Search results for "ammonium"

showing 10 items of 1070 documents

Weak interactions between resorcinarenes and diquaternary alkyl ammonium cations

2005

The interactions of resorcin[4]arenes 1 with alkyl ammonium cations bearing a 1,4-diazabicyclo[2.2.2]octane (DABCO) scaffold (32+, 42+ and 52+) were analyzed in the solid state by X-ray crystallography, in solution by 1H NMR spectroscopy, and in the gas phase by ESI-TOF mass spectrometry. The results are complemented with AM1 calculations and compared to previous reports on complexation studies of resorcinarenes with quaternary alkyl ammonium cations. The NMR titration results indicate that there are hardly any differences in the binding of the quaternary tetramethyl ammonium cation 2+ and the diquaternary N,N’-dimethyl DABCO dication 42+. The large N,N’-dibenzyl DABCO dication 52+ has two …

chemistry.chemical_classificationArylInorganic chemistryCationic polymerizationGeneral ChemistryDABCOMass spectrometryMedicinal chemistryCatalysisDicationchemistry.chemical_compoundchemistryMaterials ChemistryAmmoniumAlkylOctaneNew J. Chem.
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ChemInform Abstract: Ring Expansion of 1,2,3,4-Tetrahydroisoquinolines to Dibenzo[c,f]azonines. An Unexpected [1,4]-Sigmatropic Rearrangement of Nitr…

2014

When the products of a Strecker reaction of 1,2,3,4-tetrahydroisoquinolines with aromatic aldehydes are quaternized with alkyl triflates and subsequently treated with base, a ring expansion to 6,7,8,13-tetrahydro-5H-dibenzo[c,f]azonine-5-carbonitriles takes place. The nine-membered cyclic products can be obtained in good yields (78–89%) in a process involving the [1,4]-sigmatropic rearrangement of a nitrile-stabilized ammonium ylide. The reaction sequence provides a new, simple, and efficient method for the synthesis of these unusual N-heterocycles.

chemistry.chemical_classificationBase (chemistry)NitrileStereochemistryStrecker amino acid synthesisGeneral MedicineSigmatropic reactionRing (chemistry)Medicinal chemistrychemistry.chemical_compoundchemistryYlideAmmoniumAlkylChemInform
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Synthesis and Unusual NMR-Spectroscopic Behavior of a Strained Bicyclic Ammonium Salt

2018

chemistry.chemical_classificationBicyclic molecule010405 organic chemistryChemistryOrganic ChemistrySalt (chemistry)Nuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundX-ray crystallographyAmmoniumPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Synthesis of cyanoacetic acid by carbon dioxide and electrogenerated acetonitrile anion in undivided cells equipped with sacrificial anodes

2008

The electrochemical synthesis of cyanoacetic acid was performed by cathodic reduction of tetraalkylammonium salts (R4NX) in acetonitrile in undivided cells equipped with sacrificial anodes with concomitant or subsequent addition of carbon dioxide. These syntheses avoid the use of dangerous reagents, yield cyanoacetic acid in moderate faradic yields and confirm that the cathodic reduction of tetraalkylammonium salts in the presence of acetonitrile leads to the formation of the anion CNCH2-.

chemistry.chemical_classificationCHLOROACETONITRILE electrocarboxylationNitrileSupporting electrolyteGalvanic anodecathodic reduction of alkyl ammonium saltsGeneral Chemical EngineeringCarboxylic acidInorganic chemistrycarbon dioxideSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryAnalytical Chemistrychemistry.chemical_compoundsupporting electrolyteSettore ING-IND/22 - Scienza E Tecnologia Dei Materialialkyl ammonium saltCyanoacetic acidchemistryReagentElectrochemistrycyanoacetic acidAcetonitrilesacrificial anodeJournal of Electroanalytical Chemistry
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Speciation of chitosan-phosphate and chitosan-nucleotide systems in an NaCl aqueous solution

2010

AbstractThe speciation of chitosan (310 kDa) with organic (adenosine 5’-monophosphate, AMP, and adenosine 5’-triphosphate, ATP), and inorganic phosphorus containing ligands (phosphate and pyrophosphate) was investigated in NaCl aqueous solutions at I = 0.1mol L−1 and T = 25°C. For all the systems, the investigated results obtained gave evidence for the formation of (chitosan)LHi complex species (L = nucleotides, phosphate and pyrophosphate; i = 1 to 4, but for AMP, i = 1 to 3). The stability data of complex species were used to calculate the sequestering ability of chitosan towards phosphorus compounds considered here, expressed as pL50 i.e., – log(total chitosan concentration) necessary to…

chemistry.chemical_classificationChemical Health and SafetyAqueous solutionChemistryLigandHealth Toxicology and MutagenesisPhosphorusInorganic chemistrychemistry.chemical_elementToxicologyPhosphatePyrophosphateAdenosineChitosanchemistry.chemical_compoundchitosan nucleotides phosphorus containing ligands chemical speciation polyammonium-phosphate interaction polyammonium-nucleotide interactionmedicineNucleotideSettore CHIM/01 - Chimica Analiticamedicine.drug
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Isolation of enantiomerically pure organometallic palladium compounds: synthesis of the triangles prepared from enantiopure [cis-Pd2(C6H4PPh2)2(NCCH3…

