Search results for "Meisenheimer complex"

showing 3 items of 3 documents

Anionic Organic Guests Incorporated in Zeolites: Adsorption and Reactivity of a Meisenheimer Complex in Faujasites

2005

Zeolites are suitable microporous hosts for positively charged organic species, but it is believed that they cannot adsorb organic anions. Pure Meisenheimer complex, derived from reduction of 2,4-dinitroaniline with NaBH4, was adsorbed inside faujasite cavities. Evidence for the internal incorporation of this negatively charged reaction intermediate comes from 1) XPS elemental analysis as a function of the depth of penetration into the particle, 2) the remarkable blue shift in lambda(max) of the Meisenheimer complex adsorbed on zeolite (ca. 470 nm) as compared to that in acetonitrile (580 nm) and 3) from the lack of reactivity with size-excluded hydride-acceptor reagents. Evidence is provid…

AnionsAniline CompoundsMolecular StructurebiologyChemistryOrganic ChemistryInorganic chemistryGeneral ChemistryReaction intermediateMicroporous materialFaujasiteengineering.materialCatalysisMeisenheimer complexAdsorptionZeolitesbiology.proteinengineeringReactivity (chemistry)AdsorptionZeoliteOxidation-ReductionOrganic anionChemistry - A European Journal
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2020

Electrophilic (het)arenes can undergo reactions with nucleophiles yielding π- or Meisenheimer (σ-) complexes or the products of the SNAr addition/elimination reactions. Such building blocks have only rarely been employed for the design of enzyme inhibitors. Herein, we demonstrate the combination of a peptidic recognition sequence with such electrophilic (het)arenes to generate highly active inhibitors of disease-relevant proteases. We further elucidate an unexpected mode of action for the trypanosomal protease rhodesain using NMR spectroscopy and mass spectrometry, enzyme kinetics and various types of simulations. After hydrolysis of an ester function in the recognition sequence of a weakly…

StereochemistryCarboxylic acidmedicine.medical_treatmentPharmaceutical Science010402 general chemistry01 natural sciencesAnalytical ChemistryNucleophileNucleophilic aromatic substitutionDrug DiscoverymedicineEnzyme kineticsPhysical and Theoretical Chemistrychemistry.chemical_classificationProteasebiology010405 organic chemistryOrganic ChemistryActive siteCysteine proteaseMeisenheimer complex0104 chemical scienceschemistryChemistry (miscellaneous)biology.proteinMolecular MedicineMolecules
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CF3: An Electron-Withdrawing Substituent for Aromatic Anion Acceptors? “Side-On” versus “On-Top” Binding of Halides

2016

The ability of multiple CF3 -substituted arenes to act as acceptors for anions is investigated. The results of quantum-chemical calculations show that a high degree of trifluoromethyl substitution at the aromatic ring results in a positive quadrupole moment. However, depending on the polarizability of the anion and on the substitution at the arene, three different modes of interaction, namely Meisenheimer complex, side-on hydrogen bonding, or anion-π interaction, can occur. Experimentally, the side-on as well as a η(2) -type π-complex are observed in the crystal, whereas in solution only side-on binding is found.

Trifluoromethyl010405 organic chemistryHydrogen bondChemistryStereochemistryOrganic Chemistryanion acceptorsSubstituentGeneral ChemistryCrystal structureCF3-substituted arenes010402 general chemistryRing (chemistry)01 natural sciencesCatalysisMeisenheimer complex3. Good health0104 chemical sciencesCrystallographychemistry.chemical_compoundPolarizabilityPolar effectta116Chemistry: A European Journal
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