Search results for "Halide"

showing 10 items of 324 documents

A Cation-Captured Palladium(0) Anion: Synthesis, Structure, and Bonding of [PdBr(PPh3)2]− Ligated by an N-Heterocyclic Phosphenium Cation

2009

Unsaturated N-heterocyclic phosphenium cations (uNHP) stabilize the [Pd0(PR3)2X]− anion proposed over the past decade to be the crucial but elusive intermediate in palladium-catalyzed cross-coupling reactions (X = halide). Insertion of metal into the P−Br bond of the precursor mesityl-substituted bromophosphine gives the structurally characterized Pd(0)-phosphenium complex (uNHPMes)Pd(PPh3)2Br, which features a long Pd−Br bond (2.7240(9) A) and the shortest known Pd−P bond (2.1166(17) A). The reaction is proposed to proceed by an associative pathway involving a Pd-bromophosphine complex that undergoes P-to-Pd bromide transfer.

ChemistryStereochemistryOrganic Chemistrychemistry.chemical_elementHalideIonInorganic ChemistryMetalchemistry.chemical_compoundBromidevisual_artPolymer chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryPalladiumOrganometallics
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Anionic halide···alcohol clusters in the solid state.

2014

The cationic (1,3,5-triazapentadiene)Pt(II) complexes [1](Cl)2, [2](Cl)2, [3](Br)2, and [4](Cl)2, were crystallized from ROH-containing systems (R = Me, Et) providing alcohol solvates studied by X-ray diffraction. In the crystal structures of [1-4][(Hal)2(ROH)2] (R = Me, Et), the Hal(-) ion interacts with two or three cations [1-4](2+) by means of two or three or four contacts thus uniting stacked arrays of complexes into the layers. The solvated MeOH or EtOH molecules occupy vacant space, giving contacts with [1-4](2+), and connects to the Hal(-) ion through a hydrogen bridge via the H(1O)O(1S) H atom forming, by means of the Hal(-)···HOR (Hal = Cl, Br) contact, the halide-alcohol cluster.…

ChemistryStereochemistrySolid-stateCationic polymerizationHalideAlcoholCrystal structureIonchemistry.chemical_compoundCrystallographyCluster (physics)MoleculePhysical and Theoretical Chemistryta116The journal of physical chemistry. A
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Hydrogen bond-stabilised N-alkylammonium resorcinarene halide cavitands

2010

A family of hydrogen bond-stabilised N-alkylammonium resorcinarene chloride and bromide cavitands were synthesised and characterised with 1H NMR and ESI mass spectrometry. The seven compounds exhibit interestingly either self-inclusion or guest complexation in the solid state evidenced by single crystal X-ray diffraction. The four dimers show self-inclusion of the upper rim propyl chains and consist of two hydrogen-bonded resorcinarene tetracations and six halide anions, while the remaining two halide anions are located in between the dimers linking them via hydrogen bonding. Small solvent molecules such as dichloromethane, methanol, n-butanol or chloroform are complexed into the resorcinar…

ChloroformHydrogen bondHalideGeneral ChemistryResorcinarenePhotochemistrySolventchemistry.chemical_compoundchemistryBromidePolymer chemistryProton NMRMoleculeresorcinarenes; tetrabenzoxazines; ammonium halides; hydrogen bonding; X-ray structure
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Gas phase chromatography of halides of elements 104 and 105

1992

On-line isothermal gas phase chromatography was used to study halides of261104 (T1/2=65 s) and262,263105 (T1/2=34 s and 27 s) produced an atom-at-a time via the reactions248Cm(18O, 5n) and249Bk(18O, 5n, 4n), respectively. Using HBr and HCl gas as halogenating agents, we were able to produce volatile bromides and chlorides of the above mentioned elements and study their behavior compared to their lighter homologs in Groups 4 or 5 of the periodic table. Element 104 formed more volatile bromide than its homolog Hf. In contrast, element 105 bromides were found to be less volatile than the bromides of the group 5 elements Nb and Ta. Both 104 and Hf chlorides were observed to be more volatile tha…

ChromatographyChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthHalideHydrochloric acidPollutionChemical reactionChlorideIsothermal processAnalytical Chemistrychemistry.chemical_compoundNuclear Energy and EngineeringBromidemedicineHydrobromic acidRadiology Nuclear Medicine and imagingGas chromatographySpectroscopymedicine.drugJournal of Radioanalytical and Nuclear Chemistry Articles
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New Austalides from the Sponge-Associated Fungus Aspergillus sp.

2011

Chromatographic separation of a crude extract obtained from the fungus Aspergillus sp., isolated from the Mediterranean sponge Tethya aurantium, yielded five new meroterpenoid metabolites, austalides M–Q (1–5), together with nine known compounds (6–13). The structures of the new compounds were unambiguously elucidated on the basis of extensive 1D and 2D NMR methods and by mass spectral analysis. Furthermore, the absolute configurations of 1 and 4 were determined by time-dependent density functional theory electronic circular dichroism (TDDFT ECD) calculations, allowing the assignment of the absolute configuration of analogous compounds 2, 3, and 5. The calculations revealed that the conform…

Circular dichroismbiologyStereochemistryChemistryOrganic ChemistryAbsolute configurationTime-dependent density functional theoryChromophorebiology.organism_classificationPhthalidechemistry.chemical_compoundTermészettudományokPhysical and Theoretical ChemistryTethya aurantiumKémiai tudományokCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopyEuropean Journal of Organic Chemistry
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Ruddlesden-Popper Hybrid Lead Bromide Perovskite Nanosheets of Phase Pure n=2: Stabilized Colloids Stored in the Solid State.

