Search results for "Amine gas treating"

showing 10 items of 252 documents

Formation of novel T-shaped NNN ligands via rare-earth metal-mediated Si-H activation.

2014

Reactions of silylamides [Ln{N(SiHMe2)2}3(thf)2] with sterically crowded terphenylamine DmpNH2 (Dmp = 2,6-Mes2C6H3 with Mes = 2,4,6-Me3C6H2) afforded via a template reaction the formation of a new tridentate ligand, and derived complexes of composition [LnN{SiMe2N(Dmp)}2] (Ln = Ce, Pr) were obtained. Usage of the even more bulky amine Ar*NH2 (Ar* = 2,6-Trip2C6H3 with Trip = 2,4,6-iPr3C6H2) yielded the free protonated ligand NH{SiMe2NH(Ar*)}2.

Steric effectsTridentate ligandChemistryLigandStereochemistryRare earthProtonationInorganic ChemistryMetalTemplate reactionCrystallographyvisual_artvisual_art.visual_art_mediumAmine gas treatingPhysical and Theoretical ChemistryInorganic chemistry
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PHOSPHORORGANISCHE VERBINDUNGEN 991VERSUCHE ZUR AUFKLÄRUNG DER O-SELEKTIVITÄT VON VERBINDUNGEN MIT DER P(O)F-GRUPPE

1982

Abstract The mechanism of the reaction of phosphoryl fluoride ( P(O)F) with alcohols in the presence of an amine is fundamentally different from the reaction of phosphoryl chlorides ( P(O)Cl) with primary or secondary amines. The following observations strongly support this proposal: 1. 1H-NMR-, 31P-NMR- and 19F-NMR-spectroscopic investigations show that methyl-phenyl-phosphinicacid-fluoride and n-butylamine form a thermolabile adduct, which yields the methyl-phenyl-phosphinicacid-amide only very slowly. 2. The rate of the reaction of methyl-phenyl-phosphinicacid-fluoride with ethanol is independent of the basicity of the amine but very sensitive to steric factors. Imidazole (which is only …

Steric effectschemistry.chemical_compoundPhosphoryl fluoridechemistryStereochemistryImidazoleAmine gas treatingMethanolThermolabileWeak baseMedicinal chemistryAdductPhosphorus and Sulfur and the Related Elements
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Substituent effects in trans-p,p'-disubstituted azobenzenes: X-ray structures at 100 K and DFT-calculated structures.

2014

The crystal and molecular structures of twopara-substituted azobenzenes with π-electron-donating –NEt2and π-electron-withdrawing –COOEt groups are reported, along with the effects of the substituents on the aromaticity of the benzene ring. The deformation of the aromatic ring around the –NEt2group inN,N,N′,N′-tetraethyl-4,4′-(diazenediyl)dianiline, C20H28N4, (I), may be caused by steric hindrance and the π-electron-donating effects of the amine group. In this structure, one of the amine N atoms demonstrates clearsp2-hybridization and the other is slightly shifted from the plane of the surrounding atoms. The molecule of the second azobenzene, diethyl 4,4′-(diazenediyl)dibenzoate, C18H18N2O4,…

Steric effectscrystal structureChemistryStereochemistry4electron-donating effectsSubstituentAromaticityCrystal structureDFT calculationsCondensed Matter PhysicsInorganic ChemistryCrystalelectron-withdrawing effectsHOMA indexCrystallographychemistry.chemical_compoundMaterials Chemistry4'-(diazenediyl)dibenzoateAmine gas treatingDensity functional theoryPhysical and Theoretical Chemistryazo­benzenesBenzene4'-(diazene­diyl)dianilineActa crystallographica. Section C, Structural chemistry
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Ligand substitution reactions of the [ReX6]2− (X=Cl, Br) anions. Synthesis and crystal structure of novel oxalato complexes of rhenium(IV)

