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showing 10 items of 2807 documents

Ancillary Ligand Effect on Single-Site Styrene Polymerization:  Isospecificity of Group 4 Metal Bis(phenolate) Catalysts

2003

Styrene is polymerized isospecifically by group 4 metal complexes that contain a C2-symmetrically coordinated 1,4-dithiabutane-linked bis(phenolato) ligand activated by methylaluminoxane.

ChemistryLigandMethylaluminoxaneGeneral ChemistryBiochemistryCatalysisStyreneCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryPolymerizationSingle siteGroup (periodic table)visual_artPolymer chemistryvisual_art.visual_art_mediumJournal of the American Chemical Society
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Myrosinase activity and quality parameters on fresh-cut Chinese cabbage stored at two different temperatures

2009

ChemistryMyrosinaseMyrosinase activityBioengineeringSettore AGR/15 - Scienze E Tecnologie AlimentariGeneral MedicineFood scienceenzymes vegetables ready-to-eat storageMolecular BiologyBiotechnologyNew Biotechnology
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Über gemischte Gruppe 14—Gruppe 14-Bindungen

1991

Abstract p-Tol6PbSn has been synthesized by reaction of p-Tol3PbLi with p-Tol3SnI in THF/ether (1:2) at −78°C. The crystal structures of p-Tol4Pb (I 4 ) and of p-Tol6Sn2, p-Tol6PbSn and p-Tol6Pb2 have been determined. The three dinuclear compounds crystallize not strickly isomorphous. They exhibit the same space group (R 3 and rather similar unit cell dimensions. Yet according to the solvent of crystallization, two types with differing atomic position parameters can be distinguished (“homoeotypism with differences of parameters” in the definition of Laves). In both types, the individual molecules have a chiral C3-symmetric conformation and the non-chiral unit cell encloses both enantiomers.…

ChemistryOrganic ChemistryEtherCrystal structureBiochemistrylaw.inventionInorganic ChemistrySolventchemistry.chemical_compoundCrystallographysymbols.namesakeGroup (periodic table)lawMaterials ChemistrysymbolsMoleculePhysical and Theoretical ChemistryEnantiomerCrystallizationRaman spectroscopyJournal of Organometallic Chemistry
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The Zwitterion [8,8′-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3′-Co]0 as a Versatile Building Block To Introduce Cobalt Bis(Dicarbollide) Ion into Organic Molecu…

2012

The synthesis of a new bridged [8,8′-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3′-Co]0 derivative (2), arising from the acid-catalyzed reaction of cobalt bis(1,2-dicarbollide)(1−) ion with formaldehyde, is reported. The proposed reaction path is supported by the isolation of side products including two zwitterionic compounds, the known bridged [8,8′-μ-(CH3O)-(1,2-C2B9H10)2-3,3′-Co]0 derivative (3), the new zwitterion [(8-(CH3)2O-1,2-C2B9H10)-(1′,2′-C2B9H11)-3,3′-Co]0 (4), and two anionic compounds—the known [(8,8′-Cl2-1,2-C2B9H10)2-3,3′-Co]− and the newly characterized dimethoxy derivative [(8,8′-(CH3O)2-1,2-C2B9H10)2-3,3′-Co]− of the cobalt bis(dicarbollide) ion. Compound 2 serves as a versatile buildi…

ChemistryOrganic ChemistryFormaldehydechemistry.chemical_elementBlock (periodic table)Organic moleculesIonInorganic Chemistrychemistry.chemical_compoundZwitterionPolymer chemistryReaction pathPhysical and Theoretical ChemistryCobaltOrganometallics
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Formation, structure and reactivity of boryloxycarbyne complexes of group 6 metals.

2003

Reaction of the diborane(4) B(2)(NMe(2))(2)I(2) with two equivalents of K[(eta(5)-C(5)H(5))M(CO)(3)] (M=Cr, Mo, W) yielded the dinuclear boryloxycarbyne complexes [[(eta(5)-C(5)H(5))(OC)(2)M(triple bond)CO](2)B(2)(NMe(2))(2)] (4 a, M=Mo; b, M=W; c, M=Cr), which were fully characterised in solution by multinuclear NMR methods. The Mo and W complexes 4 a, b proved to be kinetically favoured products of this reaction and underwent quantitative rearrangement in solution to afford the complexes [[(eta(5)-C(5)H(5))(OC)(2)M(triple bond)CO]B(NMe(2))B(NMe(2))[M(CO)(3)(eta(5)-C(5)H(5))]] (5 a, M=Mo; b, M=W); 5 a was characterised by X-ray crystallography in the solid state. Corresponding reactions of…

