Search results for "methane"

showing 10 items of 1763 documents

Vergleichende Untersuchung zur Diastereoselektivität derO-Methylierung von sterisch behinderten β-Ketocarbonsäureestern und ihren Enolen

1990

Diastereoselectivity of the O-Methylation of Sterically Hindered β-Ketocarboxylates and Their Enols The enols 1a, b, and 1c, which exists almost completely in the keto form, have been methylated at the oxygen atom with diazomethane. The regioselective reaction can be catalyzed by methanol, but may loose in that case the diastereoselectivity. A comparison with the methylation of the enolates by iodomethane is discussed.

chemistry.chemical_classificationSteric effectsDiazomethaneOrganic ChemistryRegioselectivityMethylationMedicinal chemistryCatalysischemistry.chemical_compoundOxygen atomchemistryEnol etherOrganic chemistryMethanolPhysical and Theoretical ChemistryLiebigs Annalen der Chemie
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Self-Assembly, Characterisation, and Crystal Structure of Multinuclear Metal Complexes of the [2×3] and [3×3] Grid-Type

2002

The self-assembly of new multimetallic complexes of grid-type architecture is described. The binding of a set of tris-terdentate ligands, 1 a-1 d, based on terpyridine-like subunits, with different octahedrally coordinated metal ions leads to the formation of species whose structure depends strongly on the ligand, the metal ion, the counterion, the solvent, and the reaction conditions. Under suitable conditions, the [3 x 3] grid was obtained from the reaction of ligand 1 a with zinc tetrafluoroborate and from ligand 1 b with mercury triflate. The other ligands led to the formation of mainly one compound of composition [M(6)L(5)](12+), which has the structure of an incomplete [2 x 3] grid. T…

chemistry.chemical_classificationSteric effectsStereochemistryLigandOrganic ChemistrySupramolecular chemistryGeneral ChemistryCrystal structureCatalysisNon-innocent ligandCoordination complexCrystallographychemistryCounterionTrifluoromethanesulfonateChemistry - A European Journal
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Synthesis of new polymers via Diels–Alder reaction. III. Biscyclohexadienephthalimides as dienes

1993

Difunctional cyclohexadienes with dihydrophthalimide central unitsand phenyl side groups to increase solubility are used as bisdienes in repetitive Diels-Alder polyadditions with bis(4-(1,2,4,-triazoline-3,5-dione-4-yl)phenyl)methane as a difunctional dienophile. The polymers show good solubility in CH 2 Cl 2 and CHCl 3 . Non-stoichiometric Diels-Alder polyaddition with slight excess of the bistriazolinedione provides the possibility of synthesizing telechelics with highly reactive triazolinedione end groups

chemistry.chemical_classificationTelechelic polymerMaterials sciencePolymers and PlasticsOrganic ChemistryCyclohexadienesPolymerMethanechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryOrganic chemistrySolubilityDiels–Alder reactionPolymer International
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Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts.

2004

Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)-imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions p…

chemistry.chemical_classificationTitaniumMolecular StructureChemistryGermaniumOrganic ChemistryThioanisoleInorganic chemistryGeneral ChemistrySulfidesHeterogeneous catalysisSilicon DioxidePeroxideCatalysisCatalysischemistry.chemical_compoundPyrimidinesCatalytic oxidationIonic liquidSolventsParticle SizeTrifluoromethanesulfonateOxidation-ReductionPorosityAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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Natural organic matter coagulation in Valencia water supply. Pilot plant studies

1998

: To reduce disinfection by-product (DBP) formation in drinking water treatment, the presence of natural organic matter in surface waters must be minimised. This paper describes pilot plant studies carried out on two surface waters to assess the effectiveness of coagulation in organic matter removal, the Turia and Jucar rivers, which supply the city of Valencia (1m inhabitants). The experiments were conducted with different coagulants (iron sulphate, polyaluminium chloride (PACl)) and treatment schemes. Process effectiveness was evaluated in terms of effluent turbidity, presence of residual metal in final water, and organic matter removal. Four parameters were used to quantify organic matte…

chemistry.chemical_classificationTotal organic carbonEnvironmental EngineeringChemistryHealth Toxicology and MutagenesisPermanganateTrihalomethanechemistry.chemical_compoundPilot plantEnvironmental chemistryOrganic matterWater treatmentTurbidityEffluentWater Science and TechnologyJournal of Water Supply: Research and Technology—AQUA
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Oxo and Hydroxo Tantalocene Complexes:  Synthesis and Reactivity. X-ray Molecular Structures of [(η5-Cp*)TaCl(OH)(η5-C5H4SiMe3)]+Cl-, (η5-Cp*)TaCl(O)…

