Search results for "Spectroscopy"

showing 10 items of 10293 documents

Pyrrolide-imine benzyl complexes of zirconium and hafnium: synthesis, structures, and efficient ethylene polymerization catalysis

2004

Abstract A series of pyrrolyl-imines HL1–6 was prepared by the condensation of pyrrole-2-carboxyaldehyde with different amines. The reaction of 2 equiv of pyrrolyl-imine with tetrabenzyl complexes of hafnium and zirconium M(CH2Ph)4 (M=Hf or Zr) gave dibenzyl complexes (L3–6)2M(CH2Ph)2, which were characterized by NMR spectroscopy and crystal structure analysis. NMR spectra of the complexes with secondary alkyl substituents at the imine nitrogen (isopropyl: 3a, 4-tert-butylcyclohexyl: 4a and 4b) suggest that rapid racemization between Δ and Λ configurations occurs in solution on the NMR time scale. The complexes with pyrrolide-imine ligands with a tertiary alkyl group such as tert-butyl (5a …

chemistry.chemical_classificationZirconiumOrganic ChemistryImineCationic polymerizationMethylaluminoxanechemistry.chemical_elementNuclear magnetic resonance spectroscopyBiochemistryInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryRacemizationIsopropylAlkylJournal of Organometallic Chemistry
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Functionalization of Bambusurils by a Thiol-Ene Click Reaction and a Facile Method for the Preparation of Anion-Free Bambus[6]urils

2018

Sulfide-functionalized bambus[4]urils ((RS)8 BU[4]) and bambus[6]urils ((RS)12 BU[6]) were synthesized through thiol-ene click coupling reactions (TEC) of allylbambus[n]urils. Thiosugars were grafted to BU[4] and BU[6]. Synthesis of BU[6] derivatives always requires the use of a template anion (iodide, chloride, or bromide), which is enclosed in the cavity of BU[6]. We show that this anion influences the reactivity of bambus[6]urils. An encapsulated iodide makes allyl functions of allyl12 BU[6] less reactive towards TEC and hydrogenation reactions in comparison to the corresponding chloride or bromide inclusion complexes. This is critical for the chemical reactivity of BU[6] and even more t…

chemistry.chemical_classification[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic ChemistryIodideGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesMedicinal chemistryQuantum chemistryCatalysisCoupling reaction0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistryBromide[CHIM.CRIS]Chemical Sciences/CristallographyClick chemistryReactivity (chemistry)Ene reactionChemistry - A European Journal
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Sorting of Enhanced Reference Raman Spectra of a Single Amino Acid Molecule

2014

In this contribution, we report the identification of the principal reference Raman spectra of a single cystein molecule. To that purpose, we design an active Surface Enhanced Raman Spectroscopy (SERS) template based on surfactant-less Chebyshev nanoparticles operating in a microfluidic platform. A principal component analysis is obtained from fluctuating spectra to sort the reference spectra of cystein. The assignment of Raman bands brings new insight into the conformation of an amino acid adsorbed onto gold nanoparticle.

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Quantitative Biology::BiomoleculesSortingNanoparticleActive surfaceQuantitative Biology::GenomicsSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidCrystallographysymbols.namesakeGeneral EnergyAdsorptionchemistrysymbolsMoleculePhysical and Theoretical ChemistryRaman spectroscopyComputingMilieux_MISCELLANEOUSThe Journal of Physical Chemistry C
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Concentration of amino acids using supported liquid membranes with di-2-ethylhexyl phosphoric acid as a carrier

1997

Abstract Basic studies of a procedure for extraction of amino acids using a supported liquid membrane containing di-2-ethylhexyl phosphoric acid are presented. The extractions are made from an aqueous donor phase with pH 3 to a more acidic acceptor phase and the mass transfer is driven by the proton gradient between these phases. For 0.01 mM tryptophan and with 1 M HCl as acceptor phase, an extraction efficiency of 60% is obtained, constant up to at least 12 h. This permits concentration enrichment factors linearly increasing with time up to values of at least 150. For higher amino acid concentrations, the extraction efficiency is constant only over shorter time intervals.