ChemistryOrganic ChemistryInorganic chemistrySolid-statechemistry.chemical_elementBoranesGeneral ChemistryMedicinal chemistryCatalysischemistry.chemical_compoundTransition metalGroup (periodic table)Reactivity (chemistry)BoronDiboraneChemistry (Weinheim an der Bergstrasse, Germany)
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Modes of complexation of non-substituted and substituted tetraazamacrocycles with Group 6 metal carbonyls. X-ray structure of [(permethylcyclam)Mo(CO…

1995

Abstract Reactions of complexation of tetraazamacrocycles L with Group 6 metal carbonyls [M(CO)6](M = Cr, Mo, or W) lead to [LM(CO)4], [LM(CO)3] or [LM(CO)2] entities, depending both on the size of the macrocycle and on the metal M. The structure of one representative complex [(permethylcyclam)Mo(CO)4] has been determined by X-ray diffraction (permethylcyclam: 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane).

ChemistryOrganic ChemistryX-raychemistry.chemical_elementMetal carbonylTungstenBiochemistryInorganic ChemistryMetalCrystallographyChromiumGroup (periodic table)Molybdenumvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Structural and conductivity studies in LiFeP 2 O 7 , LiScP 2 O 7 , and NaScP 2 O 7

2000

Structural studies of LiScP2O7 by Rietveld refinement confirm that this material is isostructural with LiFeP2O7 studied previously. However, NaScP2O7 shows a structure different from the structural types of the basic group of NaIMIIIP2O7 known thus far. Systematic ranges for the six structural types of AIMIIIP2O7 are presented in terms of ion radii sums and ratios. The framework of LiMP2O7 (M=Sc, Fe) has rather wide tunnels running along the crystallographic c-axis. This feature has determined our interest to check the ion conductivity in AIMIIIP2O7 (A=Li, Na; M=Sc, Fe). The bulk conductivity, however, is low in these compounds, 10−6–10−7 S/cm at 300 °C, as determined by impedance spectrosc…

ChemistryRietveld refinementInorganic chemistryAnalytical chemistrychemistry.chemical_elementConductivityCondensed Matter PhysicsElectrochemistryIonDielectric spectroscopyGroup (periodic table)ElectrochemistryGeneral Materials ScienceLithiumElectrical and Electronic EngineeringIsostructuralJournal of Solid State Electrochemistry
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EFFECT OF HOT AIR TREATMENT ON MINIMALLY PROCESSED CAULIFLOWER

2013

The request of minimally processed vegetable is continuously increasing, and there is a growing interest for new fresh cut products. Cauliflower, as other cabbages, is highly appreciated for its nutritional value due to the good content of vitamins, antioxidants and anti-carcinogenic compounds. It is suitable to be used as a minimally processed vegetable, but harvesting and the following processing can cause a severe stress determining the appearance of accelerated senescence symptoms. The aim of the present work was to investigate the effect of hot air treatment and cold storage on minimally processed green cauliflower. Fresh-cut cauliflower florets put in sealed PE bags were treated at 48…

ChemistrySoluble solidsAir treatmentCold storageFresh-cut vegetables Brassica oleracea L. var. botrytis L. postharvest treatments cold storage browningTitratable acidSettore AGR/04 - Orticoltura E FloricolturaFood scienceHorticultureActa Horticulturae
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Use of Nanomaterials as Alternative for Controlling Enzymatic Browning in Fruit Juices

2020

Abstract Polyphenol oxidase (PPO) enzyme, present in most of fruits and vegetables, frequently induces browning in juices and beverages during postharvest and processing. Many efforts have been done to prevent or avoid this reaction. Nevertheless, the development of new methods is still of interest since many of the current methods present important drawbacks. An overview of the exiting techniques to inhibit enzymatic browning has been compiled in this chapter, including physical (i.e., thermal treatments, high pressures, irradiation, ultrasonication, pulsed electric fields, and ultrafiltration) and chemical techniques (acidification, addition of antibrowning agents) but with particular att…

ChemistrySonicationFruits and vegetablesBrowningUltrafiltrationPostharvestFood sciencePolyphenol oxidaseSilver nanoparticleNanomaterials
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Profiling of RNA modifications by multiplexed stable isotope labelling

2014

The combination of (15)N/(13)C stable isotope labelling (SIL) and LC-MS/MS revealed a total of 52 modifications in RNA from E. coli and yeast, including 10 previously undescribed modifications. Two modifications, N-ribosylnicotinamide and 2-methylthioadenosine, were newly detected in species hitherto thought not to contain these modifications.

ChemistryStable isotope ratioMetals and AlloysRNASaccharomyces cerevisiaeGeneral ChemistryTandem mass spectrometryCatalysisYeastSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiochemistryTandem Mass SpectrometryIsotope LabelingLabellingEscherichia coliMaterials ChemistryCeramics and CompositesRNAChromatography LiquidChemical Communications
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