Search results for "Moiety"

showing 10 items of 621 documents

Benzoannulated quinone-type electron acceptors: evolution of the molecular and electronic structures upon reduction

1998

Abstract The molecular and electronic structures of DCNQI and its π-extended derivatives benzo-DCNQI and DCAQI have been investigated using ab initio 6-31G ∗ calculations. The steric hindrance introduced by lateral benzoannulation determines the loss of planarity of the DCNQI moiety for DCAQI. The most stable conformation of DCAQI corresponds to a butterfly-type structure, in which the DCNQI ring adopts a boat conformation and the lateral benzene rings remain planar. This structure lies 2.75 kcal mol −1 below the fully planar conformation. MP2/6-31G ∗ calculations including full geometry optimization confirm the greater stability of the butterfly structure. The geometries of the anions and …

Steric effectschemistry.chemical_classificationChemistryCyclohexane conformationAb initioElectron acceptorCondensed Matter PhysicsRing (chemistry)BiochemistryPlanarity testingCrystallographyAb initio quantum chemistry methodsComputational chemistryMoietyPhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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Intramolecular Nitrone Cycloaddition of α-(Trifluoromethyl)styrenes. Role of the CF3 Group in the Regioselectivity

2017

The intramolecular 1,3-dipolar cycloaddition of ortho-substituted 1,1,1-trifluoromethylstyrene-derived nitrones is described. Tricyclic fused isoxazolidines were obtained as major or exclusive products, in contrast to the case for nonfluorinated substrates, which rendered the bridged derivatives. This change in the regioselectivity was attributed to the electronic and, particularly, steric requirements of the trifluoromethyl group in comparison to the methyl group. It is worth mentioning that trifluoromethylstyrenes have been employed for the first time as dipolarophiles in a 1,3-dipolar intramolecular cycloaddition reaction, leading to the corresponding isoxazolidines bearing a quaternary …

Steric effectschemistry.chemical_classificationTrifluoromethylBicyclic molecule010405 organic chemistryStereochemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesCycloaddition0104 chemical sciencesNitronechemistry.chemical_compoundchemistryIntramolecular forceMoietyThe Journal of Organic Chemistry
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ChemInform Abstract: Ortho-Substituent Effects in N-Arylacetamides. NMR and Molecular Mechanics Investigation.

2010

1H, 13C, 15N and 17O NMR spectra of N-phenylacetamide (acetanilide) and 21 ortho-substituted acetanilides were measured and assigned. The observed NMR parameters are related to the Hammett substituent parameters and conformational characteristics of the acetamido moiety estimated by molecular mechanics calculations. Significant relationships were found for the 13C NMR chemical shifts of C-5 (para to substituent) and the direct spin–spin coupling constant, 1J(C, H), of C-3 (ortho to substituent) with Hammett substituent parameters. For 15N NMR chemical shifts of the amido nitrogen, no general correlation with the Hammett substituent parameters was found. The interactions between functionalit…

Steric effectschemistry.chemical_compoundChemistryChemical shiftSubstituentMoietyGeneral MedicineCarbon-13 NMRResonance (chemistry)Ring (chemistry)Medicinal chemistryAcetanilideChemInform
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Stereoselektive Glycosylierung von Steroidalkoholen mit 2,3,4,6-Tetra-O-privaloyl-α-D-glucopyranosylbromid (Pivalobromglucose) und 2,3,4,6-Tetra-O-(o…

1986

Steroidalkohole verschiedener Struktur, deren Hydroxyfunktionen aus elektronischen und sterischen Grunden in ihrer Reaktivitat differieren und die daruber hinaus empfindliche Gruppierungen enthalten, werden mit 2,3,4,6-Tetra-O-pivaloyl-α-D-glucopyranosylbromid (1) selektiv und effektiv in β-Glucoside ubergefuhrt. Dank des lenkenden Einflusses des 2-O-Pivaloyl-Substituenten wird eine Orthoesterbildung bei den Koenigs-Knorr-Reaktionen stark unterdruckt. Mit dem o-Toluoylrest als Hydroxyschutzgruppe wird diese Lenkung nur in geringem Mas erreicht. Stereoselective Glycosylation of Steroid Alcohols Using 2,3,4,6-Tetra-O-pivaloyl-α-D-glucopyranosyl Bromide (Pivalobromoglucose) and 2,3,4,6-Tetra-O…

Steric effectschemistry.chemical_compoundChemistryStereochemistryBromideOrganic ChemistrySubstituentMoietyStereoselectivityReactivity (chemistry)Nuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryProtecting groupLiebigs Annalen der Chemie
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Crystal structure of N-(tert-butoxycarbonyl)phenylalanyldehydroalanine isopropyl ester (Boc–Phe–ΔAla–OiPr)

2014

In the crystal structure of the de­hydro­dipeptide (Boc-Phe-ΔAla-OiPr), the mol­ecule has a trans configuration of the N-methyl­amide group. Its geometry is different from saturated peptides but is in excellent agreement with other de­hydro­alanine compounds. In the crystal, an N—H⋯O hydrogen bond links the mol­ecules in a herringbone packing arrangement.

Steric effectsde­hydro­alaninecrystal structurede­hydro peptidesCrystal structureResearch Communicationslcsh:Chemistrychemistry.chemical_compoundDehydroalanineαβ-dehydroamino acidsPeptide bondMoietyGeneral Materials ScienceHydrogen bond[alpha]General Chemistrydehydroalaninedehydro peptidesCondensed Matter Physicsherringbone packing[beta]-de­hydro­amino acidsCrystallographyMolecular geometrychemistrylcsh:QD1-999αβ-de­hydro­amino acidsIsopropylActa Crystallographica Section E
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Influence of surface chemistry on the structural organization of monomolecular protein layers adsorbed to functionalized aqueous interfaces.

