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showing 10 items of 2807 documents

From Bowls to Capsules: Assembly of Hexanuclear Ni II Rings Tailored by Alkali Cations

2020

An anionic hexanuclear NiII metallamacrocycle with endo and exo linking sites has been employed as a building block to generate a series of capsules and bowls of nanometric size. The supramolecular arrangement of the {Ni6 } rings was tailored by the size of the alkali cations, showing the transition from {Ni6 -M2 -Ni6 } capsules (M=LiI and NaI ) to {Ni6 -M} bowls (M=KI and CsI ). The alkyl co-cations are determinant to stabilize the assemblies by means of CH⋅⋅⋅π interactions on the exo side of the metallamacrocycles. The effect on the topology of the supramolecular assemblies of the cation size, cation charge, Et3 NH+ or Me4 N+ counter cations has been analyzed. Magnetic measurements reveal…

chemistry.chemical_classificationNíquelPropietats magnètiques010405 organic chemistryOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryBlock (periodic table)Alkali metal01 natural sciencesCatalysisAnàlisi de conglomerats0104 chemical sciencesCrystallographyNickelCluster analysischemistryNickelMagnetic propertiesAntiferromagnetismSelf-assemblyGround stateAlkylChemistry – A European Journal
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Group 4 and Group 8 unbridged metallocene derivatives with a pendant fluorenyl group. X-ray structure of 1,1′-bis[2-(2-fluorenyl)propyl]ferrocene

1999

Abstract The action of one equivalent of BuLi on 2-cyclopentadienyl-2-fluorenylpropane (C5H5CMe2C13H9) led to the monoanionic salt LiC5H4CMe2C13H9. This anion was reacted with Fe2Cl4(THF)3, TiCl3(THF)3, ZrCl4, HfCl4 or CpZrCl3, DME and, in a mixture with CpLi, with Fe2Cl4(THF)3 affording the corresponding metallocenes and metallocene dichlorides. The X-ray structure of Fe(η5-C5H4CMe2C13H9)2 is described. The first results about the reactivity of the fluorenyl group are reported together with the synthesis of Zr(η5-C5H5)[η5-C5H4CMe2-η5-C13H8Rh(cod)]Cl2, which has been tested using hydroformylation and cyclotrimerisation catalysis.

chemistry.chemical_classificationOrganic ChemistryX-raySalt (chemistry)BiochemistryMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundFerrocenechemistryGroup (periodic table)Materials ChemistryOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryMetalloceneHydroformylationJournal of Organometallic Chemistry
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Self-organization of substituted azacrowns based on their discoid and amphiphilic nature

1989

Abstract Cyclame and hexacyclene derivatives, bearing four and six long-chain substituents respectively, were synthesized. They are discussed as monolayer-forming amphiphiles as well as liquid-crystalline-phase-forming thermotropic mesogens. The compounds investigated form ordered monolayers at the gas/water interface. In the monolayer the hydrophilic cyclic head group lies flat on the water surface, whereas the hydrophobic substituents are oriented perpendicularly with respect to the interface. Most derivatives fitted with aromatic substituents exhibit a solid condensed state exclusively. In contrast with this, solid condensed as well as expanded phases can be found when spreading the alip…

chemistry.chemical_classificationPhase transitionMaterials scienceGeneral ChemistryCondensed Matter PhysicsThermotropic crystalCrystallographychemistryGroup (periodic table)Liquid crystalAmphiphileMonolayerOrganic chemistryGeneral Materials ScienceAlkylLiquid Crystals
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1992

chemistry.chemical_classificationPoly(methacrylic acid)Aqueous solutionSalt (chemistry)Block (periodic table)Chloridechemistry.chemical_compoundchemistryPhase (matter)Polymer chemistryCopolymermedicine1-methyl-4-vinylpyridiniummedicine.drugDie Makromolekulare Chemie, Rapid Communications
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Theoretical study of the OH addition to the endocyclic and exocyclic double bonds of the d-limonene

2005

Abstract The initial step of the d-limonene + OH gas-phase reaction mechanism was investigated by means of ab initio calculations. We have considered eight different possibilities for the OH addition, corresponding to the two C–C double bonds, the two C atoms of each double bond, and the syn or anti orientation, with respect to the isopropenyl group (endocyclic attack) or the ring cycle (exocyclic attack). Activation energies calculated at the QCISD(T)/6-31G(d)//UMP2/6-31G(d) level, show that there are preferred orientations for the OH addition under atmospheric conditions of temperature and pressure.

chemistry.chemical_classificationReaction mechanismCrystallographyTemperature and pressureD limoneneDouble bondchemistryStereochemistryGroup (periodic table)Ab initio quantum chemistry methodsGeneral Physics and AstronomyPhysical and Theoretical ChemistryRing (chemistry)Chemical Physics Letters
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Classification of vegetable oils according to their botanical origin using amino acid profiles established by High Performance Liquid Chromatography …

