Search results for "Chloromethane"

showing 10 items of 692 documents

Preparation and Structure of Bicycloalkane-Condensed Aryldiaziridines Accompanied by Pyrimidines

2007

Di-exo- and di-endo-2-aminonorbomane/enemethanamines 1-3, di-exo-oxanorbomene derivative 4 and cis-cyclohexane and trans-4-cyclohexene analogues 5, 6 were reacted with p-chlorobenzaldehyde in the presence of N-bromosuccinimide in dichloromethane. Via the reactions of 1-6, condensed diaziridines 7-12 accompanied by pyrimidine derivatives 13-16 were prepared after isolation with column chromatography. The mechanisms proposed for alternative transformations were supported by DFT calculations. The structures of the new compounds were proved by IR and NMR spectroscopy and, for 7, 9 and 12, also by means of X-ray crystallography.

Pharmacologychemistry.chemical_compoundColumn chromatographyDiaziridinechemistryPyrimidineComputational chemistryOrganic ChemistryOrganic chemistryGeneral MedicineNuclear magnetic resonance spectroscopyAnalytical ChemistryDichloromethaneHETEROCYCLES
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Efficient orange light-emitting electrochemical cells

2012

We report the first bis-cyclometalated cationic iridium(III) complex with N-aryl-substituted 1H-imidazo [4,5-f][1,10]phenanthroline. The complex emits yellow-orange phosphorescence with a maximum at 583 nm, a quantum yield of 43%, and an excited-state lifetime of 910 ns in argon-saturated dichloromethane. Optimized orange light-emitting electrochemical cells with the new Ir(III) complex exhibit fast turn-on, a peak luminance of 684 cd m(-2) and a peak efficacy of 6.5 cd A(-1); in 850 h of continuous operation their luminance and efficacy decrease only by 20%.

PhenanthrolineCationic polymerizationchemistry.chemical_elementQuantum yieldGeneral ChemistryOrange (colour)PhotochemistryElectrochemical cellchemistry.chemical_compoundchemistryMaterials ChemistryIridiumPhosphorescenceDichloromethaneJournal of Materials Chemistry
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New measurements and global analysis of chloromethane in the region from 0 to 1800cm−1

2003

Abstract New high resolution Fourier transform spectra of pure 12CH335Cl and 12CH337Cl isotopomers of chloromethane have been recorded in Wuppertal covering the region from 600 to 3800 cm−1. New rotational transitions within the v2=1, v5=1, and v3=2 states have been measured at Lille. A first global analysis of the lower four band systems of the molecule (700–1800 cm−1) is reported. The model was based on an effective Hamiltonian and dipole moment expressed in terms of irreducible tensor operators. A common set of 125 effective hamiltonian parameters (sixth order) has been adjusted to fit simultaneously some 11 000 IR data for each of the isotopomers including 153 mm wave data for 12 CH3 35…

PhysicsChloromethaneFourier transform spectraAtomic and Molecular Physics and OpticsHot bandStandard deviationIsotopomerssymbols.namesakeDipolechemistry.chemical_compoundNuclear magnetic resonancechemistrysymbolsMoleculePhysical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)SpectroscopyJournal of Molecular Spectroscopy
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New ground state constants of 12CH335Cl and 12CH337Cl from global polyad analysis

2005

Abstract A global analysis of the infrared spectrum of chloromethane involving the ground state and the 13 vibrational states lying up to 2600 cm −1 was recently achieved using high resolution Fourier transform spectra of pure isotopomers. More than 20 000 transitions (cold and hot bands) for each isotopomer 12 CH 3 35 Cl and 12 CH 3 37 Cl have been assigned and fitted with a standard deviation of about 3 × 10 −4  cm −1 close to the experimental precison. As part of this global effort, improved ground state constants up to sextic centrifugal distortion terms have been determined for each isotopomer taking advantage of the numerous allowed and perturtation-allowed transitions simultaneously …

