Search results for "Fluorine Compounds"

showing 10 items of 13 documents

Diode laser spectroscopy of the nu(8) band of the SF(5)Cl molecule.

2003

Abstract Diode laser spectra of SF 5 Cl have been recorded in the ν 8 band region at a temperature of ca. 240 K, a pressure of 0.25 mbar and an instrumental bandwidth of ca. 0.001 cm −1 . Four regions have been studied: a first one in the P -branch (906.849–907.687 cm −1 ), a second one in the Q -branch (910.407–910.944 cm −1 ), and two other ones in the R -branch (913.957–914.556 and 917.853–918.705 cm −1 ). The whole ν 1 / ν 8 dyad of SF 5 35 Cl has been previously recorded in the group of Professor H. Burger in Wuppertal, thanks to a Fourier transform infrared spectrometer [J. Mol. Spectrosc. 208 (2001) 169]. These data have thus been combined with our diode laser ones in the aim of refi…

Sulfur CompoundsChemistryLasersFluorine CompoundsAnalytical chemistryInfrared spectroscopyLaserAtomic and Molecular Physics and OpticsSpectral lineAnalytical Chemistrylaw.inventionsymbols.namesakeFourier transformChlorideslawSpectrophotometryData Interpretation StatisticalsymbolsAtomic physicsFourier transform infrared spectroscopyGround stateHamiltonian (quantum mechanics)InstrumentationSpectroscopyDiodeSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Solution-, solid-phase, and fluorous synthesis of beta,beta-difluorinated cyclic quaternary alpha-amino acid derivatives: a comparative study.

2008

The diastereoselective synthesis of cyclic beta,beta-difluorinated alpha-amino acid derivatives bearing a quaternary stereocenter is described. The process relies on the chemo- and diastereoselective addition of allylic organometallic reagents to fluorinated alpha-imino esters and a subsequent ring-closing metathesis reaction (RCM). Complete selectivity in the nucleophilic addition was achieved with (R)-phenylglycinol methyl ether as a chiral auxiliary. The resulting amino acids were introduced into peptide chains, which could facilitate the preparation of potentially bioactive dipeptide derivatives. In addition, the solution synthesis of these cyclic fluorinated alpha-amino acids was succe…

Chiral auxiliaryAllylic rearrangementNucleophilic additionDipeptideMolecular StructureChemistryOrganic ChemistryFluorine CompoundsAmino Acids CyclicEtherEstersStereoisomerismGeneral ChemistryCatalysisStereocenterSolutionschemistry.chemical_compoundSolid-phase synthesisSalt metathesis reactionOrganic chemistryIminesProtonsAminationChemistry (Weinheim an der Bergstrasse, Germany)
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Effect of protonation and deprotonation on the gas phase reactivity of fluorinated 1,2,4-triazines

2008

Positive and negative electrospray mass spectrometry (MS), in-time and in-space MS n experiments, high-resolution and accurate mass measurements obtained with an Orbitrap, together with density functional theory calculations have been used to study the gas-phase ion chemistry of a series of fluorinated 1,2,4-triazines. As a result of low-energy collision-induced dissociations, occurring in an ion trap and in a triple quadrupole, their protonated and deprotonated molecules show interesting features depending on the nature and structure of the precursor ions. The occurrence of elimination/hydration reactions produced by positive ions in the ion trap is noteworthy. Decompositions of deprotonat…

Models MolecularSpectrometry Mass Electrospray IonizationIONIZATION MASS-SPECTROMETRYFluorine CompoundsAnalytical chemistryProtonationTandem mass spectrometryPhotochemistryOrbitrapIonlaw.inventionchemistry.chemical_compoundDeprotonationStructural BiologylawCHEMISTRYMoleculeComputer SimulationPhysics::Chemical PhysicsNEGATIVE ELECTROSPRAY-IONIZATIONCOLLISION-INDUCED DISSOCIATIONSpectroscopyTRIAZINESHYDRAZINEchemistryModels ChemicalHydroxyl radicalIon trapProtonsFRAGMENTATIONHETEROCYCLES
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Ab initio calculations of pure and Co+2-doped MgF2 crystals

2020

This research was partly supported by the Kazakhstan Science Project № AP05134367«Synthesis of nanocrystals in track templates of SiO2/Si for sensory, nano- and optoelectronic applications», as well as by Latvian Research Council project lzp-2018/1-0214. Calculations were performed on Super Cluster (LASC) in the Institute of Solid State Physics (ISSP) of the University of Latvia. Authors are indebted to S. Piskunov for stimulating discussions.