chemistry.chemical_classificationamino acidsphosphonic acidAqueous solutionChromatographyDEHPAChemistryExtraction (chemistry)TryptophanDi-(2-ethylhexyl)phosphoric acidBiochemistryAcceptorAnalytical ChemistryAmino acidchemistry.chemical_compoundMembranesupported liquid membrane extractiondi-2-ethylhexylEnvironmental ChemistryPhosphoric acidSpectroscopyAnalytica Chimica Acta
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Cycloartane Glycosides from Three Species of Astragalus (Fabaceae)

2011

Nine cycloartane-type glycosides were isolated from three species of the genus Astragalus (Fabaceae): From the aerial parts of A. cicer L., two new saponins, cicerosides A and B (1 and 2, resp.), i.e., a tetradesmosidic and tridesmosidic cycloartane-type glycosides besides one known compound, from the roots of A. sempervirensLam., one known saponin, and from the roots of A. ptilodesBoiss. var. cariensisBoiss., five known compounds. Their structures were established mainly by 600-MHz 2D-NMR techniques (1H,1H-COSY, TOCSY, NOESY, HSQC, and HMBC) and mass spectroscopy.

chemistry.chemical_classificationbiologyAstragalus speciesOrganic ChemistrySaponinGlycosideFabaceaebiology.organism_classificationBiochemistryCatalysisInorganic ChemistryAstragaluschemistryGenusDrug DiscoveryBotanyPhysical and Theoretical ChemistryTwo-dimensional nuclear magnetic resonance spectroscopyHelvetica Chimica Acta
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Alkyl and diether bridged N,N,N′,N′-tetra(2-hydroxybenzyl)diamines: effects of hydrogen bonding on structure and solubility

2012

A solvent-free one-step method has been used to prepare two N,N,N′,N′-tetra(2-hydroxy-3,5-dimethylbenzyl)diaminoalkanes containing a long n-alkyl bridge (6 and 8 CH2 groups between N-atoms). In addition, three novel N,N,N′,N′-tetra(2-hydroxy-5-alkyl-3-alkylbenzyl)-diaminoalkane-ethers (alkyl = methyl or t-butyl) have been prepared using the same method. The compounds were studied in the solid state using single crystal X-ray diffraction and their solubility was studied using UV/Vis spectroscopy. In the solid state, hydrogen bonding plays a key role in controlling the crystal packing and conformations of the molecules, thus affecting the solubility and properties of the compounds.

chemistry.chemical_classificationbiologyChemistryHydrogen bondGeneral ChemistryCondensed Matter Physicsbiology.organism_classificationMedicinal chemistryCrystalOrganic chemistryMoleculeTetralipids (amino acids peptides and proteins)General Materials ScienceSolubilitySpectroscopyta116Single crystalAlkylCrystEngComm
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Self-Assembled Polymers Based on bis-Tetra-Urea Calix[4]arenes Connected via the Wide Rim

2008

Six double calixarenes were synthesised in which two tetra-urea calix[4]arenes are linked by a rigid spacer between the urea functions at their wide rim. The dimerisation of their tetra-urea parts leads to hydrogen-bonded polymeric assemblies in apolar solvents. The addition of the stoichiometric amount of a tetra-tosylurea calix[4]arene disrupts the polymeric structures due to the preferred formation of heterodimeric capsules between tetra-aryl and tetra-tosylurea calix[4]arenes. The existence of polymeric assemblies was further established by AFM studies on spin-coated samples.

chemistry.chemical_classificationbiologyChemistryHydrogen bondGeneral ChemistryPolymerNuclear magnetic resonance spectroscopybiology.organism_classificationchemistry.chemical_compoundPolymer chemistryCalixareneUreaTetraOrganic chemistrySelf-assemblyStoichiometrySupramolecular Chemistry
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Foetidissimosides C–F, Novel Glycosides from the Roots ofCucurbita foetidissima

