Search results for "Trifluoroacetic Acid"

showing 10 items of 34 documents

Evaluation of methods aimed at complete removal of template from molecularly imprinted polymers

2001

Polymers imprinted with clenbuterol were used to study the influence of various post-polymerization treatments [e.g., thermal annealing, microwave assisted extraction (MAE), Soxhlet extraction and supercritical fluid template desorption] on the bleeding of residual template. The aim of the study was to reduce the bleeding to levels that would allow the use of the materials as affinity phases for extraction of clenbuterol from bovine urine at concentrations below 1 ng ml−1. After treatment, the clenbuterol imprinted polymers were packed into solid-phase extraction columns and the bleeding was estimated by quantifying the amount of template released in 10 ml of methanol–acetic acid (9 + 1 v/v…

Formic acidENANTIOMERSCHROMATOGRAPHYBiochemistryAnalytical Chemistrychemistry.chemical_compoundElectrochemistrymedicineTrifluoroacetic acidSOLUTE RETENTIONEnvironmental ChemistrySolid phase extractionSpectroscopyChromatographyChemistryElutionExtraction (chemistry)Molecularly imprinted polymerSTATIONARY PHASESCHIRAL CAVITIESSupercritical fluidSOLID-PHASE EXTRACTIONRESOLUTIONClenbuterolENRICHMENTSORBENTmedicine.drug
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Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors

2021

Abstract Neutral halogen‐bonded O−I−N complexes were prepared from in situ formed carbonyl hypoiodites and aromatic organic bases. The carbonyl hypoiodites have a strongly polarized iodine atom with larger σ‐holes than any known uncharged halogen bond donor. Modulating the Lewis basicity of the selected pyridine derivatives and carboxylates leads to halogen‐bonded complexes where the classical O−I⋅⋅⋅N halogen bond transforms more into a halogen‐bonded COO−⋅⋅⋅I−N+ ion‐pair (salt) with an asymmetric O−I−N moiety. X‐ray analyses, NMR studies, and calculations reveal the halogen bonding geometries of the carbonyl hypoiodite‐based O−I−N complexes, confirming that in the solid‐state the iodine at…

Halogen Bondingpyridineinorganic chemicalsHalogen bondOrganic basehalogeenitCommunicationSupramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyGeneral MedicinehypoioditeMedicinal chemistryCatalysisCommunicationssupramolecular chemistrychemistry.chemical_compoundkemialliset sidoksetNMR spectroscopychemistryPyridineTrifluoroacetic acidsupramolekulaarinen kemiaMoietyCarboxylateAngewandte Chemie
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Inhibition of imidazolidinone intermediate formation in the aldol reactions catalyzed by zinc–prolinamide complexes

2011

Abstract The use of zinc salts as cocatalysts in aldol condensations catalyzed by single prolinamide (and in the extension by other more complex prolinamides) can prevent the formation of the parasitic intermediate imidazolidinone, with faster and also more stereoselective reactions than those catalyzed by the free amine. This new finding, together with this ion’s already known properties, make zinc salts highly suitable additives for aldol reactions catalyzed for prolinamide derivatives.

ImidazolidinoneOrganic Chemistrychemistry.chemical_elementZinc saltsZincBiochemistryCombinatorial chemistryCatalysischemistry.chemical_compoundchemistryAldol reactionDrug DiscoveryTrifluoroacetic acidOrganic chemistryStereoselectivityAmine gas treatingTetrahedron
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In vitro evaluation of poloxamer in situ forming gels for bedaquiline fumarate salt and pharmacokinetics following intramuscular injection in rats