AB INITIO CALCULATIONSNuclear and High Energy PhysicsMaterials scienceSpin statesBand gapAb initioENERGY GAP02 engineering and technologyFLUORINE COMPOUNDS01 natural sciences7. Clean energyMolecular physicsAb initio quantum chemistry methodsCobalt dopant0103 physical sciencesPhysics::Atomic and Molecular Clusters:NATURAL SCIENCES:Physics [Research Subject Categories]MgF2010306 general physicsFluorideInstrumentationCOBALT DOPANTSDopantCRYSTAL ATOMIC STRUCTUREDopingCOBALT COMPOUNDSMAGNESIUM COMPOUNDSDOPANT ENERGY LEVELS021001 nanoscience & nanotechnologyVIBRATIONAL STRUCTURESCALCULATIONSCRYSTALSGROUND STATELinear combination of atomic orbitalsCELL PROLIFERATIONAb initioGROUND STATE LEVELS0210 nano-technologyGround state
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Copper-catalyzed regioselective synthesis of (E)-β-fluorovinyl sulfones

2019

Organofluorine compounds are finding increasing application in a variety of fields such as pharmaceutical, agrochemical, and material sciences. However, given the scarcity of fluorine-containing natural products, advancement in this area depends almost entirely on the development of new synthetic methodologies. In this article, we present the synthesis of a series of previously undescribed (E)-&beta

Vinyl CompoundsPharmaceutical Sciencealkynyl sulfonesChemical synthesisArticleCatalysisAnalytical ChemistrySulfonelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryorganofluorine chemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical Chemistrycopper catalysisMolecular StructureOrganic ChemistryRegioselectivityFluorineHydrogen fluorideOrganofluorine chemistryβ-fluorovinyl sulfonechemistryChemistry (miscellaneous)regioselectivityCopper catalyzedMolecular MedicineOrganofluorine compoundshydrogenationCopper
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Highly Fluorinated 2,2′-Biphenols and Related Compounds: Relationship between Substitution Pattern and Herbicidal Activity

2013

A broad range of halogenated 2,2'-biphenols was tested for applicability as crop protection agents. The activity of these compounds toward four typical pest plants was observed after application by spraying of diluted solutions. Despite their rather simple structure, it was found that the studied compounds reveal a surprisingly high herbicidal impact. To gain a better understanding of the structure-activity relationship, specific sites of the molecule were chemically modified and the core structures thus gradually changed. The influence of the substitution pattern on the herbicidal properties is discussed, and conclusions on the active site of the biphenol structure are drawn. It was observ…

HalogenationMolecular StructurebiologyHerbicidesChemistryFluorine CompoundsSubstitution (logic)Active siteGeneral ChemistryStructure-Activity Relationshipchemistry.chemical_compoundPhenolsHalogenbiology.proteinMoietyOrganic chemistryPhenolMoleculeGeneral Agricultural and Biological SciencesJournal of Agricultural and Food Chemistry
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Preparation and Promotion of Fruit Growth in Kiwifruit of Fluorinated N-Phenyl-N‘-1,2,3-thiadiazol-5-yl Ureas

2004

Seventeen phenyl-fluorinated analogues of thidiazuron [N-phenyl-N'-(1,2,3-thiadiazol-5-yl)urea, TDZ] have been prepared and characterized. The effects of each fluorinated urea on growth and quality of kiwifruits (Actinidia deliciosa) were evaluated by comparison with untreated (control) and TDZ-treated fruits. The results obtained showed a clear dependence of the growth-promoting activity of these fluorinated ureas on the pattern and degree of fluorine substitution in the phenyl ring. The most effective for promoting fruit growth was N-(2,3,5,6-tetrafluorophenyl)-N'-(1',2',3'-thiadiazol-5'-yl)urea at 25 ppm (at harvest, treated fruits were 58% heavier than untreated ones) followed by N-(3,5…