1993

The molecular organization of streptavidin (SA) bound to aqueous surface monolayers of biotin-functionalized lipids and binary lipid mixtures has been investigated with neutron reflectivity and electron and fluorescence microscopy. The substitution of deuterons (2H) for protons (1H), both in subphase water molecules and in the alkyl chains of the lipid surface monolayer, was utilized to determine the interface structure on the molecular length scale. In all cases studied, the protein forms monomolecular layers underneath the interface with thickness values of approximately 40 A. A systematic dependence of the structural properties of such self-assembled SA monolayers on the surface chemistr…

StreptavidinSurface PropertiesAnalytical chemistrySynthetic membraneBiophysicsBiophysical Phenomenachemistry.chemical_compoundAdsorptionBacterial ProteinsMonolayerMoietyMoleculeAlkylchemistry.chemical_classificationNeutronsAqueous solutionChemistryPhosphatidylethanolaminesProteinsWaterMembranes ArtificialLipidsCrystallographyMicroscopy ElectronCholesterolMicroscopy FluorescenceModels ChemicalAdsorptionStreptavidinDimyristoylphosphatidylcholineResearch ArticleBiophysical journal
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Preparation and protonation of 2-pyrimidyl- and 2-pyrazylpalladium(II) complexes

1985

Abstract The oxidative addition of 2-chloropyrimidine or 2-chloropyrazine to [Pd(PPh 3 ) 4 ] yields a mixture of trans -[PdCl(C 4 H 3 N 2 - C 2 )(PPh 3 ) 2 ] (I) and [PdCl(μ-C 4 H 3 N 2 - C 2 , N 1 )(PPh 3 (II) (C 4 H 3 N 2 = 2-pyrimidyl or 2-pyrazyl group). The mononuclear complexes I are quantitatively converted into the binuclear species II upon treatment with H 2 O 2 . The reaction of II with HCl gives the N -monoprotonated derivatives cis -[PdCl 2 (C 4 H 4 N 2 - C 2 )(PPh 3 )] (III), from which the cationic complexes trans -[PdCl(C 4 H 4 N 2 - C 2 )(L) (L = PPh 3 , IV; PMe 2 Ph, V; PEt 3 , VI) can be prepared by ligand substitution reactions. Reversible proton dissociation occurs in so…

Substitution reactionStereochemistryChemistryLigandOrganic ChemistryProtonationNuclear magnetic resonance spectroscopyBiochemistryOxidative additionInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryProton NMRMoietyPhysical and Theoretical ChemistryTriphenylphosphineJournal of Organometallic Chemistry
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Crystal structure ofp-toluenesulfonylmethyl isocyanide

2015

The molecule of the commercially available title compound, C9H9NO2S, has crystallographically imposed mirror symmetry, the mirror plane passing through the isocyanide group and thepara-C atoms, the methyl C atom and the S atom of the methyl 4-tolyl sulfone moiety. In the crystal, C—H...O hydrogen-bond interactions link the molecules into chains running parallel to thebaxis.

Sulfonylchemistry.chemical_classificationcrystal structureCrystallographyHydrogen bondMethyl isocyanideIsocyanideGeneral ChemistryCrystal structureisocyanide derivativehydrogen bondingCondensed Matter PhysicsBioinformaticsData ReportsSulfoneCrystalCrystallographychemistry.chemical_compoundchemistryQD901-999Physics::Atomic and Molecular ClustersMoietyGeneral Materials SciencePhysics::Atomic PhysicsPhysics::Chemical PhysicsActa Crystallographica Section E Crystallographic Communications
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Bis(2,2'-biphenoxy)borates for electrochemical double-layer capacitor electrolytes.

2010

Fluorine makes the difference! Bis(2,2'-biphenoxy)borates decorated with fluorine substituents have been synthesized and studied in supercapacitor test cells (see scheme). A clear trend towards higher electrochemical stability with the increase of the fluorine content has been observed. For a maximum performance, only two fluorine substituents per benzene moiety are required.

SupercapacitorChemistryOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryElectrolyteElectrochemistryCatalysischemistry.chemical_compoundFluorineMoietyPhenolsBenzeneBoronChemistry (Weinheim an der Bergstrasse, Germany)
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Oxadiazolyl-Pyridinium as Cationic Scaffold for Fluorinated Ionic Liquid Crystals

2021

The synthesis and characterization of a new class of 1,2,4-oxadiazolylpyridinium as a cationic scaffold for fluorinated ionic liquid crystals is herein described. A series of 12 fluorinated heterocyclic salts based on a 1,2,4-oxadiazole moiety, connected through its C(5) or C(3) to an N-alkylpyridinium unit and a perfluoroheptyl chain, differing in the length of the alkyl chain and counterions, has been synthesized. As counterions iodide, bromide and bis(trifluoromethane)sulfonimide have been considered. The synthesis, structure, and liquid crystalline properties of these compounds are discussed on the basis of the tuned structural variables. The thermotropic properties of this series of sa…

TechnologyQH301-705.5QC1-999heterocyclicThermotropic crystalSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni Culturaliionic liquidsfluorinated saltsmesogenschemistry.chemical_compoundliquid crystalsLiquid crystalBromidePolymer chemistryMoietyGeneral Materials ScienceBiology (General)QD1-999InstrumentationAlkylFluid Flow and Transfer Processeschemistry.chemical_classificationTPhysicsProcess Chemistry and TechnologyGeneral EngineeringCationic polymerizationSettore CHIM/06 - Chimica OrganicaEngineering (General). Civil engineering (General)Computer Science ApplicationsChemistrychemistryddc:540Ionic liquidPyridiniumTA1-2040Applied Sciences
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