2019

Graphical abstract

In situPO Propylene oxideIV IntravenousP338 Poloxamer 338lcsh:RS1-441Pharmaceutical Sciencechemistry.chemical_compoundn Sample sizeSD Standard deviationIM Intramuscularchemistry.chemical_classificationC0 Analyte plasma concentration at time zeroDoE Design of experimentsUV UltravioletPharmacology. TherapyK2.EDTA Potassium ethylenediaminetetraacetic acidLC–MS/MS Liquid chromatography-tandem mass spectrometryH&E Hematoxylin and eosintmax Sampling time to reach the maximum observed analyte plasma concentrationIn situ forming gelsCMC Critical micellar concentrationCmax Maximum observed analyte plasma concentrationIntramuscular injectionDN Dose normalizedGPT Gel point temperaturePLGA Poly-(DL-lactic-co-glycolic acid)TFA Trifluoroacetic acidCAN AcetonitrileATP Adenosine 5′ triphosphateSalt (chemistry)Polyethylene glycolPoloxamerArticlelcsh:Pharmacy and materia medicaPharmacokineticsIn vivoUHPLC Ultra-high performance liquid chromatographyPharmacokineticsAUClast Area under the analyte concentration versus time curve from time zero to the time of the last measurable (non-below quantification level) concentrationEO Ethylene oxideNMP N-methyl-2-pyrrolidoneComputingMethodologies_COMPUTERGRAPHICSAUC∞ Area under the analyte concentration vs time curve from time zero to infinite timeP407 Poloxamer 407In vitro releasePoloxamerCMT Critical micellar temperatureGel erosionIn vitrot1/2 Apparent terminal elimination half-lifechemistryMDR-TB Multi-drug resistant tuberculosisAUC80h Area under the analyte concentration versus time curve from time zero to 80 htlast Sampling time until the last measurable (non-below quantification level) analyte plasma concentrationMRM Multiple reaction monitoringNuclear chemistrySustained releaseInternational Journal of Pharmaceutics: X
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Der 1,3‐Dithian‐2‐ylmethoxycarbonyl‐(Dmoc)‐Rest als Zweistufen‐Schutzgruppe für die Aminofunktion von Aminosäuren und Peptiden

1982

Der 1,3-Dithian-2-ylmethoxycarbonyl-(Dmoc)-Rest (4) als Schutzgruppe fur die Aminofunktion ist gegen Basen und gegen Trifluoressigsaure stabil. Peptidsynthesen mit Dmoc-Aminosauren werden nach dem Mischanhydrid- und nach dem modifizierten Carbodiimid-Verfahren durchgefuhrt. Zur Abspaltung der Dmoc-Schutzgruppe wird diese mit Peressigsaure am Schwefel oxidiert (z. B. zu 13, 14). Die dabei gebildete CH-acide Form kann unter milden basischen Bedingungen von der blockierten Aminofunktion abgelost werden. The 1,3-Dithian-2-ylmethoxycarbonyl (Dmoc) Group as Two-Step Amino Protective Function in Peptide Chemistry The 1,3-dithian-2-ylmethoxycarbonyl (Dmoc) group (4) as amino protective function is …

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundChemistryStereochemistryTrifluoroacetic acidPeptide chemistryMoietyPeptideCarbodiimideChemische Berichte
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Formation and Reactivity of the [Cp‘2Ta(H)2]+ Cation (Cp‘ = η5-tBuC5H4)

1999

The complex Cp‘2Ta(H)(OCOCF3)2 (2) is synthesized by the acidolysis of Cp‘2TaH3 (1) (Cp‘ = η5-tBuC5H4) in the presence of an excess of trifluoroacetic acid. 1 undergoes a loss of H- upon the reacti...

Inorganic Chemistrychemistry.chemical_compoundChemistryOrganic ChemistryTrifluoroacetic acidReactivity (chemistry)Physical and Theoretical ChemistryMedicinal chemistryOrganometallics
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Formation and Reactivity of a Tantalocene Trihydride Containing an Aminoethyl‐Functionalised Ligand

2003

The complex [Cp*{C5H4(CH2CH2NMe2)}TaCl2] (1) was synthesised by reaction of the lithium salt LiC5H4(CH2CH2NMe2) with the tantalum compound [Cp*TaCl3(PMe3)]. Reduction of 1 with NaAl(H)2(OCH2CH2OMe)2 leads to the trihydride derivative [Cp*{C5H4(CH2CH2NMe2)}TaH3] (2). The oxidation of 2 in THF with ferrocenium ion leads to a cationic dihydride intermediate [Cp*{C5H4(CH2CH2NMe2)}TaH2]PF6 (3) with an intramolecular stabilization by the aminoethyl side-chain of the cyclopentadienyl ligand. The hemilabile character of the functionalised cyclopentadienyl ligand was checked by treating 3 with electron-donating ligands (e.g. phosphanes, sulfides, anions); in all cases, no displacement of the amino g…

Inorganic Chemistrychemistry.chemical_compoundchemistryCyclopentadienyl complexStereochemistryHydrideLigandTrifluoroacetic acidReactivity (chemistry)Crystal structureMedicinal chemistryDerivative (chemistry)AdductEuropean Journal of Inorganic Chemistry
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Hydrogen bond-mediated conjugates involving lanthanide diphthalocyanines and trifluoroacetic acid (Lnpc2@TFA): Structure, photoactivity, and stability

