Chemistry
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Supramolecular Modification of ABC Triblock Terpolymers in Confinement Assembly

2018

The self-assembly of AB diblock copolymers in three-dimensional (3D) soft confinement of nanoemulsions has recently become an attractive bottom up route to prepare colloids with controlled inner morphologies. In that regard, ABC triblock terpolymers show a more complex morphological behavior and could thus give access to extensive libraries of multicompartment microparticles. However, knowledge about their self-assembly in confinement is very limited thus far. Here, we investigated the confinement assembly of polystyrene-block-poly(4-vinylpyridine)-block-poly(tert-butyl methacrylate) (PS-b-P4VP-b-PT or SVT) triblock terpolymers in nanoemulsion droplets. Depending on the block weight fractio…

nanoemulsions3D confinement assemblyMaterials scienceBlock copolymerGeneral Chemical EngineeringChemieSupramolecular chemistryNanoparticle02 engineering and technology010402 general chemistryMethacrylate01 natural sciencesArticlesupramolecular chemistrylcsh:ChemistrymulticompartmentNanoemulsionCopolymerGeneral Materials ScienceMicroparticleAlkylchemistry.chemical_classificationmicroparticlesHydrogen bond021001 nanoscience & nanotechnology0104 chemical sciencesblock copolymersLamella (surface anatomy)Microparticlelcsh:QD1-999Chemical engineeringchemistryhalogen bondSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyNanomaterials
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Four-Component Relativistic DFT Calculations of C-13 Chemical Shifts of Halogenated Natural Substances

2015

We have calculated the (13) C NMR chemical shifts of a large ensemble of halogenated organic molecules (81 molecules for a total of 250 experimental (13) C NMR data at four different levels of theory), ranging from small rigid organic compounds, used to benchmark the performance of various levels of theory, to natural substances of marine origin with conformational degrees of freedom. Carbon atoms bonded to heavy halogen atoms, particularly bromine and iodine, are known to be rather challenging when it comes to the prediction of their chemical shifts by quantum methods, due to relativistic effects. In this paper, we have applied the state-of-the-art four-component relativistic density funct…

natural productBromineChemistrynatural productsChemical shiftOrganic Chemistrychemistry.chemical_elementorganohalidesGeneral ChemistryNuclear magnetic resonance spectroscopydensity functional calculationCarbon-13 NMRhalogenCatalysisNMR spectroscopyComputational chemistryHalogendensity functional calculationshalogensMoleculeDensity functional theoryRelativistic quantum chemistrySettore CHIM/02 - Chimica Fisica
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Supramolecular Assembly of Metal Complexes by (Aryl)I⋯dz2[PtII] Halogen Bond

2020

The theoretical data for the half‐lantern complexes [Pt(C^N)(μ‐S^N)] 2 ( 1 – 3 ; С^N is cyclometalated 2‐Ph‐benzothiazole; S^N is 2‐SH‐pyridine 1 , 2‐SH‐benzoxazole 2 , 2‐SH‐tetrafluorobenzothiazole 3 ) indicate that the Pt···Pt orbital interaction leads to an increment of the nucleophilicity of the outer d z 2 ‐orbitals to provide assembly with electrophilic species. 1 – 3 were co‐crystallized with bifunctional halogen bond (XB) donors to give adducts ( 1 – 3 ) 2 ∙(1,4‐diiodotetrafluorobenzene) and infinite polymeric [ 1 ·1,1’‐diiodoperfluorodiphenyl] n . X‐ray crystallography revealed that the supramolecular assembly is achieved via (Aryl)I∙∙∙ d z 2 [Pt II ] XB between iodine σ‐holes and …

platinakemialliset sidoksetcyclometalated complexhalogen bondingsupramolekulaarinen kemiaplatinumkompleksiyhdisteetsupramolecular chemistrytheoretical calculations
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Halogen-Bonded Co-Crystals of Aromatic N-oxides : Polydentate Acceptors for Halogen and Hydrogen Bonds

2017

The C-ethyl-2-methylresorcinarene (1) forms 1:1 in-cavity complexes with aromatic N,N′-dioxides, only if each of the aromatic rings has an N−O group. The structurally different C-shaped 2,2′-bipyridine N,N′-dioxide (2,2′-BiPyNO) and the linear rod-shaped 4,4′-bipyridine N,N′-dioxide (4,4′-BiPyNO) both form 1:1 in-cavity complexes with the host resorcinarene in C4v crown and C2v conformations, respectively. In the solid state, the host–guest interactions between the 1,3-bis(4-pyridyl)propane N,N′-dioxide (BiPyPNO) and the host 1 stabilize the unfavorable anti-gauche conformation. Contrary to the N,N′-dioxide guests, the mono-N-oxide guest, 4-phenylpyridine N-oxide (4PhPyNO), does not form an…

polydentateDenticityGeneral Chemical EngineeringcooperativityInorganic chemistryCooperativity010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compounddiiodoperfluoroalkanesPyridinelcsh:QD901-999General Materials ScienceC−H···O interactionsta116hydrogen bondN−O groupHalogen bondvetysidokset010405 organic chemistryChemistryHydrogen bondH···O interactionsperfluoroalkylCondensed Matter Physicshalogen bond; hydrogen bond; aromatic N-oxides; perfluoroalkyl; diiodoperfluoroalkanes; polydentate; N−O group; cooperativity; C−H···O interactionsAcceptor0104 chemical sciencesaromatic N-oxidesCrystallographyHalogenorgaaninen kemiahalogen bondlcsh:CrystallographySingle crystalC−röntgenkristallografia
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Multifacial Recognition in Binary and Ternary Cocrystals from 5-Halouracil and Aminoazine Derivatives

2018

A systematic analysis using single crystal X-ray diffraction was performed to explore the role exerted by potential intercomponent proton-transfer reactions in the supramolecular structures of A–B cocrystals formed by 5-haloderivatives of uracil (A), coupled with 2-aminoadenine simulants (aminoazines, B). Twelve new heterodimers were synthesized in different stoichiometries and cocrystallized by solvent cogrinding followed by solution crystallization. In the binary cocrystals, uracil or 1-methyluracil with halide modification at the 5 position (F, Cl, Br, I) was coupled with amino-aromatic N-heterocycles (melamine, 2,4,6-triaminopyrimidine, 2,6-diaminopyridine) as a multivalent site for pyr…

proton transferPyrimidineX ray diffractionSupramolecular chemistry010402 general chemistry01 natural sciencesaromatic compounds; hydrogen bonds; ionization; proton transfer; X ray diffractionNucleobaselaw.inventionchemistry.chemical_compoundlawionizationsingle crystal X-raysGeneral Materials ScienceCrystallizationta116orgaaniset yhdisteet010405 organic chemistryHydrogen bondChemistryaromatic compoundsUracilGeneral ChemistrykiteetCondensed Matter Physics0104 chemical sciencesCrystallographyhalogen bondinghydrogen bondsTernary operationSingle crystalCrystal Growth & Design
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