Search results for "Proton"

showing 10 items of 5886 documents

Conjugate addition of organolithium reagents to α,β-unsaturated carboxylic acids

1999

Abstract Conjugate addition of primary, secondary, tertiary alkyl and phenyl lithium reagents to 2-alkenoic acids affords good yields of branched saturated carboxylic acids. Methyl groups at the α- and β-carbon of the 2-alkenoic acid decrease reactivity as acceptors, and foster deprotonation, respectively. The lithium enediolate resulting from the conjugate addition can react with electrophiles. PM3 calculations are in agreement with the substituent effects.

chemistry.chemical_classificationOrganic ChemistrySubstituentchemistry.chemical_elementBiochemistryMedicinal chemistrychemistry.chemical_compoundDeprotonationchemistryReagentDrug DiscoveryElectrophileLithiumReactivity (chemistry)AlkylConjugateTetrahedron
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Macrocyclic (1,3)- and (1,4)-benzena-(1,4)-piperazinacyclophanes

1995

New large, up to 45-membered macrocycles were synthesised from piperazine and m- and p-2,6-bis(bromomethyl)xylene under high dilution conditions. X-ray structures of compounds 3a, 4a, 5a, and 8b were determined. Surprisingly, none of the macrocycles prepared showed any inclusion properties towards small guest molecules. Instead, the compounds were found to self-organize during the packing process into larger structures due to the complementary of the molecular skeletons. In the crystalline state 3a forms nets, where the macrocycles are bound by HCH…N interactions to each other. 4a exits in a dimeric structure, which, in turn, further extends to a sheet structure. The positively charged phan…

chemistry.chemical_classificationOrganic ChemistryXyleneSalt (chemistry)ProtonationGeneral ChemistryTurn (biochemistry)Piperazinechemistry.chemical_compoundCrystallographychemistrySheet structureMoleculeSelf-assemblyPhysical and Theoretical ChemistryLiebigs Annalen
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Modified photobehavior of carboxylic acid derivatives induced by protonation

1987

Abstract A series of carboxylic acid derivatives 1–6 containing a second interacting function have been converted into the corresponding O -protonated species or acylium ions upon treatment with 96% sulfuric acid or oleum, respectively, at room temperature. The resulting stable cations have been spectroscopically characterized and submitted to irradiation. Cis-trans photoisomerization was observed in the ionic speciesderived from trans -crotonic, fumaric and maleic acids, and maleic anhydride. By contrast protonated crotonolactone 5a+ was found to be photostable. Finally, protonated α-bromobutyrolactone 6a+ was clean and efficiently dehydrohalogenated to 5a+ upon irradiation. Since the norm…

chemistry.chemical_classificationPhotoisomerizationChemistryCarboxylic acidOrganic ChemistryMaleic anhydrideSulfuric acidProtonationBiochemistryMedicinal chemistryCis trans isomerizationOleumchemistry.chemical_compoundDrug DiscoveryOrganic chemistryAliphatic compoundTetrahedron
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Measurements of ν̅ μ and ν̅ μ + ν μ charged-current cross-sections without detected pions or protons on water and hydrocarbon at a mean anti-neutrino…

2021

Abstract We report measurements of the flux-integrated ν̅μ and ν̅μ + νμ charged-current cross-sections on water and hydrocarbon targets using the T2K anti-neutrino beam with a mean beam energy of 0.86 GeV. The signal is defined as the (anti-)neutrino charged-current interaction with one induced $\mu^\pm$ and no detected charged pion or proton. These measurements are performed using a new WAGASCI module recently added to the T2K setup in combination with the INGRID Proton Module. The phase space of muons is restricted to the high-detection efficiency region, $p_{\mu}>400~{\rm MeV}/c$ and $\theta_{\mu}<30^{\circ}$, in the laboratory frame. An absence of pions and protons in the …

chemistry.chemical_classificationPhysicsParticle physicsMuonProton010308 nuclear & particles physicsGeneral Physics and Astronomy01 natural sciencesHydrocarbonPionchemistry0103 physical sciences010306 general physicsNucleonEnergy (signal processing)Charged currentBar (unit)Progress of Theoretical and Experimental Physics
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1H,13C and17O NMR spectroscopic study of four bicyclo [3.1.1]heptenes (derivatives of α-pinene) and four bicyclo[3.1.1]heptanes (derivatives of β-pin…

1992

Four derivatives of 2, 6, 6-trimethylbicyclo[3.1.1]hept-2-ene (α-pinene) and four derivatives of 2-methylene-6, 6-dimethylbicyclo[3.1.1]heptane (β-pinene) were synthesized and their 1H, 13C and 17O NMR spectra were measured, analysed and assigned. The 1H NMR spectral parameters were obtained by computer-aided analyses of the very complex multi-spin, second-order spectra. Some of the 13C NMR chemical shift assignments of these compounds reported in the literature should be changed, based on these accurate 1H NMR spectral analyses and carbon-proton chemical shift correlated spectra (COSY). The new assignments are supported by the 1J(C, H) values, which show a strong dependence on the bond ang…

chemistry.chemical_classificationPineneHeptaneKetoneBicyclic moleculeStereochemistryGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRchemistry.chemical_compoundCrystallographyMolecular geometrychemistryProton NMRGeneral Materials ScienceMagnetic Resonance in Chemistry
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Supramolecular Nanocycles Comprisingβ-Cyclodextrin-click-Ferrocene Units: Rings of Rings of Rings

2010

We applied 1,3-dipolar cycloaddition to bind ethynylferrocene onto 6I-azido-6I-deoxycyclomaltoheptaose under microwave assisted conditions. The process was investigated by (1) H NMR, FT-IR spectroscopy, and MALDI-TOF mass spectrometry. The ability of the synthesized compound to self-organize to cyclic supramolecular structures was investigated by dynamic light scattering measurements and cryo-transmission electron microscopy.