2020

The interaction between lanthanide diphthalocyanine complexes, LnPc2 (Ln = Nd, Sm, Eu, Gd, Yb, Lu

LanthanideTFA conjugatePharmaceutical Science010402 general chemistryPhotochemistryphotostability01 natural sciencessinglet oxygenAnalytical Chemistrylcsh:QD241-441lanthanide diphthalocyanineschemistry.chemical_compoundUV-Vis spectralcsh:Organic chemistryTFA conjugatesDrug DiscoveryTrifluoroacetic acidMoleculePhysical and Theoretical Chemistrylanthanide diphthalocyanine010405 organic chemistryHydrogen bondSinglet oxygenOrganic Chemistryphoton upconversionChromophore0104 chemical scienceschemistryChemistry (miscellaneous)PhthalocyanineMolecular MedicineDensity functional theoryMolecules
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[(11)C]PR04.MZ, a promising DAT ligand for low concentration imaging: Synthesis, efficient (11)C-O-methylation and initial small animal PET studies.

2009

PR04.MZ was designed as a highly selective dopamine transporter inhibitor, derived from natural cocaine. Its binding profile indicates that [{sup 11}C]PR04.MZ may be suited as a PET radioligand for the non-invasive exploration of striatal and extrastriatal DAT populations. As a key feature, its structural design facilitates both, labelling with fluorine-18 at its terminally fluorinated butynyl moiety and carbon-11 at its methyl ester function. The present report concerns the efficient [{sup 11}C]MeI mediated synthesis of [{sup 11}C]PR04.MZ from an O-desmethyl precursor trifluoroacetic acid salt with Rb{sub 2}CO{sub 3} in DMF in up to 95 {+-} 5% labelling yield. A preliminary {mu}PET-experim…

MaleBiodistributionFluorine RadioisotopesTime FactorsStereochemistryClinical BiochemistryPharmaceutical ScienceBiochemistryChemical synthesisMethylationRats Sprague-Dawleychemistry.chemical_compoundRadioligand AssayDrug DiscoveryRadioligandTrifluoroacetic acidMoietyAnimalsMolecular BiologyDopamine transporterCarbon IsotopesDopamine Plasma Membrane Transport ProteinsbiologyBicyclic moleculeOrganic ChemistryBrainLigand (biochemistry)Magnetic Resonance ImagingRatschemistryModels ChemicalDrug DesignPositron-Emission Tomographybiology.proteinMolecular MedicineAzabicyclo CompoundsTropanesBioorganicmedicinal chemistry letters
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Experimental and Computational Studies of Hydrogen Bonding and Proton Transfer to [Cp*Fe(dppe)H]

2005

The present contribution reports experimental and computational investigations of the interaction between [Cp*Fe(dppe)H] and different proton donors (HA). The focus is on the structure of the proton transfer intermediates and on the potential energy surface of the proton transfer leading to the dihydrogen complex [Cp*Fe(dppe)(H2)]+. With p-nitrophenol (PNP) a UV/Visible study provides evidence of the formation of the ion-pair stabilized by a hydrogen bond between the nonclassical cation [Cp*Fe(dppe)(H2)]+ and the homoconjugated anion ([AHA]-). With trifluoroacetic acid (TFA), the hydrogen-bonded ion pair containing the simple conjugate base (A-) in equilibrium with the free ions is observed…

Models MolecularSpectrophotometry InfraredProtonPropanolsIronInfrared spectroscopyLigands010402 general chemistryPhotochemistrySensitivity and Specificity01 natural sciencesPolarizable continuum modelCatalysisNitrophenolschemistry.chemical_compoundHydride ligandOrganometallic CompoundsTrifluoroacetic acidMoleculeDihydrogen bondingComputer Simulation[CHIM.COOR]Chemical Sciences/Coordination chemistry10. No inequalityMolecular Structure010405 organic chemistryHydrogen bondChemistryOrganic ChemistryProton transfer mechanismHydrogen BondingGeneral Chemistry0104 chemical sciencesQuantum TheoryThermodynamicsPhysical chemistrySpectrophotometry UltravioletDFT CalculationsDihydrogen complexProtonsSolvent effects
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