2006

Abstract The reaction of K2[ReX6] (X = Cl, Br) with oxalic acid and triethylamine in dimethylformamide solution yields the substituted complexes [ReX4(ox)]2− and cis-[ReX2(ox)2]2−, which can be obtained separately depending on the amount of added amine. The crystal structures of (PPh4)2[ReBr4(ox)], cis-(PPh4)2[ReBr2(ox)2] and cis-(AsPh4)2[ReCl2(ox)2] have been determined by single-crystal X-ray diffraction. The anionic complexes are octahedral with only slight distortions. The direct isolation of the pure complexes as well as the formation of only the cis isomers – without the presence of trans isomers and/or [Re(ox)3]2− – is probably due to the kinetic inertness of Re(IV)–X bonds, which in…

Substitution reactionChemistryStereochemistryLigandchemistry.chemical_elementCrystal structureRheniumMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryDimethylformamideAmine gas treatingPhysical and Theoretical ChemistryTriethylamineCis–trans isomerismInorganica Chimica Acta
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Polyaza[n](1,4)naphthalenophanes and polyaza[n](9,10)anthracenophanes

2002

Abstract A series of polyaza[n](1,4)naphthalenophanes and polyaza[n](9,10)anthracenophanes have been prepared by using the Fukuyama's protecting group (2- or 4-nitrophenyl sulfonyl) in a one-pot cyclization–deprotection reaction. Global yields for the purified products are comparable with those obtained for other polyazacyclophanes using the tosyl group as the amine protecting group. Their structural study has been carried-out by NMR showing a high rigidity for the smaller cycles and a more dynamic behaviour for the largest member of the series. The free energy barrier for the rotational equilibrium for compound 25 is about 3 kcal/mol lower than that calculated for analogous N-tosylated mac…

Sulfonylchemistry.chemical_classificationchemistry.chemical_compoundTosylchemistryStereochemistryOrganic ChemistryDrug DiscoveryAmine gas treatingProtecting groupBiochemistryMedicinal chemistryTetrahedron
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Ferrocene containing chelating ligands 3. Synthesis, spectroscopic characterization, electrochemical behaviour and interaction with metal ions of new…

1995

Abstract Ferrocenecarboxaldehyde reacts with 2-amino-benzoic acid, 2-amino-5-methyl-benzoic acid or 3-amino-2-naphthoic acid to give the corresponding Schiff-base derivatives 2-ferrocenylmethylidenimino-benzoic acid (1), 2-ferrocenylmethylidenimino-5-methyl-benzoic acid (2) and 3-ferrocenylmethylidenimino-2-naphthoic acid (3). 1, 2 and 3 are stable in the solid state but easily hydrolyze in solution. This hydrolysis has been studied kinetically in a methanol-water medium. In order to increase the stability in solution to use these compounds as ligands, the imino group from 1, 2 and 3 was reduced by NaBH4 to give the amino derivatives 2-ferrocenylmethylamino-benzoic acid (4), 2-ferrocenylmet…

Tertiary amineChemistryStereochemistryProtonationCrystal structureMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundHydrolysisPerchlorateMaterials ChemistryAmine gas treatingChelationPhysical and Theoretical ChemistryBenzoic acidInorganica Chimica Acta
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Kemp elimination: a probe reaction to study ionic liquids properties.

2008

The amino induced elimination of benzisoxazole into the relevant o-cyanophenolate ion (Kemp elimination) has been studied in [bmim][BF 4] solution at 298 K. To have information about the interactions between reactants and ionic liquid, the reaction has been carried out at different temperatures (293-313 K). Several primary, secondary, and tertiary amines have been used to study the effect of amine structure on the reaction rate. The collected data show that the amine structure seems to have a crucial role in determining the reaction rate. Furthermore, as different cation or anion structures of an ionic liquid can significantly affect its properties, the title reaction has been performed in …