2009

Reaction of the racemic [Pd(C(6)H(4)PPh(2))Br](4) () with the silver salt of 1R-(1alpha,2beta,3alpha)]-3-methyl-2-(nitromethyl)-5-oxocyclopentaneacetate, (R)-AgO(2)CR*, results in the formation of a mixture of diastereoisomers (RRR)- and (SRR)- of the formula Pd(2)(C(6)H(4)PPh(2))(2)(O(2)CR*)(2) that were separated by standard chromatographic methods. Each diastereoisomer was readily converted into the tetrametallic stereoisomers (SS)- and (RR)-, of the formula [Pd(C(6)H(4)PPh(2))Br](4) that were isolated and characterized by X-ray crystallography. The R enantiomer of the solvated cationic species [cis-Pd(2)(C(6)H(4)PPh(2))(2)(NCCH(3))(4)](2+), obtained from (RR)-, was reacted with ammonium…

chemistry.chemical_classificationChemistryStereochemistryCationic polymerizationDiastereomerSalt (chemistry)chemistry.chemical_elementInorganic Chemistrychemistry.chemical_compoundEnantiopure drugAmmonium31p nmr spectroscopyEnantiomerPalladiumDalton Transactions
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Der (2-Phenyl-2-trimethylsilyl)ethyl-(PTMSE)-Ester – eine neutral spaltbare Carboxyschutzgruppe/The (2-Phenyl-2-trimethylsiylyl)ethyl (PTMSE) Ester –…

2002

(2-Phenyl-2-trimethylsilyl)ethyl (PTMSE) esters of aminoacids and peptides are stable under the conditions of hydrogenolytic cleavage of benzoxycarbonyl(Z) and benzyl ester groups, base-induced removal of Fmoc groups, palladium(0)-catalyzed removal of allyloxycarbonyl (Aloc) and even acidolytic cleavage of Boc groups. PTMSE esters are also stable under the conditions of peptide condensation reactions. The PTMSE ester is selectively cleaved by treatment with tetrabutylammonium fluoride (TBAF) trihydrate in dichloromethane, i. e. under almost neutral conditions, within a few minutes and, therefore, considered a valuable novel carboxy protecting group.

chemistry.chemical_classificationChemistrychemistry.chemical_elementPeptideGeneral ChemistryCondensation reactionCleavage (embryo)Tetrabutylammonium fluorideMedicinal chemistrychemistry.chemical_compound(2-Phenyl-2-trimethylsilyl)ethylProtecting groupPalladiumDichloromethaneZeitschrift für Naturforschung B
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Hydrophobicity of Ionizable Compounds. A Theoretical Study and Measurements of Diuretic Octanol−Water Partition Coefficients by Countercurrent Chroma…

1999

Countercurrent chromatography was used to determine the octanol−water partition coefficients (Po/w) of 23 diuretic drugs. The measured Po/w values ranged over 4 orders of magnitude from 0.05 to 550 (−1.3 < log Po/w < +2.7). All the compounds, except spironolactone, were ionizable. The Po/w values were strongly depending on the aqueous-phase pH. A theoretical model linking these values with the pH was derived for four cases:  (i) molecular acid−anionic base, (ii) cationic acid−molecular base, (iii) biprotic systems with two acidic or basic groups showing the same charge sign, and (iv) biprotic systems with ionizable groups showing different charges with special attention to the amino acid ca…

chemistry.chemical_classificationChromatographyBase (chemistry)Ammonium phosphateCarboxylic acidCationic polymerizationAnalytical chemistryAnalytical ChemistryPartition coefficientchemistry.chemical_compoundCountercurrent chromatographychemistryAmine gas treatingIonic compoundAnalytical Chemistry
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Influence of the presence of surfactants and humic acid in waters on the indophenol-type reaction method for ammonium determination.

2005

Abstract This work has evaluated the influence of humic acid and/or surfactants in the quantification of ammonium in waters with the indophenol-type reaction method. Thymol has been employed with the colorimetric method for sample ammonium concentrations between 0.25 and 1 mg L −1 . In addition, SPE/diffuse reflectance method has been used for quantification of ammonium at low concentrations (between 0.025 and 0.25 mg L −1 ). Matrix effect owing to humic substances were observed with the colorimetric method when the concentration was equal or higher than 25 mg L −1 . Lower concentrations of humic compounds produced matrix effects with the more sensitive SPE/diffuse reflectance method. Gener…

chemistry.chemical_classificationChromatographyCationic polymerizationcomplex mixturesColorimetry (chemical method)Analytical Chemistrychemistry.chemical_compoundchemistryStandard additionHumic acidAmmoniumSolid phase extractionIndophenolDerivatizationTalanta
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Effect of the hydrophobic spacer in bonded [Cu(l-hydroxyprolyl)alkyl]+ silicas on retention and enantioselectivity of α-amino acids in high-performan…

1983

Abstract The following chiral ligands were bonded to silica: [Cu( l -hydroxyprolyl)methyl) + on LiChrosorb Si 60 (1), [Cu( l -hydroxyprolyl)methyl] + on LiChrosorb Si 100 (2) and [Cu( l -hydroxyprolyl) n -octyl] + on LiChrosorb Si 100 (3). The packings contained residual iodomethyl- and ω-iodooctyl groups at the surface. Studies on packing 1 and 2 under comparable conditions in eluents containing 10 -4 M copper acetate showed a higher retention on 1 than on 2 but a much better enantioselectivity in the latter case. The retention of enantiomers on all packings examined was found to be governed by the eluent pH and methanol content as well as by the concentration of ammonium acetate. The vari…

chemistry.chemical_classificationChromatographyChemistryOrganic Chemistrychemistry.chemical_elementGeneral MedicineBiochemistryHigh-performance liquid chromatographyCopperAnalytical ChemistryHydrophobic effectchemistry.chemical_compoundColumn chromatographyMethanolEnantiomerAmmonium acetateAlkylJournal of Chromatography A
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