Search results for "functional group"

showing 10 items of 61 documents

Equilibrium/steady-state concept in phytoplankton ecology

2003

This paper summarises the outcomes of the 13th Workshop of the International Association of Phytoplankton Taxonomy and Ecology (IAP). The authors mostly addressed their contributions on the following topics: the effect of trophic state on the attainment of a steady-state; the establishment of equilibria in deep and shallow lakes; the role of spatial heterogeneity, disturbance, and stress in the establishment of equilibrium assemblages; the mechanisms leading to the steady state; the frequency and longevity of equilibrium phases, and the role of morphological and physiological plasticity of phytoplankton in maintaining the (apparently) same populations under different environmental condition…

Settore BIO/03 - Botanica Ambientale E ApplicataAquatic Scienceequilibrium steady-state functional groups phytoplankton associationsHydrobiologia
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Comparing biological classifications of freshwater phytoplankton: a case study from South China

2012

The use of ecological classification systems is becoming more and more widely used when studying phytoplankton. Grouping phytoplankton species into ecologically coherent groups allow to reduce redundancy and in this way, to handle a minor number of biological variables when investigating the ecological status of aquatic ecosystems. Three ecological classifications are mostly used when freshwater phytoplankton is studied: functional groups or coda, morpho-functional groups (MFGs) and morphology-based functional groups (MBFGs). In this study, these three ecological classifications were comparatively used along with two taxonomic classifications based on species and genera to analyse phytoplan…

South chinaEcologyCanonical correspondence analysisAquatic ecosystemEcology (disciplines)Settore BIO/03 - Botanica Ambientale E ApplicataPhytoplanktonFunctional groups Morpho-functional groups Morphology-based functional groups Taxonomic groups Physical constraints ReservoirsTaxonomic rankAquatic ScienceBiologyExplained variationCodaHydrobiologia
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Synthesis of a Linear Assembly Consisting of a Central Ru(Phen)32+ Derivative and Two Peripheral Porphyrins

2002

A ruthenium(II) precursor complex containing a bis-phenanthroline ligand, leading to a controlled helical structure around the metal centre, and a third phenanthroline-type ligand has been prepared. The spatial arrangement of the system is such that two chemical groups are disposed trans to one another on an axis running through the Ru centre. By appropriate functional group transformation, these two groups can be attached to monosubstituted zinc(II) porphyrins (PZn) to afford a linear array consisting of a central ruthenium(II) complex and two peripheral PZn motifs. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

StereochemistryLigandOrganic Chemistrychemistry.chemical_elementZincLinear arrayRutheniumMetalchemistry.chemical_compoundCrystallographychemistryvisual_artFunctional groupChemical groupsvisual_art.visual_art_mediumPhysical and Theoretical ChemistryDerivative (chemistry)European Journal of Organic Chemistry
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The mechanism of hydrolysis of beta-glycerophosphate by kidney alkaline phosphatase.

1975

1. To identify the functional groups that are involved in the conversion of β-glycerophosphate by alkaline phosphatase (EC 3.1.3.1) from pig kidney, the kinetics of alkaline phosphatase were investigated in the pH range 6.6-10.3 at substrate concentrations of 3 μM-30 mM. From the plots of log ṼH+ against pH and log ṼH+/KH+m against pH one functional group with pK = 7.0 and two functional groups with pK = 9.1 were identified. These groups are involved in substrate binding. Another group with pK = 8.8 was found, which in its unprotonated form catalyses substrate conversion. 2. GSH inhibits the alkaline phosphatase reversibly and non-competitively by attacking the bound Zn(II). 3. The influenc…

StereochemistrySwineKidneyBiochemistrychemistry.chemical_compoundHydrolysisAnimalsMagnesiumBinding siteMolecular Biologychemistry.chemical_classificationBinding SitesHydrolysisSubstrate (chemistry)Cell BiologyGlutathioneHydrogen-Ion ConcentrationPhosphateAlkaline PhosphataseGlutathioneKineticsZincEnzymechemistryModels ChemicalGlycerophosphatesFunctional groupAlkaline phosphataseResearch ArticleThe Biochemical journal
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Two dimensional self-assembly of bis-acylureas having various functional end groups.

2011

We present the synthesis and morphology study of thirteen bis-acylurea molecules with various functional end groups. The bis-acylureas have two acylurea groups, -NH-CO-NH-CO-, divided by a pentamethylene spacer, -(CH(2))(5)-, and two symmetric functional end groups, such as, aliphatic, benzyl, mono- and bi-thiophenyl, sulfur-containing, and propargyl (HC[triple bond]CCH(2)-) moieties. The bis-acylureas were synthesized by the coupling reactions of ureas with pimeloyl chloride or pimelic acid. Upon cooling from hot isotropic solutions, the bis-acylureas spontaneously form supermolecules. In the cases of aliphatic, benzyl, mono- and bi-thiophenyl functional groups, two dimensional supramolecu…

Steric effectsModels MolecularStereochemistrySupramolecular chemistryHydrogen BondingCrystal structureSupermoleculeCrystallography X-RaySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundCrystallographyEnd-groupColloid and Surface ChemistrychemistryPropargylFunctional groupMoleculeUreaJournal of colloid and interface science
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Molecular surface calculations on organic compounds

1992

Abstract The molecular surface area was calculated for 82 hydrocarbons, esters, ethers, alcohols and ketones including linear, branched and cyclic ones. The relationship between the aqueous solubility and the molecular surface area was determined for each family of compounds and for all the families together. The results show that solubility is mainly determined by molecular surface area and that the influence of functional group is the same for all the oxygen containing compounds studied.

