Search results for "SITES"

showing 10 items of 2851 documents

Organic chelate-free and azido-rich metal clusters and coordination polymers from the use of Me3SiN3: a new synthetic route to complexes with beautif…

2019

In this Feature Article, we highlight the feasibility of a new, recently developed approach towards the synthesis of high-spin molecules and single-molecule magnets (SMMs). The key to the preparation of such molecular compounds is the organic azide precursor Me3SiN3, which fosters the formation of 3d-metal azido clusters and coordination polymers without requiring the assistance of any organic chelating/bridging group. All the isolated compounds contain metallic cores which are surrounded by end-on bridging N3− groups. Consequently, the reported molecular materials exhibit ferromagnetic exchange interactions between the spin carriers, resulting in the stabilization of the maximum possible s…

chemistry.chemical_classification010405 organic chemistryMetals and AlloysGeneral ChemistryPolymer010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCoordination complexMetalchemistry.chemical_compoundMagnetic anisotropyFerromagnetismchemistryvisual_artReagentMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumMoleculeAzideChemical Communications
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Selective precipitation of alkyl dihalides using a newly synthesized water-soluble bisphosphorylpillar[5]arene

2016

Bisphosphorylpillar[5]arenes ( and ) were synthesized and used to study the host-guest complexation in organic solvents and water. The interactions between the guests and the phosphate of the hosts lead to strong binding towards alkyl dihalides and alkyldiammonium ions. may be used to detect or separate alkyl dihalides in water due to the rapid precipitation of the complex.

chemistry.chemical_classification010405 organic chemistryPrecipitation (chemistry)Metals and AlloysGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWater solublechemistryMaterials ChemistryCeramics and CompositesOrganic chemistryAlkylChemical Communications
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Evidence for essential primary amino groups in a bacterial coupling factor F1ATPase.

1980

Abstract We have found that the binding of pyridoxal-5′-phosphate to 6 primary amino groups leads to the inactivation of the enzyme. A preferential reaction of pyridoxal-5′-phosphate with the α-subunits of this enzyme can be demonstrated. The reactivity of the amino groups is influenced by various effectors. In the presence of ATP the inhibition of the ATPase activity is noncompetitive.

chemistry.chemical_classificationAdenosine TriphosphatasesPrimary (chemistry)Binding SitesChemistryStereochemistryEffectorCell MembraneBiophysicsCell BiologyBiochemistryMicrococcusCoupling (electronics)Structure-Activity RelationshipEnzymeBiochemistrySolubilityPyridoxal PhosphateAtpase activityReactivity (chemistry)Amino AcidsMolecular BiologyBiochemical and biophysical research communications
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Single particle jumps and correlated ionic motions in glass-ceramics

1993

Using impedance spectroscopy, the ion transport in poorly Li-conducting aluminosilicate glass ceramics and their precursor glasses has been measured for temperatures 50 K < T < 550 K and covering a frequency range of more than 14 decades from 10 mHz up to 3 THz. In addition to the familiar cooperative ionic motion dominating at high temperatures, for the first time dielectric relaxation due to elementary hopping processes is observed well below room temperature.

chemistry.chemical_classificationAnalytical chemistryMineralogyIonic bondingCondensed Matter Physics530Electronic Optical and Magnetic MaterialsDielectric spectroscopychemistryAluminosilicatevisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumIonic conductivityParticleDielectric lossCeramicInorganic compound
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Study of morphology, mechanical properties, and thermal degradation of polycarbonate-titania nanocomposites as function of titania crystalline phase …

2013

Titania nanoparticles were prepared using a sol–gel method and calcination at 2008C and 6008C to obtain anatase and rutile phases, respectively. The obtained powders were used to prepare polycarbonate (PC)-titania nanocomposites by melt compounding. The effect of different crystalline phases and amounts of titania, in the range 1–5 wt%, on the morphology, mechanical properties, and thermal degradation kinetics of PC was investigated. The results show that the filler modified the plasticity or rigidity of the polymer and influenced the degradation kinetics, in different ways depending on the type and amount of titania. POLYM. COMPOS.,

chemistry.chemical_classificationAnataseMaterials scienceNanocompositePolymers and PlasticsGeneral ChemistryPolymerPlasticitylaw.inventionchemistrylawRutileCompoundingvisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumCalcinationPolycarbonateComposite materialPolymer Composites
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Low-Temperature Optical Spectroscopy of Native and Azide-Reacted Bovine Cu,Zn Superoxide Dismutase. A Structural Dynamics Study

1994

The optical absorption spectra of native and N(3-)-reacted Cu,Zn superoxide dismutase (SOD) has been studied in the temperature range 300-10 K. The broad d-d bands observed in the room temperature spectrum, centered at 14,700 cm-1 (native enzyme) and at 15,550 cm-1 (N(3-)-reacted enzyme), are clearly split at low temperature into two bands each, centered at 12,835 and 14,844 cm-1 and at 14,418 and 16,300 cm-1, respectively. The thermal behavior of the 23,720 cm-1 band present in the spectrum of the native enzyme indicates that this band belongs to the His61-->Cu(II) ligand to metal charge transfer transition. Analysis of the zeroth, first, and second moments of the various bands as a functi…

chemistry.chemical_classificationAzidesBinding SitesHot TemperatureSuperoxide DismutaseLigandCircular DichroismTemperatureAtmospheric temperature rangeBiochemistryIonCatalysisMetalchemistry.chemical_compoundCrystallographyEnzymechemistrySpectrophotometryvisual_artvisual_art.visual_art_mediumAnimalsCattleAzideSpectroscopyCopperBiochemistry
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Fine tuning of the catalytic effect of a metal-free porphyrin on the homogeneous oxygen reduction.