Tertiary amineOrganic ChemistryInorganic chemistryionic liquids Kemp elimination base catalysisSettore CHIM/06 - Chimica OrganicaMedicinal chemistryPyrrolidineReaction rateSolventchemistry.chemical_compoundchemistryIonic liquidMoleculeAmine gas treatingPiperidineThe Journal of organic chemistry
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Comparative studies of the Pschorr reaction in the pyrazole series. Access to the new dibenzo[e,g]pyrazolo[1,5-a][1,3]diazocine system of pharmaceuti…

2008

The diazonium tetrafluoroborate 11 obtained from 2-amino-N-methyl-N-(1-phenyl-3- methylpyrazol-5-yl)benzamide was transformed in dry acetonitrile via an ionic or radical pathway. Differences were observed with respect to ionic or radical transformations in aqueous media of the analogous diazonium hydrogen sulfate 1 derived from the same amine. In acetonitrile solution, the ionic pathway was characterized by an increased yield of 1,4-dimethyl- 3-phenyl-pyrazolo(3,4-c)isoquinolin-5-one 4 and by the formation of its isomer, the new derivative 7,9-dimethyldibenzo(e,g)pyrazolo(1,5-a)(1,3)diazocin-10(9H)-one 12. When the reaction followed a radical pathway, the pyrazolo(3,4-c)isoquinoline derivat…

Tetrafluoroborate1Ionic bonding4-pyrazolyl transferPyrazoleMedicinal chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPyrazolo[3Organic chemistry4-c]isoquinolineIsoquinolineAcetonitrileBenzamidePyrazolodibenzodiazocinePschorr reactionpyrazolo(34-c)isoquinolinepyrazolodibenzodiazocine14-pyrazolyl transfer X-ray structure14-pyrazolyl transfer; Pschorr reaction; Pyrazolodibenzodiazocine; Pyrazolo[34-c]isoquinoline; X-ray structureOrganic ChemistryPschorr reactionSettore CHIM/08 - Chimica FarmaceuticachemistryPschor reaction pyrazolo[34-c]isoquinoline pyrazolodibenzodiazocine 14- pyrazolyl transfer X-ray structureAmine gas treatingX-ray structureDerivative (chemistry)
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The effect of some amines and alcohols on the organized structure of [bmim][BF4] investigated by 1H NMR spectroscopy

2008

The effect exerted by some amines and alcohols on the 1H NMR spectra of 1-butyl-3- methylimidazolium tetrafluoroborate [bmim][BF4] has been studied. This ionic liquid, which is one of the most widely used, is characterized by a high structural order degree, as a consequence of the symmetry and the coordination ability of the anion. In order to have information about the dependence of the detected effects on the alcohol or amine structure, some different primary, secondary and tertiary amines and alcohols have been considered. Furthermore, in the case of amines, their basicity has been also taken into account. Both amines and alcohols induce variation in chemical shifts values and signal mul…

TetrafluoroborateChemical shiftOrganic ChemistryInorganic chemistryionic liquids 1H NMR measurementsAlcoholSettore CHIM/06 - Chimica Organicachemistry.chemical_compoundchemistryComputational chemistryIonic liquidProton NMRMoleculeAmine gas treatingMultiplicity (chemistry)
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Resorcinarene Podand with Amine-Functionalized Side Arms – Synthesis, Structure, and Binding Properties of a Neutral Anion Receptor

2009

The synthesis and structure of a neutral resorcinarene host bearing four amine-functionalized side arms is described. The anion binding properties were investigated in solution by 1H NMR spectroscopic titration and diffusion experiments and in the gas phase by mass spectrometric studies. It was observed that in solution 1:2 (host/guest) complexes were formed between the resorcinarene host and the basic fluoride and acetate anions, whereas in the gas phase 1:1 complexes with other anions (Cl–, HCOO–, NO3–, and BF4–) were detected additionally. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

TetrafluoroborateStereochemistryOrganic ChemistrySupramolecular chemistryResorcinareneChemical synthesisInclusion compoundchemistry.chemical_compoundchemistryPolymer chemistryTitrationAmine gas treatingPhysical and Theoretical ChemistryAnion bindingEuropean Journal of Organic Chemistry
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