Search results for "functional group"

showing 10 items of 61 documents

Pyrene derived functionalized low molecular weight organic gelators and gels

2008

Pyrene derived binary functionalized low molecular weight organic gelators (FLMOGs) and gels thereof in selected organic solvents were synthesized and characterized. The functionality refers to a functional group that does not take part in formation of the supramolecular gel network, but remains free and available for other purposes, such as to bind nanoparticles or other molecules into the gel structure. Functional groups were observed to disturb gel formation strongly, if they interact with each other within the same supramolecule due to the formation of competitive structures. Preventing such interactions restored the original gel properties. A gel with weaker supramolecular bonding than…

Binding energySupramolecular chemistryGeneral ChemistryCatalysisFluorescence spectroscopySolventchemistry.chemical_compoundsymbols.namesakechemistryFunctional groupPolymer chemistryMaterials ChemistrysymbolsMoleculePyrenevan der Waals forceNew Journal of Chemistry
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Drug Screening Boosted by Hyperpolarized Long-Lived States in NMR

2014

International audience; : Transverse and longitudinal relaxation times (T1ρ and T1 ) have been widely exploited in NMR to probe the binding of ligands and putative drugs to target proteins. We have shown recently that long-lived states (LLS) can be more sensitive to ligand binding. LLS can be excited if the ligand comprises at least two coupled spins. Herein we broaden the scope of ligand screening by LLS to arbitrary ligands by covalent attachment of a functional group, which comprises a pair of coupled protons that are isolated from neighboring magnetic nuclei. The resulting functionalized ligands have longitudinal relaxation times T1 ((1) H) that are sufficiently long to allow the powerf…

BromidesMagnetic Resonance SpectroscopyStereochemistryDrug Evaluation PreclinicalThiophenesLigands010402 general chemistry01 natural sciencesBiochemistrydynamic nuclear polarizationchemistry.chemical_compoundNMR spectroscopyCatalytic DomainDrug DiscoveryGeneral Pharmacology Toxicology and PharmaceuticsPharmacologySpins[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryDrug discoveryOrganic ChemistryRelaxation (NMR)ProteinsNuclear magnetic resonance spectroscopyFull PapersLigand (biochemistry)0104 chemical sciencesCrystallographychemistryCovalent bondlong-lived statesExcited stateFunctional groupMolecular MedicineChemMedChem
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Gas—liquid chromatographic analyses

1984

Abstract The gas chromatography (GC) of n -alkyl acetates (CH 3 COOR), chloroacetates (CH 2 ClCOOR), dichloroacetates (CHCl 2 COOR) and trichloroacetates (CCl 3 COOR), where the alcohol chain length (R) varied between 1 and 8, and certain of their monochlorinated derivatives, 176 compounds altogether, has been studied on SE-30 and OV-351 glass capillary columns under the same operating conditions. The isomeric monochlorinated esters are eluted in direct order from the 1- chloro to the ω-chloro isomer, the separation of the isomers being complete on OV- 351. On SE-30, however, the peaks of the 6- and 7-chlorooctyl esters are partly overlapped. The separation of the mixtures of odd- and e…

Capillary actionAnalytical chemistryAlcoholFormyl groupAldehydeBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary columnStraight chainpolycyclic compoundsStructural isomerOrganic chemistryMethyleneBenzoic acidchemistry.chemical_classificationPrimary (chemistry)General MedicineCapillary gas chromatographyBoiling pointChromatographic separationSalicylaldehydeNitrobenzoatesPolarlipids (amino acids peptides and proteins)Aliphatic compoundResolution (mass spectrometry)Polarity (physics)Carboxylic acidchemistry.chemical_elementBranching (polymer chemistry)Isothermal processTurn (biochemistry)ChlorinePhenolsQuartzAlkylTetradecaneChlorophenolDegree of unsaturationChromatographyGeminalElutionOrganic ChemistryChloroacetatesComplete resolutionReverse orderChain lengthchemistryChlorobenzeneFunctional groupNitroKovats retention indexNon polarGas chromatographyVicinalGas liquid chromatographicJournal of Chromatography A
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Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Aryl Chlorobenzoates with Alkyl Grignard Reagents

2020

Aryl benzoates are compounds of high importance in organic synthesis. Herein, we report the iron-catalyzed C(sp2)&ndash

Chlorobenzoatesaryl estersPharmaceutical ScienceMedicinal chemistryArticleCatalysisAnalytical ChemistryCatalysislcsh:QD241-441chemistry.chemical_compoundironlcsh:Organic chemistryDrug Discoverycross-couplingPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationNucleophilic additionMolecular StructureArylOrganic ChemistryBenzoatesChlorobenzoateschemistryChemistry (miscellaneous)Fe-catalysisFunctional groupKumada cross-couplingMolecular MedicineOrganic synthesisC–O activationIron CompoundsMolecules
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Formation of a novel ferromagnetic end-to-end cyanate bridged homochiral helical copper(ii) Schiff base complex via spontaneous symmetry breaking

2014

A homochiral helical coordination polymer of copper(II) has been synthesized using achiral precursors via spontaneous symmetry breaking and has been confirmed by single crystal X-ray diffraction and solid-state CD spectroscopy. The variable temperature magnetic measurements indicate the presence of weak ferromagnetic exchange interactions mediated by end-to-end cyanate bridges (J = +0.12 cm(-1)).