2004

Two novel echinocystic acid (=(3β,16α)-3,16-dihydroxyolean-12-en-28-oic acid) glycosides, foetidissimosides C (1), and D (2), along with new cucurbitane glycosides, i.e., foetidissimosides E/F (3/4) as an 1 : 1 mixture of the (24R)/(24S) epimers, were obtained from the roots of Cucurbita foetidissima. Their structures were elucidated by means of a combination of homo- and heteronuclear 2D-NMR techniques (COSY, TOCSY, NOESY, ROESY, HSQC, and HMBC), and by FAB-MS. The new compounds were characterized as (3β,16α)-28-{[O-β-D-glucopyranosyl-(13)-O-β-D-xylopyranosyl-(14)-O-6-deoxy-α-L-mannopyranosyl-(12)-α-L-arabinopyranosyl]oxy}-16-hydroxy-28-oxoolean -12-en-3-yl β-D-glucopyranosiduronic acid (1…

chemistry.chemical_classificationbiologyChemistryStereochemistryOrganic ChemistryGlycosideCucurbitanebiology.organism_classificationBiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundHeteronuclear moleculeDrug DiscoveryEpimerCucurbita foetidissimaPhysical and Theoretical ChemistryEchinocystic acidTwo-dimensional nuclear magnetic resonance spectroscopyHeteronuclear single quantum coherence spectroscopyHelvetica Chimica Acta
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Bafouoside C, a new triterpenoid saponin from the roots of Cussonia bancoensis Aubrev. & Pellegr.

2014

Abstract A new triterpenoid saponin named bafouoside C 3-O-β- d -glucopyranosyl-(1 → 4)-[β- d -galactopyranosyl-(1 → 2)]-β- d -glucuronopyranosyloleanolic acid 28-O-β- d -glucopyranosyl ester; (1), together with five known compounds 3-O-β- d -galactopyranosyl-(1 → 2)-β- d -glucuronopyranosyloleanolic acid (2), 23-hydroxyursolic acid (3), 28-O-α- l -rhamnopyranosyl-(1 → 4)-O-β- d -glucopyranosyl-(1 → 6)-O-β- d -glucopyranosyl-23-hydroxyursolic acid (4), 3-O-β- d -glucopyranosyl-23-hydroxyursolic acid (5), and 3-O-α- l -arabinopyranosyl-23-hydroxyursolic acid (6), were isolated from the roots of Cussonia bancoensis Aubrev. & Pellegr. Their structures were established on the basis of 1D- and 2…

chemistry.chemical_classificationbiologyCussoniaStereochemistryPlant Sciencebiology.organism_classificationBiochemistryNmr datachemistryCarcinoma CellAraliaceaeAgronomy and Crop ScienceHuman breastTwo-dimensional nuclear magnetic resonance spectroscopyHuman colonBiotechnologyTriterpenoid saponin
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Spirostane and cholestane glycosides from the bulbs of Allium nigrum L

2011

Abstract A phytochemical investigation of the fresh bulbs of Allium nigrum L. led to the isolation of new spirostane-type glycosides as two inseparable isomer mixtures, nigrosides A1/A2 (1a/1b) and nigrosides B1/B2 (2a/2b), two new cholestane-type glycosides, nigrosides C and D (3 and 4), together with the known compounds, 25(R,S)-5α-spirostan-2α,3β,6β-trio1-3-O-β- d -glucopyranosyl-(1 → 2)-O-[β- d -xylopyranosyl-(1 → 3)]-O-β- d -glucopyranosyl-(1 → 4)-β- d -galactopyranoside (5a/5b) and 25(R,S)-5α-spirostan-2α,3β,6β-trio1 3-O-β- d -glucopyranosyl-(1 → 2)-O-[4-O-(3S)-3-hydroxy-3-methylglutaryl-β- d -xylopyranosyl-(1 → 3)]-O-β- d -glucopyranosyl-(1 → 4)-β- d -galactopyranoside (6a/6b), isola…

chemistry.chemical_classificationbiologyLiliaceaeStereochemistrySaponinGlycosideGeneral Medicinebiology.organism_classificationAllium nigrumAnalytical Chemistrychemistry.chemical_compoundchemistryPhytochemicalAlliumCholestaneTwo-dimensional nuclear magnetic resonance spectroscopyFood ScienceFood Chemistry
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