PhysicsInfraredChloromethaneRotational–vibrational spectroscopyPolyadAtomic and Molecular Physics and OpticsStandard deviationIsotopomerschemistry.chemical_compoundNuclear magnetic resonancechemistryDistortionPhysical and Theoretical ChemistryAtomic physicsGround stateSpectroscopyJournal of Molecular Spectroscopy
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Experimental and theoretical DFT study of the reaction of 3-amino-1,2-diols with dichloromethane and paraformaldehyde

2004

Abstract The reactions of 3-phenyl-3-methylamino-1,2-propanediol 1a and 3-[(tert-butyldimethylsilyl)oxy]-1-methylamino-1-phenyl-2-propanol 1b with (CH2O)n and CH2Cl2 are appropriate procedures for the preparation of 1,3-oxazines or 1,3-oxazolidines under proper selection of kinetic or thermodynamic reaction conditions. The reaction of 1b with (CH2O)n or CH2Cl2, affords the oxazolidine 2b under kinetic conditions and then this compound can be slowly converted into 5-[(tert-butyldimethylsilyl)oxy]-3-methyl-4-phenyl-3,4,5,6-tetrahydro-2H-1,3-oxazine 3b under thermodynamic control. The mechanism proposed for this transformation and the effect of polar solvents on the acceleration of the reactio…

Reaction conditionschemistry.chemical_compoundOxazolidinechemistryComputational chemistryOrganic ChemistryDrug DiscoveryOrganic chemistryParaformaldehydeKinetic energyBiochemistryDichloromethaneTetrahedron
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CCDC 291811: Experimental Crystal Structure Determination

2006

Related Article: F.A.Cotton, C.A.Murillo, S.-E.Stiriba, Xiaoping Wang, Rongmin Yu|2005|Inorg.Chem.|44|8223|doi:10.1021/ic051282c

SSS-tris(mu4-benzene-14-dicarboxylato)-hexakis(mu2-2-(diphenylphosphino)phenyl)-hexapyridyl-hexa-rhodium dichloromethane methanol sesquihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 291816: Experimental Crystal Structure Determination

2006

Related Article: F.A.Cotton, C.A.Murillo, S.-E.Stiriba, Xiaoping Wang, Rongmin Yu|2005|Inorg.Chem.|44|8223|doi:10.1021/ic051282c

SSS-tris(mu~4~-benzene-14-dicarboxylato)-hexakis(mu~2~-2-(diphenylphosphino)phenyl)-tris(methanol)-tripyridyl-hexa-rhodium dichloromethane methanol solvate hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Thin-layer chromatography of chlorinated cresols

1977

Abstract The thin-layer chromatography of four chlorinated cresols was studied on five layer materials using eleven solvent systems. Sharp spots were obtained except on Kieselguhr G layers. The best separation of the individual compounds occurred on silica gel-containing layers with dichloromethane as the solvent. Each solvent system was found to cause a different separation on different layers.

SolventSolvent systemchemistry.chemical_compoundChromatographyChemistryOrganic ChemistryGeneral MedicineBiochemistryLayer (electronics)Thin-layer chromatographyAnalytical ChemistryDichloromethaneJournal of Chromatography A
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Silica-supported HgSO4/H2SO4: a convenient reagent for the hydration of alkynes under mild conditions

2010

Abstract The silica-supported aqueous-phase catalyst (SAPC) approach has proven convenient for efficiently performing the hydration of alkynes with HgSO 4 /H 2 SO 4 to give the corresponding carbonyl compounds in dichloromethane under mild conditions. The use of this solid reagent significantly improves the reaction work-up as it merely involves filtering and evaporating the solvent.

Solventchemistry.chemical_compoundchemistryReagentOrganic ChemistryDrug DiscoveryInorganic chemistryOrganic chemistrychemistry.chemical_elementBiochemistryDichloromethaneCatalysisMercury (element)Tetrahedron Letters
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CCDC 764359: Experimental Crystal Structure Determination

2010

Related Article: T.Voss, Chao Chen, G.Kehr, E.Nauha, G.Erker, D.W.Stephan|2010|Chem.-Eur.J.|16|3005|doi:10.1002/chem.200903483

Space GroupCrystallography((11-Dimethyl-23-dihydro-1H-indolium-2-yl)methyl)(tris(pentafluorophenyl))borate dichloromethane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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