Search results for "LF"

showing 10 items of 12543 documents

Spontaneous order in ensembles of rotating magnetic droplets

2019

Ensembles of elongated magnetic droplets in a rotating field are studied experimentally. In a given range of field strength and frequency the droplets form rotating structures with a triangular order - rotating crystals. A model is developed to describe ensembles of several droplets, taking into account the hydrodynamic interactions between the rotating droplets in the presence of a solid wall below the rotating ensemble. A good agreement with the experimentally observed periodic dynamics for an ensemble of four droplets is obtained. During the rotation, the tips of the elongated magnetic droplets approach close to one another. An expression is derived that gives the magnetic interaction be…

010302 applied physicsRange (particle radiation)Materials scienceField (physics)Dynamics (mechanics)Fluid Dynamics (physics.flu-dyn)FOS: Physical sciencesField strengthPhysics - Fluid Dynamics02 engineering and technologyCondensed Matter - Soft Condensed MatterSolid wall021001 nanoscience & nanotechnologyCondensed Matter PhysicsRotation01 natural sciencesMolecular physicsElectronic Optical and Magnetic MaterialsPhysics::Fluid DynamicsColloid0103 physical sciencesPhysics::Atomic and Molecular ClustersSoft Condensed Matter (cond-mat.soft)Self-assembly0210 nano-technology
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Multi-scale multireference configuration interaction calculations for large systems using localized orbitals: Partition in zones

2012

A new multireference configuration interaction method using localised orbitals is proposed, in which a molecular system is divided into regions of unequal importance. The advantage of dealing with local orbitals, i.e., the possibility to neglect long range interaction is enhanced. Indeed, while in the zone of the molecule where the important phenomena occur, the interaction cut off may be as small as necessary to get relevant results, in the most part of the system it can be taken rather large, so that results of good quality may be obtained at a lower cost. The method is tested on several systems. In one of them, the definition of the various regions is not based on topological considerati…

010304 chemical physicsChemistryGeneral Physics and AstronomyMultireference configuration interactionMolecular orbital theory010402 general chemistry01 natural sciences0104 chemical sciencesLinear combination of atomic orbitalsMulti-configurational self-consistent field0103 physical sciencesMolecular orbitalComplete active spaceStatistical physicsPhysical and Theoretical ChemistryAtomic physicsBasis setNatural bond orbital
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Matrix isolation and quantum chemical studies on the H2O2–SO2complex

2004

Complexation and photochemical reactions of hydrogen peroxide and sulfur dioxide have been studied in solid Ar, Kr and Xe. Complexes between H2O2 and SO2 are characterized using Fourier transform infrared spectroscopy and ab initio calculations. In solid Ar, the H2O2–SO2 complex absorptions are found at wavenumbers of 3572.8, 3518.7, 3511.2, 3504.3, 1340.3, 1280.2 and 1149.9 cm−1. In Kr and Xe matrices, the bonded OH stretching frequencies deviate from the values in Ar, and we propose that the matrix surrounding influences the structure of the H2O2–SO2 complex. UV photolysis of the H2O2–SO2 was also studied in solid Ar, Kr and Xe. This photolysis produces mainly a complex between sulfur tri…

010304 chemical physicsPhotodissociationMatrix isolationGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciences0104 chemical scienceschemistry.chemical_compoundMatrix (mathematics)chemistryComputational chemistryAb initio quantum chemistry methods0103 physical sciencesSulfur trioxidePhysical chemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyHydrogen peroxideSulfur dioxidePhys. Chem. Chem. Phys.
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A new hydrogen bonding motif involved in self-recognition in the solid state by functionalised macrocycles

2011

Self-recognition within the crystal lattices of three functionalised macrocycles results in the formation of arrays of remarkably similar hermaphroditic pairs of macrocycles. In the case of two of the macrocycles containing acylhydrazine substituents, a hitherto unknown recognition pattern is found in the interaction of the hydrazine moiety with crown-ether oxygen atoms.

010405 organic chemistryChemistryHydrogen bondStereochemistryHydrazineAcylhydrazineSolid-stateGeneral ChemistrySelf recognitionCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences3. Good health0104 chemical scienceschemistry.chemical_compoundOxygen atomPolymer chemistryMoiety[CHIM]Chemical SciencesGeneral Materials Scienceta116ComputingMilieux_MISCELLANEOUS
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Synthesis, reactivity and structural studies of carboranyl thioethers and disulfides.

2005

The equimolar reaction of 1-SH-2-R-1,2-closo-C2B10H10 (R = Me, H, Ph) with KOH in ethanol produces the thiolate species [1-S-2-R-1,2-closo-C2B10H10]−. These react with iodine to give the disulfide bridged dicluster (1-S-2-R-1,2-closo-C2B10H10)2 (R = H, Me, Ph) compounds as analytically pure, white and air-stable solids in high yield. Synthesis of monothioether bridged species is synthetically more difficult. In fact three procedures have been tested to obtain the thioether bridged dicluster compounds (2-R-1,2-closo-C2B10H10)2S (R = Me, H, Ph) but only (2-Me-1,2-closo-C2B10H10)2S was successfully synthesized and characterized. Attempts to produce mixed compounds (1-R-1,2-closo-C2B10H10)S(1-R…

010405 organic chemistryChemistryInorganic chemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesMedicinal chemistrySulfur0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundThioetherYield (chemistry)Cluster (physics)Reactivity (chemistry)CarbonHOMO/LUMODalton transactions (Cambridge, England : 2003)
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Advances in photochemical and electrochemical incorporation of sulfur dioxide for the synthesis of value-added compounds.