Circular dichroismSchiff baseStereochemistryChemistryCoordination polymerSpontaneous symmetry breakingchemistry.chemical_elementcircular dichroism spectroscopyCyanateferromagnetismsingle crystalsCopperX-ray diffractionInorganic ChemistryCrystallographychemistry.chemical_compoundfunctional groupsFerromagnetismcopperferromagnetic materialsta116Single crystalDalton Transactions
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Towards a functional classification of the freshwater phytoplankton

2002

This paper considers the structure of freshwater phytoplankton assemblages and promotes a scheme of ‘vegetation recognition’, based upon the functional associations of species represented in the plankton. These groups are often polyphyletic, recognizing commonly shared adaptive features, rather than common phylogeny, to be the key ecological driver. Thirty-one such associations are outlined and the basic pattern of their distinctive ecologies is outlined. An invitation to other plankton scientists to assist in the development of this scheme is issued.

EcologyEcologyPolyphylyfungiPhytoplanktonSettore BIO/03 - Botanica Ambientale E ApplicataAquatic SciencePlanktonBiologyPhytoplankton Functional Groups Biological ClassificationEcology Evolution Behavior and Systematics
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Shifts in macroalgal communities in relation to some abiotic factors: a functional group approach

2007

The aim of the present study was to test whether the functional group approach is effective in describing changes in community structure, resulting from exposure to different substratum inclination and levels of organic pollution. The results of this study suggest that the functional group approach could detect changes in community structure as response to some abiotic factors. However, since species response is not always a functional group response, this method is difficult to generalize and a better definition of the functional group model is required.

Functional groups community structure abiotic factors
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Calcium binding and ionic conduction in single conical nanopores with polyacid chains: model and experiments.

2012

Calcium binding to fixed charge groups confined over nanoscale regions is relevant to ion equilibrium and transport in the ionic channels of the cell membranes and artificial nanopores. We present an experimental and theoretical description of the dissociation equilibrium and transport in a single conical nanopore functionalized with pH-sensitive carboxylic acid groups and phosphonic acid chains. Different phenomena are simultaneously present in this basic problem of physical and biophysical chemistry: (i) the divalent nature of the phosphonic acid groups fixed to the pore walls and the influence of the pH and calcium on the reversible dissociation equilibrium of these groups; (ii) the asym…

General Physics and AstronomyIonic bondingFunctionalizedDissociation (chemistry)Conical nanoporeNanoscale regionschemistry.chemical_compoundNanoporesI - V curveIonic conductivityGeneral Materials ScienceConical nanoporesPhosphonate groupCalcium concentrationChemistryGeneral EngineeringPH effectsPartition functionsIonic channelsIon equilibriumReversible dissociationChemical physicsFunctional groupsThermodynamicsDesalination membranesIon bindingPorosityDissociationBiophysical chemistryDissociation equilibriaInorganic chemistrychemistry.chemical_elementWater filtrationCalciumIonNernst-Planck equationsApplied potentialsIon bindingCarboxylationPhosphonic acidsComputer SimulationCarboxylateParticle SizeControlled drug releaseCurrent voltage curveIonsBinding SitesFixed charge densityPH sensitiveCarboxylic acidsDesalinationPhosphonic acid groupsPoly acidsElectric ConductivityCarboxylic acid groupsFixed ChargesNanostructuresCell membranesCurrent-voltage curvesModels ChemicalQuantum theoryFISICA APLICADACalciumBiological ion channelsCalcium bindingIonic currentCytologyPore wallStatistical mechanicsAcidsACS nano
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Use and misuse in the application of the phytoplankton functional classification: a critical review with updates

2008

Since its publication, the article ‘Towards a functional classification of the freshwater phytoplankton’ (Reynolds et al., J Plankton Res 24: 417–428, 2002), has attracted the attention of dozens of phytoplankton ecologists worldwide. These numerous applications of the functional classification to describe phytoplankton patterns in various aquatic ecosystems allowed the recognition of some uncertain features of this concept originating from various reasons. In this article, we attempt to facilitate the application of the functional classification, by providing a detailed description of the typical misplacements and by modifying some of the original habitat templates and species allocations.…

GeographyWater Framework DirectiveHabitatEcologyAquatic ecosystemEcology (disciplines)PhytoplanktonAquatic SciencePlanktonFunctional groups Codon Phytoplankton Water Framework DirectiveFunctional group (ecology)Hydrobiology
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The effect of tether groups on the spin states of iron(ii)/bis[2,6-di(pyrazol-1-yl)pyridine] complexes

2021

The synthesis of six 2,6-di(pyrazol-1-yl)pyridine derivatives bearing dithiolane or carboxylic acid tether groups is described: [2,6-di(pyrazol-1-yl)pyrid-4-yl]methyl (R)-lipoate (L1), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]ethyl (R)-lipoate (L2), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxy]ethyl (R)-lipoate (L3), N-([2,6-di(pyrazol-1-yl)pyrid-4-ylsulfanyl]-2-aminoethyl (R)-lipoamide (L4), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]acetic acid (L5) and 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]propionic acid (L6). The iron(ii) perchlorate complexes of all the new ligands exhibit gradual thermal spin-crossover (SCO) in the solid state above room temperature, except L4 who…

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundAcetic acidPerchloratechemistrySpin statesCarboxylic acidPyridineFunctional groupRing (chemistry)Medicinal chemistryDithiolaneDalton Transactions
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