2021

Ruddlesden-Popper lead halide perovskite (RP-LHP) nano-nanostructures can be regarded as self-assembled quantum wells or superlattices of 3D perovskites with an intrinsic quantum well thickness of a single or a few (n=2-4) lead halide layers; the quantum wells are separated by organic layers. They can be scaled down to a single quantum well dimension. Here, the preparation of highly (photo)chemical and colloidal stable hybrid LHP nanosheets (NSs) of ca. 7.4 μm lateral size and 2.5 nm quantum well height (thereby presenting a deep blue emission at ca. 440 nm), is reported for the first time. The NSs are close-lying and they even interconnect when deposited on a substrate. Their synthesis is …

Col·loidesNanoestructuresPhotoluminescenceMaterials scienceSuperlatticeHalideGeneral Medicine02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesColloidChemical engineeringPhase (matter)Nanodot0210 nano-technologyQuantum wellPerovskite (structure)Angewandte Chemie (International ed. in English)
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Formation of self-trapped excitons through stimulated recombination of radiation-induced primary defects in alkali halides

1998

Abstract A self-trapped exciton formation through photostimulated recombination of an F and an H center — the exciton-created primary defect pair, is proposed and experimentally examined in alkali halides at low temperatures.

Condensed Matter::Quantum GasesPrimary (chemistry)PhotoluminescenceChemistryPhotostimulated luminescenceExcitonInorganic chemistryBiophysicsHalideRadiation inducedGeneral ChemistryCondensed Matter PhysicsAlkali metalPhotochemistryBiochemistryAtomic and Molecular Physics and OpticsCondensed Matter::Materials SciencePhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsPhysics::Chemical PhysicsRecombinationJournal of Luminescence
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Relativistic DFT Calculation of (119)Sn Chemical Shifts and Coupling Constants in Tin Compounds.

2006

The nuclear shielding and spin-spin coupling constants of (119)Sn in stannane, tetramethylstannane, methyltin halides Me4-nSnXn (X = Cl, Br, I; n = 1-3), tin halides, and some stannyl cations have been investigated computationally by DFT methods and Slater all-electron basis sets, including relativistic effects by means of the zeroth order regular approximation (ZORA) method up to spin-orbit coupling. Calculated (119)Sn chemical shifts generally correlate well with experimental values, except when several heavy halogen atoms, especially iodine, are bound to tin. In such cases, calculated chemical shifts are almost constant at the scalar (spin-free) ZORA level; only at the spin-orbit level i…

Coupling constantchemistry.chemical_classificationNMR spectroscopy; computational chemistry; tin compounds; tin-119Chemical shifttin compoundsHalidechemistry.chemical_elementOrganotin(IV) NMR DFT coupling constantstin-119Stannanecomputational chemistryComputer Science Applicationschemistry.chemical_compoundNMR spectroscopychemistryComputational chemistryHalogenPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryTinRelativistic quantum chemistryAlkylJournal of chemical theory and computation
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X‐irradiation induced photo‐ and thermostimulated luminescence of CsCdF 3 :Mn crystals

2005

Photo- and thermostimulated luminescence (PSL and TSL respectively) of previously X-irradiated CsCdF3 crystal doped with Mn were investigated. After X-irradiation of CsCdF3 crystal at 8 K PSL bands at about 300 nm and 550 nm appear. Several stimulation bands can be revealed for luminescence at 300 nm and 550 nm. The stimulation band at 340 nm is related to an F-type centre absorption band in accordance with the Mollwo-Ivey relation for halide crystals. Subsequent heating of the crystal after X-irradiation at 8 K shows TSL peaks in the temperature regions 8 K – 90 K and 200 K – 300 K. The spectral composition of the TSL involves both bands at 300 nm and 550 nm. Experiments performed allow us…

CrystalAbsorption bandChemistryDopingAnalytical chemistryHalideThermal stabilityIrradiationLuminescenceIonphysica status solidi (c)
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<title>High-excitation-density luminescence as probe of mixed silver halides</title>

1992

Two kinds of intrinsic luminescence in mixed AgBr1-xClx (1 io. Dependence of the parameters of this process on crystal composition has been investigated in terms of spatially well correlated Frenkel defect recombinations. The main effect found was the linear increase of the Agio migration energy with the crystal composition x. The second kind of luminescence arising due to exciton molecules has been shown to be sensitive to the solid solution composition and the quality of a crystal. It is shown that this luminescence correlates with the optical losses of the fibers studied.

CrystalMaterials scienceExcitonFrenkel defectMoleculeHalideLuminescenceMolecular physicsExcitationSolid solutionInfrared Fiber Optics III
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