Actinidia deliciosaGrowth promotingbiologyChemistryPhenylurea CompoundsActinidiaFluorine CompoundsQuantitative Structure-Activity RelationshipTitratable acidGeneral Chemistrybiology.organism_classificationchemistry.chemical_compoundSoluble solidsFruitThidiazuronThiadiazolesBotanyUreaDry matterGeneral Agricultural and Biological SciencesNuclear chemistryJournal of Agricultural and Food Chemistry
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Improved Regioselectivity in Pyrazole Formation through the Use of Fluorinated Alcohols as Solvents: Synthesis and Biological Activity of Fluorinated…

2008

The preparation of N-methylpyrazoles is usually accomplished through reaction of a suitable 1,3-diketone with methylhydrazine in ethanol as the solvent. This strategy, however, leads to the formation of regioisomeric mixtures of N-methylpyrazoles, which sometimes are difficult to separate. We have determined that the use of fluorinated alcohols such as 2,2,2-trifluoroethanol (TFE) and 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as solvents dramatically increases the regioselectivity in the pyrazole formation, and we have used this modification in a straightforward synthesis of fluorinated analogs of Tebufenpyrad with acaricide activity. Fil: Fustero, Santos. Universidad de Valencia; España Fil…

MethylhydrazineFLUORINATED PYRAZOLFluorine CompoundsAlcoholPyrazoleMethylationChemical synthesisPYRAZOLchemistry.chemical_compoundAnimalsOrganic chemistryAcariDiketoneTebufenpyradMolecular StructureChemistryOrganic ChemistryCiencias QuímicasRegioselectivityStereoisomerismFLUOROUSPhenylhydrazinesSolventQuímica OrgánicaAlcoholsSolventsPyrazolesTEBUFENPYRADCIENCIAS NATURALES Y EXACTASThe Journal of Organic Chemistry
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Depth profiles of aggregate centers and nanodefects in LiF crystals irradiated with 34 MeV 84Kr, 56 MeV 40Ar and 12 MeV 12C ions

2018

I. Manika, J. Maniks and R. Zabels acknowledge the national project IMIS2. A. Dauletbekova, A. Akilbekov, M. Zdorovets and A. Seitbayev acknowledge the GF AP05134257of Ministry of Education and Science the Republic of Kazakhstan.

IONSMaterials sciencePhotoluminescenceF2 AND F3^+ CENTERSDislocationsAGGREGATESFLUORINE COMPOUNDS02 engineering and technologyETCHING7. Clean energy01 natural sciencesFluenceENERGY DISSIPATIONIonIRRADIATION EXPERIMENTSLIF CRYSTALION BOMBARDMENT0103 physical sciencesF2 and F3 + centersMaterials Chemistry:NATURAL SCIENCES:Physics [Research Subject Categories]IrradiationLUMINESCENCE INTENSITYPhotoluminescenceLITHIUM COMPOUNDS010302 applied physicsLiF crystalsNANOHARDNESSDISLOCATIONS (CRYSTALS)Surfaces and InterfacesGeneral ChemistryNanoindentation021001 nanoscience & nanotechnologyCondensed Matter PhysicsIsotropic etchingSurfaces Coatings and FilmsLASER SCANNING CONFOCAL MICROSCOPYNANOINDENTATION TECHNIQUESIon irradiationCOLOR CENTERSHardeningELECTRONIC ENERGY LOSSAtomic physicsDislocationLUMINESCENCE SIGNALS0210 nano-technologyLuminescenceDamage depth profiles
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The synthesis of fluorinated heteroaromatic compounds. Part 1. Five-membered rings with more than two heteroatoms. A review

2005

(2005). THE SYNTHESIS OF FLUORINATED HETEROAROMATIC COMPOUNDS. PART 1. FIVE-MEMBERED RINGS WITH MORE THAN TWO HETEROATOMS. A REVIEW. Organic Preparations and Procedures International: Vol. 37, No. 5, pp. 447-506.

13-DIPOLE ADDITION REACTIONSTETRASULFUR TETRANITRIDEChemistryOrganic ChemistryHeteroatomSUBSTITUTED 123-TRIAZOLES124-OXADIAZOLE SERIESSettore CHIM/06 - Chimica OrganicaORGANIC-CHEMISTRYEXPEDIENT ROUTEUNSATURATED NITROGEN-COMPOUNDSORGANOFLUORINE COMPOUNDSOrganic chemistryN-METHOXYTRIAZOLIUM SALTSHETEROCYCLIC-COMPOUNDS
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