Surface (mathematics)chemistry.chemical_compoundAqueous solutionChemistryAqueous solubilityFunctional groupOrganic chemistrychemistry.chemical_elementPhysical and Theoretical ChemistrySolubilityCondensed Matter PhysicsBiochemistryOxygenJournal of Molecular Structure: THEOCHEM
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Rapid and eco-friendly synthesis of graphene oxide-silica nanohybrids

2014

The increasing interest in Graphene oxide (GO) is due to many issues: the presence of both sp2-conjugated atoms and oxygen-containing functional groups provides a strong hydrophilicity and the possibility to further functionalize it with other molecules (i.e. π-π interactions covalent attachment etc.) [1]. Furthermore since the GO is biocompatible and noncytotoxic many studies have been recently focused on the development of GO-based nanodevices for bioimaging DNA detection drug delivery. Due to their low cytotoxicity and large internal surface area silica nanoparticles have been taken into account as promising material for biolabeling and drug loading/delivery. Particular consideration has recently been demonstrated for GO-silica composites because of the potentialities for electrical applications their chemical inertia and stability toward ions exposure. The possibility to combine the extraordinary properties of GO and silica offers several advantages for the realization of nanoprobes for biological applications and of biosensor [12]. The strategy for the fabrication of GO-nanosilica nanohybrids can be schematized as follows: (i) synthesis of GO by oxidizing graphite powder with the method described by Marcano et al. [3] (ii) Preparation of oxygen-loaded silica nanoparticles by thermal treatments in controlled atmosphere in order to induce high NIR emission at 1272 nm from high purity silica nanoparticles. (iii) preparation of GrO-silica nanohybrid films via rapid solvent casting in water. The nanohybrids were tested by XPS FTIR Raman analysis UV photoluminescence analysis TGA Zeta potential measurements electrical tests AFM and SEM. Several nanohybrids were prepared by combining two different typologies of GO and two different samples of silica.
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Molecular analyses of soil denitrifying bacteria

2006

[SDV] Life Sciences [q-bio][SDE] Environmental Sciences[SDV]Life Sciences [q-bio][SDE]Environmental SciencesFUNCTIONAL GROUP LEVELSPLANT MICROORGANISMSMOLECULAR METHODS
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Efficient synthesis of new C-functionalized macrocyclic polyamines

2010

A powerful synthetic route for the preparation of new poly-azamacrocycles, valuable precursors of bifunctional chelating agents with applications in nuclear medicine, is reported. The desired functional group was introduced onto the macro-cycle backbone during the cyclization step, thus avoiding the tedious preparation of a C-functionalized synthon. The regioselective reaction of macrocycles bearing an aminomethyl pendant arm with aldehydes is also described.

amines010402 general chemistry01 natural sciencesAldehydeChemical synthesischemistry.chemical_compoundN ligands[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistryChelationPhysical and Theoretical ChemistryBifunctionalComputingMilieux_MISCELLANEOUSchemistry.chemical_classification010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistrySynthonRegioselectivity0104 chemical sciences3. Good healthmacrocycleschemistryFunctional groupbifunctional chelating agents
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Palladium-catalyzed heteroaryl thioethers synthesis overcoming palladium dithiolate resting states inertness: Practical road to sulfones and NH-sulfo…

2018

International audience; We provide efficient synthetic access to heteroaryl sulfones in two-steps using a simple palladium-1,1'-bis [(diphenyl)phosphanyl]ferrocene catalyst to form in high yields variously functionalized heteroaromatic thioethers. Pyridinyl-containing substrates can be subsequently selectively oxidized into sulfones and NH-sulfoximines by using very mild oxidation conditions with a high functional group tolerance. In the palladium catalyzed C-S coupling of heteroaromatic thiols, reactivity limitation is attached with electron-deficient thiols. We show that this limitation can be resolved by the successful use of 2-bromoheteroarenes in the C-S coupling. We established herein…

bond formationarenessulfideschemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisefficientCatalysischemistry.chemical_compounds-arylation[CHIM]Chemical SciencesReactivity (chemistry)SulfonesResting statethiols[PHYS]Physics [physics]010405 organic chemistryProcess Chemistry and TechnologyGeneral Chemistryindolesacid saltsCombinatorial chemistry0104 chemical sciencesThiolatesC-S couplingchemistryFerroceneNH-sulfoximinesReagentElectrophileFunctional groupH functionalizationdirecting groupPalladiumStoichiometryPalladiumCatalysis Communications
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