2021

Organic photochemistry and electrochemistry currently receive tremendous attention in organic synthesis as both techniques enable the reagent-less activation of organic molecules without using expensive and hazardous redox reagents. The incorporation of SO2 into organic molecules is a relatively modern research topic, which likewise gains immense popularity since the discovery of the SO2 surrogate DABSO. Sulfur-containing organic molecules are omnipresent in pharmaceuticals and agrochemicals. This review covers the recent progress in electrochemical and photochemical methodologies for the incorporation and uses of SO2 in the synthesis of value-added compounds. Additionally, different work t…

010405 organic chemistryChemistryMechanistic organic photochemistryMetals and AlloysGeneral Chemistry010402 general chemistryPhotochemistryElectrochemistrycomplex mixtures01 natural sciencesRedoxCatalysisrespiratory tract diseases0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOrganic moleculeschemistry.chemical_compoundMaterials ChemistryCeramics and CompositesOrganic synthesisSulfur dioxideChemical communications (Cambridge, England)
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Self-assembly of M4L4tetrahedral cages incorporating pendant PS and PSe functionalised ligands

2019

Herein, the synthesis of metal–organic tetrahedral cages featuring flexible thio- and selenophosphate-based ligands is described. The cages were prepared by sub-component self-assembly of AP(OC6H4NH2-4)3 (A = S, Se) or SP(SC6H4NH2-4)3, 2-pyridinecarboxaldehyde, and either Fe[BF4]2 or Co[BF4]2. Preliminary host–guest studies into the ability of the pendant PS and PSe groups to interact with suitable substrates will be discussed.

010405 organic chemistryChemistryMetals and AlloysThio-General Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPolymer chemistryMaterials ChemistryCeramics and CompositesTetrahedronSelf-assemblyChemical Communications
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Recent progress in the application of fluorinated chiral sulfinimine reagents

2018

Abstract The development of synthetic methodology allowing for a strategic incorporation of fluorine into target compounds is in a high demand in many areas of the chemical and pharmaceutical industries. In this regard, application of fluorinated chiral sulfinimine reagents, in particularly, N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimine, is one of the most general and practical approaches for preparation of compounds containing pharmacophoric fluoro-amino-keto/hydroxy moieties. This article provides a timely and comprehensive overview of the recent synthetic applications of fluorinated chiral sulfinimine reagents for asymmetric synthesis of fluoro-containing polyfunctional amino-compound…

010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisAsymmetric synthesisFluoro-imineAmino compounds010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesInorganic ChemistrySulfinimineReagentEnvironmental ChemistryPhysical and Theoretical ChemistryAmino compounds; Asymmetric synthesis; Fluoro-imine; Sulfinimine; Biochemistry; Environmental Chemistry; Physical and Theoretical Chemistry; Organic Chemistry; Inorganic ChemistryJournal of Fluorine Chemistry
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Late-Stage Modification of Electronic Properties of Antiaromatic and Diradicaloid Indeno[1,2-b]fluorene Analogues via Sulfur Oxidation

2020

The ability to alter optoelectronic and magnetic properties of molecules at a late stage in their preparation is in general a nontrivial feat. Here, we report the late-stage oxidation of benzothiop...

010405 organic chemistryChemistryOrganic ChemistryLate stagechemistry.chemical_elementFluoreneequipment and supplies010402 general chemistryPhotochemistry01 natural sciencesSulfur0104 chemical scienceschemistry.chemical_compoundMoleculehuman activitiesAntiaromaticityElectronic propertiesThe Journal of Organic Chemistry
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Oxoanion binding to a cyclic pseudopeptide containing 1,4-disubstituted 1,2,3-triazole moieties

2016

A macrocyclic pseudopeptide 3 is described featuring three amide groups and three 1,4-disubstituted 1,2,3-triazole units along the ring. This pseudopeptide was designed such that the amide NH groups and the triazole CH groups converge toward the cavity, thus creating an environment well suited for anion recognition. Conformational studies in solution combined with X-ray crystallography confirmed this preorganisation. Solubility of 3 restricted binding studies to organic media such as 5 vol% DMSO/acetone or DMSO/water mixtures with a water content up to 5 vol%. These binding studies demonstrated that 3 binds to a variety of inorganic anions in DMSO/acetone including chloride, nitrate, sulfat…

010405 organic chemistryChemistryStereochemistryDimerOrganic ChemistryTriazoleoxoanion bindings010402 general chemistry01 natural sciencesBiochemistryChlorideMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundpseudopeptidesStability constants of complexesAmidemedicineMoleculePhysical and Theoretical ChemistrySulfateSolubilityta116medicine.drugOrganic & Biomolecular Chemistry
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