2011

The catalytic effect of tetraphenylporphyrin on the oxygen reduction with ferrocene in 1,2-dichloroethane can be finely tuned by varying the molar ratio of the acid to the catalyst present in the solution. The mechanism involves binding of molecular oxygen to the protonated free porphyrin base, in competition with ion pairing between the protonated base and the acid anion present.

chemistry.chemical_classificationBase (chemistry)Inorganic chemistryMetals and AlloysProtonationGeneral ChemistryPhotochemistryPorphyrinCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundElectron transferchemistryFerroceneTetraphenylporphyrinMaterials ChemistryCeramics and CompositesPerchloric acidChemical communications (Cambridge, England)
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Hybrid Molecular Materials Based upon Organic π-Electron Donors and Inorganic Metal Complexes. Conducting Salts of Bis(ethylenediseleno)tetrathiafulv…

2002

Abstract The synthesis, structure and physical characterization of three new radical salts formed by the organic donor bis(ethylenediseleno)tetrathiafulvalene (BEDS-TTF or BEST) and the paramagnetic hexacyanoferrate(III) anion [Fe(CN)6]3− or the photochromic nitroprusside anion [Fe(CN)5NO]2− are reported: (BEST)4[Fe(CN)6] (1), (BEST)3[Fe(CN)6]2·H2O (2) and (BEST)2[Fe(CN)5NO] (3). Salts 1 and 3 show a layered structure with alternating organic (β–type packing) and inorganic slabs. Salt 2 shows an original interpenetrated structure probably due to the unprecedented presence of (BEST)2+ dications. The three salts are semiconductors although salt 1 exhibits a high room temperature conductivity …

chemistry.chemical_classificationBicyclic moleculeInorganic chemistrySalt (chemistry)Crystal structureCondensed Matter PhysicsMolecular electronic transitionElectronic Optical and Magnetic MaterialsInorganic ChemistryMetalCrystallographychemistry.chemical_compoundOctahedronchemistryvisual_artMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumMoleculePhysical and Theoretical ChemistryTetrathiafulvaleneJournal of Solid State Chemistry
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Structural Properties of Carnation Mottle Virus p7 Movement Protein and Its RNA-binding Domain

2001

Plant viral movement proteins (MPs) participate actively in the intra- and intercellular movement of RNA plant viruses to such an extent that MP dysfunction impairs viral infection. However, the molecular mechanism(s) of their interaction with cognate nucleic acids are not well understood, partly due to the lack of structural information. In this work, a protein dissection approach was used to gain information on the structural and RNA-binding properties of this class of proteins, as exemplified by the 61-amino acid residue p7 MP from carnation mottle virus (CarMV). Circular dichroism spectroscopy showed that CarMV p7 is an alpha/beta RNA-binding soluble protein. Using synthetic peptides de…

chemistry.chemical_classificationBinding SitesCarlavirusC-terminusMolecular Sequence DataRNA-Binding ProteinsRNACell BiologyBiologyAlanine scanningBiochemistryProtein Structure SecondaryAmino acidViral ProteinsProtein structureBiochemistrychemistryRNAAmino Acid SequenceBinding siteMolecular BiologyPeptide sequenceBinding domainJournal of Biological Chemistry
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Proteolytic cleavage of soybean Bowman-Birk inhibitor monitored by means of high-performance capillary electrophoresis. Implications for the mechanis…

1996

The hydrolysis of the soybean Bowman-Birk inhibitor in the presence of catalytic amounts of bovine trypsin and the formation of the non-covalent enzyme-inhibitor complex with an equimolar amount of enzyme are monitored by means of high-performance capillary electrophoresis (HPCE). The inhibitor is cleaved in the trypsin-reactive and more slowly in the chymotrypsin-reactive subdomain. HPCE proves itself as the only reliable analytical tool to monitor these reactions in clear contrast to classical electrophoretic, chromatographic and enzymatic methods. The most efficient separation of the intact and the two active site cleaved forms of the inhibitor was achieved in borate buffer at pH 10.0. T…

chemistry.chemical_classificationBinding SitesChromatographybiologyChemistryHydrolysisMolecular Sequence DataBiophysicsElectrophoresis CapillaryActive siteCleavage (embryo)BiochemistryCatalysisProtein Structure TertiaryKineticsElectrophoresisHydrolysisReaction rate constantEnzymeCapillary electrophoresisBiochemistryEnzyme inhibitorbiology.proteinAmino Acid SequenceTrypsin Inhibitor Bowman-Birk SoybeanJournal of Biochemical and Biophysical Methods
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