Search results for "Chloromethane"

showing 10 items of 692 documents

CCDC 104283: Experimental Crystal Structure Determination

1997

Related Article: J.Ratilainen, K.Airola, M.Nieger, M.Bohme, J.Huuskonen, K.Rissanen|1997|Chem.-Eur.J.|3|749|doi:10.1002/chem.19970030515

Dicyclohexyl-11'-dispiro-715-(311-di(13)benzena-614-di(14)-26-dimethylbenzena-816-di(14)-35-dimethylbenzena-15913-tetraoxa-hexadecaphane) bis(dichloromethane) clathrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Thermal and optical properties of red luminescent glass forming symmetric and non symmetric styryl-4H-pyran-4-ylidene fragment containing derivatives

2012

Abstract Dyes with amorphous structure deposited from organic solvents and having good fluorescence properties show potential for photonic device applications. Organic glass-forming symmetric and non symmetric styryl- derivatives of 2(2,6-substituted-4H-pyran-4-ylidene)-malononitrile (it has backbone of known laser dye 4-(dicyanomethylene)-2-methyl-6-[p-(dimethylamino)styryl]-4H-pyran), 2(2,6-substituted-4H-pyran-4-ylidene)-1H-indene-1,3(2H)-dione and 2(2,6-substituted-4H-pyran-4-ylidene)-pyrimidine-2,4,6(1H,3H,5H)-trione were synthesized and investigated. Glass transition temperatures higher than 110 °C were achieved. The absorption bands in dichloromethane solution cover the spectral regi…

Dye laserPhotoluminescenceChemistryOrganic ChemistryPhotochemistryFluorescenceAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsAmorphous solidInorganic Chemistrychemistry.chemical_compoundPyranElectrical and Electronic EngineeringPhysical and Theoretical ChemistryGlass transitionLuminescenceSpectroscopyDichloromethaneOptical Materials
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Chlorinated short chain aliphatic hydrocarbons in pine needles by purge and trap gas chromatography/mass spectrometry

1995

The concentrations of volatile chlorinated short chain aliphatic hydrocarbons in pine needles have been measured using purge and trap GC/MS. The concentrations of dichloromethane, chloroform, dichloroethene and tetrachloroethene in the needles were calculated. The concentrations of dichloromethane and tetrachloroethene were highest. As a rule the concentrations were higher in the older needles. The needle samples were collected from five sampling points in an area situated in the Southern Finland in the vicinity of a metal scrab plant. Reference needles were collected in the Central Finland. Needles originated from years 1991, 1992 and 1993.

Environmental EngineeringChromatographyChloroformHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryDichloroethenePollutionPurge and trapchemistry.chemical_compoundchemistryEnvironmental chemistryEnvironmental ChemistryGas chromatography–mass spectrometryDichloromethaneChemosphere
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Interaction of half-sandwich alkylmolybdenum(III) complexes with B(C6F5)3. The X-ray structure of [CpMo(η4-C4H6)(μ-Cl)(μ-CH2)(O)MoCp][CH3B(C6F5)3]

2001

Abstract The reactions of the half-sandwich molybdenum(III) complexes CpMo(η 4 -C 4 H 4 R 2 )(CH 3 ) 2 , where Cpη 5 -C 5 H 5 and RH or CH 3 , with equimolar amounts of B(C 6 F 5 ) 3 have been investigated in toluene. EPR monitoring shows the formation of an addition product which does not readily react with Lewis bases such as ethylene, pyridine, or PMe 3 . The analysis of the EPR properties and the X-ray structure of a decomposition product obtained from dichloromethane, [CpMo(η 4 -C 4 H 6 )(μ-Cl)(μ-CH 2 )(O)MoCp][CH 3 B(C 6 F 5 ) 3 ], indicate that the borane attack has occurred at the methyl position.

EthyleneStereochemistrychemistry.chemical_elementBorane010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundlawPyridineMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryLewis acids and basesPhysical and Theoretical ChemistryElectron paramagnetic resonanceDichloromethaneMolybdenumEPR properties010405 organic chemistryOrganic ChemistryTolueneButadiene ligand0104 chemical sciences3. Good healthchemistryHalf-sandwichMolybdenumX-ray structure
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HPTLC and GC-MS for separation and identification of eugenol in plants

2007

Samples of clove, nutmeg, and cinnamon have been extracted by maceration with ethanol for 24 h and with aqueous ethanol 48 h. Rhizomes of herb bennet ( Geum urbanum ) and calamus ( Aconum calamus ) and roots of valerian ( Valeriana officinalis ) have been subjected to aqueous hydrolysis then extraction with dichloromethane. The active principles from the samples were separated on silica gel HPTLC plates, with pure (standard) and dental (pharmaceutical) eugenol, using n -heptane-ethyl acetate 60+40 ( v / v ) as mobile phase. After development the components were visualized in UV light at λ = 254 nm. The presence of eugenol was confirmed by GC-MS.