2005

Exposure of a THF solution of tantalocene dichloride complexes (η 5 -Cp*)TaCl 2 (η 5 -C 5 H 4 -SiMe 3 ) (1) and (η 5 -Cp*)TaCl 2 (η 5 -C 5 H 5 ) (2) to the ambient atmosphere for 12 h leads to the formation of new tantalum(V) cationic hydroxo complexes [(η 5 -Cp*)TaCl(OH)(η 5 -C 5 H 4 SiMe 3 )] + -Cl- (3) and [(η 5 -Cp*)TaCl(OH)(η 5 -C 5 H 5 )]+Cl - (4). This oxidation reaction is more rapid under oxygen atmosphere since the hydroxo complexes are obtained in better yields within only 15 min. The hydroxo complexes are easily deprotonated by base to generate oxo complexes 5 and 6, which, in turn, react with trimethylsilyl triflate, giving the corresponding cationic silylated complexes 7 and 8…

chemistry.chemical_classificationTrimethylsilylBase (chemistry)StereochemistryOrganic ChemistryCationic polymerizationMedicinal chemistryRedoxInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryTACLReactivity (chemistry)Physical and Theoretical ChemistrycomputerTrifluoromethanesulfonatecomputer.programming_languageOrganometallics
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Screening pretreatment methods to enhance thermophilic anaerobic digestion of pulp and paper mill wastewater treatment secondary sludge

2013

Abstract The effect of hydrothermal (150 °C for 10 min and 70 °C for 40 min), enzymatic (Accelerase 1500, 0.07 g/g volatile solids (VS)), ultrasound (45 kHz for 30 min) and chemical pretreatments (HNO3 at pH 3 and NaOH at pH 12) alone or in combination on the chemical composition and methane yield of the pulp and paper mill secondary sludge was studied in batch assays at 55 °C. In total, 12 different pretreatment combinations were compared. Chemical analyses showed that all pretreatments except for HNO3 and ultrasound pretreatments improved the organic matter solubilization. Among the studied pretreatments, hydrothermal (150 °C, 10 min) pretreatment alone or in combination with enzymatic an…

chemistry.chemical_classificationWaste managementChemistrybusiness.industryGeneral Chemical EngineeringPulp (paper)ta1172Paper millGeneral Chemistryengineering.materialPulp and paper industryIndustrial and Manufacturing EngineeringMethaneHydrolysisAnaerobic digestionchemistry.chemical_compoundWastewaterengineeringEnvironmental ChemistryOrganic matterSewage treatmentbusinessta218Chemical Engineering Journal
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ChemInform Abstract: Concave π-Prismand Hydrocarbon [2.2.2]Cyclophanes and Their Crystalline Ag-Triflate Complexes.

2010

New small concave hydrocarbon cyclophanes were prepared via the well-known HD-2SO2-method. The cyclophanes obtained are isomers of the very well-known [2.2.2]p,p,p-cyclophane, C24H24, a π-prismand efficiently complexing Ag+-ion. X-ray crystal structure determinations showed the bis-sulfide 7 (1,10-dithia[3.3.2]m,p,p-cyclophane) to be helically chiral and that the conformation of the parent hydrocarbon cyclophane 13 ([2.2.2]m,p,p-cyclophane) does not change dramatically upon complexation with the Ag+-ion. The 16- and 17-membered [2.2.2]m,m,p- and [2.2.2]m,p,p-cyclophane (15 and 16) also act as π-prismands and form surprisingly similar crystalline 1:1 Ag-triflate complexes (π-prismates) as th…

chemistry.chemical_classificationchemistry.chemical_compoundCrystallographyHydrocarbonchemistryStructure analysisStereochemistryGeneral MedicineCrystal structureTrifluoromethanesulfonateCyclophaneChemInform
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I(py)2BF4, ein neues Reagens: allgemeine Methode für die 1,2-Iodfunktionalisierung von Olefinen

1985

chemistry.chemical_classificationchemistry.chemical_compoundHydrocarbonChemistryGeneral MedicineMethanolMedicinal chemistryChemical reactionDichloromethaneAngewandte Chemie
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Synthesis, optical, and thermal properties of glassy trityl group containing luminescent derivatives of 2-tert-butyl-6-methyl-4H-pyran-4-one

2012

In this work we present simple preparation of original trityl group containing glassy luminescent 6-styryl substituted derivatives of 2-(2-tert-butyl-4H-pyran-4-ylidene)malononitrile (DWK-1TB), 2-(2-tert-butyl-4H-pyran-4-ylidene)-2- ethyl-2-cyanoacetate (KWK-1TB), 2-(2-tert-butyl-4H-pyran-4-ylidene)-1H-indene-1,3(2H)-dione (ZWK-1TB) and 5-(2-tert-butyl-4H-pyran-4-ylidene)pyrimidine-2,4,6(1H,3H,5H)-trione (JWK-1TB). Their optical properties have been investigated. The absorption maxima of synthesized glasses is in region from 425 nm to 515 nm and emission maxima is from 470 nm to 625 nm in solution of dichloromethane. But absorption maxima of their solid films is from 425 nm to 500 nm and em…

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryThermal decompositionPhysical chemistryThermal stabilityPolymerAbsorption (chemistry)Glass transitionLuminescenceDichloromethaneMalononitrileOrganic Photonics V
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