2010

Abstract A preliminary study using amino acid profiles to classify oils according to their botanical origin has been performed. Amino acid profiles were obtained from hydrolysis of proteins present in vegetable oils, and established by High Performance Liquid Chromatography (HPLC) with UV–vis detection. Proteins present in hazelnut, corn, soybean, olive, avocado, peanut and grapeseed oils were precipitated with acetone, and the residue was hydrolysed in acid medium. The amino acids obtained were derivatized with o -phthaldialdehyde and separated by HPLC. Peaks corresponding to 18 amino acids were observed using a C18 column and a gradient of acetonitrile–water in the presence of a 5 mM citr…

chemistry.chemical_classificationResidue (complex analysis)ChromatographyGeneral MedicineHigh-performance liquid chromatographyCitrate bufferAnalytical ChemistryAmino acidchemistry.chemical_compoundHydrolysisVegetable oilUltraviolet visible spectroscopychemistryAcetoneFood ScienceFood Chemistry
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Use of stable isotopes to investigate dispersal of waste from fish farm as a function of hydrodynamics.

2006

Stable isotopes were used to examine differential effects of fish farm waste on the water column and sediments. To achieve this objective, we chose 3 marine fish farms located along the coast of Sicily (Mediterranean Sea) as point-source disturbances, and a control area. The hypothesis that carbon and nitrogen isotope composition of particulate (POM) and sedimentary (SOM) organic matter varied with increasing distance (from cages to 1000 m) was tested at 3 levels of hydrodynam- ics: low (mean velocity of current (MVC) ~12 cm s -1 ), intermediate (MVC ~22 cm s -1 ), and high (MVC ~40 cm s -1 ). Different isotopic signals from allochthonous (fish waste) over natural (phytoplankton, terrigenou…

chemistry.chemical_classificationSettore BIO/07 - EcologiaEcologybusiness.industryTerrigenous sedimentStable isotope ratioFish farmingstable isotope aquaculture sedimentsAquatic ScienceIsotopes of nitrogenOceanographyWater columnMediterranean seachemistryAquacultureEnvironmental scienceOrganic matterFish farming Impact Water column Sediment Stable isotopes Hydrodynamics MediterraneanbusinessEcology Evolution Behavior and Systematics
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Role of peat organic matter on isotopic composition of most abundant benthic organisms in intertidal habitats of SW Iceland

2008

The transfer of peat organic matter (OM) from tidal pools of upper littoral to downstream rocky shores and its potential incorporation into marine biota were investigated using the stable isotope approach. Samplings were carried out in September 2004 in two SW Icelandic sites (Osar and Hvassahraun), where we selected (1) areas with shores where grass gently declined towards rocks and, on reaching the sea line, formed small tidal peat pools and (2) areas where grass and rocky shores were not contiguous, rather the grass lower limits were several hundreds of meters back from the shore. In both grass and no grass areas, in the intertidal zone, all benthic organisms and all potential OM sources…

chemistry.chemical_classificationSettore BIO/07 - EcologiaPeatEcologyEcologyIntertidal zoneFucus vesiculosusBiotaAquatic ScienceBiologybiology.organism_classificationRocky shoreOceanographyBenthic organism · Intertidal environment · Grass-pool · Peat · Stable isotope · Iceland · North AtlanticchemistryBenthic zoneLittoral zoneOrganic matterEcology Evolution Behavior and Systematics
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Sources of organic matter for inter-tidal consumers in Ascophyllum-shores (Sw Iceland): a multi stable isotope approach.

2007

Stable isotopes were used to examine the origin of organic matter in Icelandic Ascophyllum-based habitats, the role of different organic matters in filling intertidal food webs and the food preferences of the most abundant suspension feeders, grazers and predators. We selected three intertidal sites on the SW coast of Iceland where we sampled in early September 2004, organic matter sources (POM, SOM and most abundant primary producers, A. nodosum and F. vesciculosus) and the most abundant macrofauna species (barnacles, mussels, gastropods, sponge and crabs). Even though the primary production (Ascophyllum-based) was the same at the three study sites, the isotopic composition of common-among…

chemistry.chemical_classificationSettore BIO/07 - EcologiaPrimary producersbiologyEcologyStable isotope ratioIntertidal zoneAquatic ScienceIntertidal ecologyOceanographybiology.organism_classificationFood webchemistryHabitatBenthic organism Intertidal environment Stable isotope Iceland North AtlanticEnvironmental scienceOrganic matterAscophyllum
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Remarkably Robust Group 4 Metal Half-Sandwich Complexes Containing Two Higher Alkyl Ligands:  X-ray Structure and Reactivity of the Di-n-butyl Comple…

1997

The reaction of LiR with M(η5:η1:η1-C5Me4SiMe2NCH2CH2OMe)Cl2 (1, M = Zr (a), Hf (b)) gives the isolable, thermally stable complexes M(η5:η1:η1-C5Me4SiMe2NCH2CH2OMe)R2 (R = Et (2), nPr (3), nBu(4)), which contain two alkyl ligands with β-hydrogen atoms.

chemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryX-rayInorganic ChemistryMetalCrystallographyGroup (periodic table)visual_artvisual_art.visual_art_mediumReactivity (chemistry)Physical and Theoretical ChemistryAlkylOrganometallics
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