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinOrganic ChemistrySupramolecular chemistrymacromolecular substancesCycloadditionInclusion compoundchemistry.chemical_compoundchemistryFerrocenePolymer chemistry13-Dipolar cycloadditionMaterials ChemistryProton NMROrganic chemistryMetalloceneMacromolecular Rapid Communications
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Synthesis and characterisation of novel chemical conjugates based on alpha, beta-polyaspartylhydrazide and beta-cyclodextrins

2006

A new family of supramolecular systems based on a synthetic polyaminoacid and cyclic oligosaccharides such as beta-cyclodextrins (beta-CDs) was synthesised. The pharmaceutical potential of these systems arises from the proper combination between the complexing properties of cyclodextrins and the particular pharmacokinetic profile that can be obtained by using macromolecular conjugates with a biocompatible backbone. Five supramolecular conjugates were synthesised by using alpha,beta-polyaspartylhydrazide (PAHy) as a polymeric component and various amounts of two P-CD derivatives. In particular, by reaction of PAHy with beta-CD monoaldehyde, samples named as A(1), A(2) and A(3), bearing, resp…

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinsupramolecular systemsOrganic ChemistrySupramolecular chemistryGeneral Physics and AstronomyChemical modificationConjugated systemCombinatorial chemistryInclusion compoundbeta-cyclodextrinchemistry.chemical_compoundchemistryMaterials ChemistryProton NMROrganic chemistryPAHyMacromoleculeConjugate
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Rapid Synthesis and MALDI-ToF Characterization of Poly(ethylene oxide) Multiarm Star Polymers

2009

Multiarm PEO star polymers with a purely aliphatic polyether structure have been synthesized using hyperbranched polyglycerol (PG) with different molecular weights as a multifunctional initiator. Different degrees of deprotonation of the initiator were studied with respect to molecular weight control. The results show that the degree of deprotonation is a crucial parameter for the synthesis of well-defined polymers with controlled molecular weights. Partial deprotonation of the PG hydroxyl groups (5-8%) was proven to represent an optimum for the synthesis of star polymers with molecular masses close to the theoretical values. Molecular weights of the stars ranged between 9 000 and 30000g · …

chemistry.chemical_classificationPolymers and PlasticsMolecular massChemistryOrganic ChemistryOxidePolymerCondensed Matter PhysicsRing-opening polymerizationchemistry.chemical_compoundAnionic addition polymerizationDeprotonationPolyolDendrimerPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Poly(1,2-glycerol carbonate): A Fundamental Polymer Structure Synthesized from CO2 and Glycidyl Ethers

2013

The functional, aliphatic poly(1,2-glycerol carbonate) as a fundamental, simple polymer structure based on glycerol and CO2 was prepared by combination of glycidyl ether monomers with carbon dioxide via two different approaches. The material was obtained by two-step procedures either via copolymerization of (i) ethoxy ethyl glycidyl ether (EEGE) or (ii) benzyl glycidyl ether (BGE) with CO2, followed by removal of the respective protecting groups via acidic cleavage for (i) and hydrogenation for (ii). The resulting protected polycarbonate structures and the targeted poly(1,2-glycerol carbonate) were investigated with 1H NMR and 13C NMR spectroscopy as well as 2D-NMR methods. Removal of both …

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryPolymerInorganic Chemistrychemistry.chemical_compoundMonomerchemistryvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumGlycerolCopolymerAlkoxy groupProton NMRCarbonateOrganic chemistryPolycarbonateMacromolecules
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N,N-Diallylglycidylamine: A Key Monomer for Amino-Functional Poly(ethylene glycol) Architectures

2012

The first application of N,N-diallylglycidylamine (DAGA) as a monomer for anionic ring-opening polymerization is presented. The monomer is obtained in a one-step procedure using epichlorohydrin and N,N-diallylamine. Both random and block copolymers consisting of poly(ethylene glycol) and poly(N,N-diallylglycidylamine) with adjusted DAGA ratios from 2.5 to 24% have been prepared, yielding well-defined materials with low polydispersities (Mw/Mn) in the range 1.04–1.19. Molecular weights ranged between 2600 and 10 300 g mol–1. Isomerization of allylamine to enamine structures during polymerization depending on time, temperature, and counterion has been realized. The kinetics of the formation o…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryTriad (anatomy)Inorganic Chemistrychemistry.chemical_compoundMonomermedicine.anatomical_structurechemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymermedicineProton NMREpichlorohydrinCounterionEthylene glycolMacromolecules
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