Geum urbanumValeriana officinalisChromatographybiologySilica gelClinical BiochemistryNutmegbiology.organism_classificationBiochemistryfood.foodAnalytical ChemistryEugenolchemistry.chemical_compoundfoodchemistryMaceration (wine)Gas chromatography–mass spectrometryDichloromethaneJournal of Planar Chromatography – Modern TLC
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Use of green alternative solvents in dispersive liquid‐liquid microextraction: A review

2021

Dispersive liquid-liquid microextraction is one of the most widely used microextraction techniques currently in the Analytical Chemistry field, mainly due to its simplicity and rapidity. The operational mode of this approach has been constantly changing since its introduction, adapting to new trends and applications. Most of these changes are related to the nature of the solvent employed for the microextraction. From the classical halogenated solvents (e.g., chloroform or dichloromethane), different alternatives have been proposed in order to obtain safer and non-pollutants microextraction applications. In this sense, low density solvents, such as alkanols, switchable hydrophobicity solvent…

Green chemistryMaterials scienceSupramolecular chemistryFiltration and SeparationAnalytical ChemistryDeep eutectic solventSolventchemistry.chemical_compoundchemistryChemical engineeringIonic liquidLow densityLiquid liquidDichloromethaneJournal of Separation Science
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The H2C(X)–X•••X– (X = Cl, Br) Halogen Bonding of Dihalomethanes

2017

The dihalomethane–halide H2C(X)–X···X– (X = Cl, Br) halogen bonding was detected in a series of the cis-[PdX(CNCy){C(NHCy)═NHC6H2Me2NH2}]X•CH2X2 (X = Cl, Br) associates by single-crystal XRD followed by DFT calculations. Although ESP calculations demonstrated that the σ-hole of dichloromethane is the smallest among all halomethane solvents (the maximum electrostatic potential is only 2.6 kcal/mol), the theoretical DFT calculations followed by Bader’s QTAIM analysis (M06/DZP-DKH level of theory) confirmed the H2C(X)–X···X– halogen bond in both the solid-state and gas-phase optimized geometries. The estimated bonding energy in H2C(X)–X···X– is in the 1.9–2.8 kcal/mol range.

Halogen bond010405 organic chemistryHalomethaneGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesdihalomethanes0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryComputational chemistryhalogen bondingGeneral Materials ScienceBond energyta116DichloromethaneCrystal Growth and Design
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trans-Bis[bis(diphenylphosphino)methane-κ2P,P′]dichlororuthenium(II) dichloromethane disolvate acetone hemisolvate hemihydrate

2006

Submitted by António Freitas (amsf@uma.pt) on 2019-06-14T10:31:02Z No. of bitstreams: 1 trans-Bis[bis(diphenylphosphino)methane-j2P,P000]dichlororuthenium(II) dichloromethane disolvate acetone hemisolvate hemihydrate.pdf: 221219 bytes, checksum: 8e4738b39248ecff6cd2421345c563e7 (MD5) Made available in DSpace on 2019-06-14T10:31:02Z (GMT). No. of bitstreams: 1 trans-Bis[bis(diphenylphosphino)methane-j2P,P000]dichlororuthenium(II) dichloromethane disolvate acetone hemisolvate hemihydrate.pdf: 221219 bytes, checksum: 8e4738b39248ecff6cd2421345c563e7 (MD5) Previous issue date: 2006 info:eu-repo/semantics/publishedVersion

Hemihydratechemistry.chemical_elementGeneral Chemistry.Condensed Matter PhysicsMedicinal chemistryMethaneRutheniumFaculdade de Ciências Exatas e da Engenhariachemistry.chemical_compoundchemistryAcetoneGeneral Materials Sciencetrans-Bis[bis(diphenylphosphino)methane-j2PP000]dichlororuthenium(II) dichloromethane disolvate acetone hemisolvate hemihydrateDichloromethaneActa Crystallographica Section E Structure Reports Online
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Porous zirconia and titania as packing materials for high-performance liquid chromatography

1990

Abstract Porous amorphous zirconia (ZrO 2 ) and titania (TiO 2 ) packings were synthesized as rigid microparticulate beads by means of a sol—gel process. Sufficient rigidity and desired mesoporosity of the ZrO 2 and TiO 2 particles were achieved only by a gel hardening process, followed by heat treatment. The mean pore diameter, p d , the specific surface area, a s , and the specific pore volume, ν p , were controlled by the heat treatment. Typical values were p d = 8 nm, a s = 80 m 2 /g and ν p = 0.23 ml/g. ZrO 2 - and TiO 2 -based revesed-phase packings were prepared by subjecting the native materials to a specific activation process and reaction with octadecyltrimethoxysilane. Native ZrO…

HeptaneChromatographyElutionOrganic ChemistryOctadecyltrimethoxysilaneGeneral MedicineBiochemistryAnalytical Chemistrylaw.inventionAmorphous solidchemistry.chemical_compoundchemistrylawSpecific surface areaCalcinationCubic zirconiaDichloromethaneJournal of Chromatography A
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Organocatalytic enantioselective aminoalkylation of pyrazol-3-ones with aldimines generated in situ from α-amido sulfones

2019

Herein, an efficient asymmetric aminoalkylation of pyrazolones with α-amido sulfones catalyzed by a quinine-derived squaramide in dichloromethane/aqueous media has been established. A variety of chiral amines were obtained with high yields (up to 98%) and excellent enantioselectivities (up to 99% ee). The corresponding products are transformed into optically active acetylated pyrazoles after treatment with Ac2O/Et3N, because of the instability of some adducts. The reaction tolerates a wide range of α-amido sulfones and different pyrazolones.

In situchemistry.chemical_classificationAldimine010405 organic chemistryOrganic ChemistryEnantioselective synthesisSquaramide010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesAdductCatalysischemistry.chemical_compoundCatàlisichemistryPyrazolonesOrganic chemistryPhysical and Theoretical ChemistryQuímica orgànicaDichloromethaneOrganic & Biomolecular Chemistry
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