Search results for "Lamellar structure"

showing 10 items of 85 documents

ChemInform Abstract: New Trends in V-P-O Solids

2010

On the basis of the industrial interest of the oxovanadium phosphate catalysts, current research effort in this field is focused mainly on the development of synthetic strategies directed towards obtaining open-framework materials. There is a growing body of work describing preparations using hydrothermal procedures under a diversity of conditions. A great number of new solids, whose nets range from lamellar arrays to micro- and mesostructured organizations, has been prepared in last years. In this context, the applicability of concepts and procedures from the zeolites chemistry to systems involving transition elements is critically analyzed.

ChemistryNanotechnologyLamellar structureContext (language use)General MedicineChemInform
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Symmetric diblock copolymers confined into thin films: A Monte Carlo investigation on the CRAY T3E

2000

We present the results of large scale computer simulations targeted at investigating the phase stability and the structure of symmetric AB diblock copolymers in thin films. The connectivity of the two different monomer species A and B in the diblock copolymer prevents macrophage separation and the molecules assemble into A-rich and B-rich domains on the scale of the molecule’s extension. This large length scale of the ordering phenomena makes these polymeric systems a promising candidate for revealing the universal features of self-assembling in amphiphilic molecules. However, the widely spread length and time scales impart protracted long relaxation times to the systems and pose a challeng…

Condensed Matter::Soft Condensed MatterLength scaleCapillary waveMaterials scienceChemical physicsRelaxation (NMR)Monte Carlo methodPerpendicularMoleculeLamellar structureThin film
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α, ω-Dipolar amphiphiles: Influence of rigid and flexible units on aggregation behavior

1993

Mono- and α,ω-dipolar amphiphiles with hydrophilic pyridinium head groups, and flexible and rigid hydrophobic parts have been synthesized. Surface tension and conductivity measurements proved that micellar aggregates for amphiphiles 1–4 are formed. The incorporation of rigid units leads to a decrease in the critical micellar concentration (CMC): the rigid monopolar amphiphile 2 aggregates at lower concentration than the flexible monopolar amphiphile 1. A similar decrease was observed when chain ends were connected: the flexible α,ω-dipolar amphiphile 3 has a lower CMC than the flexible monopolar amphiphile 1. The more flexible amphiphiles 1–3 allow the formation of micelles of different sha…

CrystallographyLiquid crystalChemistryCritical micelle concentrationLyotropicAmphiphileMesophaseOrganic chemistryMicellar cubicLamellar structureGeneral ChemistryMicelleRecueil des Travaux Chimiques des Pays-Bas
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The Phase Behaviour of Amphiphilic Monolayers

1991

Amphiphilic monolayers display a wealth of condensed phases. It is only recently that these have been widely recognised as being distinct, but they are in fact quite analogous to the well-known lamellar gel phases of bulk lyotropic and thermotropic mesogens. An understanding of these phases has proved to be important for controlling the defect structure of the monolayers used in the fabrication of Langmuir-Blodgett films. This understanding is being achieved by developments in a number of techniques, including X-ray diffraction and isotherm miscibility. The phase diagrams of the materials studied so far are all very closely related, lending new credibility to the principle of corresponding …

CrystallographyPhase transitionMaterials scienceLiquid crystalChemical physicsGeneral Chemical EngineeringPhase (matter)MonolayerLyotropicLamellar structureThermotropic crystalPhase diagramBerichte der Bunsengesellschaft für physikalische Chemie
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Toward new organic/inorganic superlattices: Keggin polyoxometalates in Langmuir and Langmuir-Blodgett films

1997

The effect of Keggin heteropolyoxotungstates (XW12O40n- with X = H2, P, Si, B or Co) on Langmuir films has been studied for monolayers of DODA (dimethyldioctadecylammonium) and DPPC (1,2-dipalmitoyl-sn-glycero-3-phosphorylcholine). Marked modifications of the compression isotherms have been observed when the Keggin anions were dissolved in the subphase:  this demonstrates that the polyanions interact with the monolayer. Langmuir−Blodgett (LB) films have been readily obtained from these systems (even with DPPC) for a particular range in polyanion concentration. X-ray diffraction and infrared dichroism experiments have shown a well-defined lamellar structure for these built-up films as well a…

DiffractionLangmuirChemistrySuperlatticeSurfaces and InterfacesCondensed Matter PhysicsElectric chargeLangmuir–Blodgett filmCrystallographyMonolayerOrganic inorganicElectrochemistryOrganic chemistryGeneral Materials ScienceLamellar structureSpectroscopy
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Stabilization of the monoolein Pn 3 m cubic structure on trehalose glasses

1999

Trehalose is known to protect some organisms from various stresses due to drought and high temperature. To explore the molecular mechanism of the protective function, the mesomorphic properties of the monoolein-water system, dried in the presence of trehalose, were studied by X-ray diffraction. While, in pure water, two bicontinuous inverse cubic structures (the Pn3m and Ia3d phases) and a lamellar Lα phase exist as a function of concentration, only the Pn3m cubic phase has been detected in concentrated trehalose solutions or in trehalose glasses, even under extremely dry conditions. Depending on the sugar concentration, or after glass dehydration, the Pn3m cubic unit cell decreases to very…

DiffractionPhase transitionMaterials scienceBiophysicsGeneral Medicinemedicine.diseaseTrehalosechemistry.chemical_compoundCrystallographychemistryChemical physicsPhase (matter)X-ray crystallographymedicineLamellar structureDehydrationSugarEuropean Biophysics Journal
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Bio-sintering processes in hexactinellid sponges: Fusion of bio-silica in giant basal spicules from Monorhaphis chuni☆

2009

The two sponge classes, Hexactinellida and Demospongiae, comprise a skeleton that is composed of siliceous skeletal elements (spicules). Spicule growth proceeds by appositional layering of lamellae that consist of silica nanoparticles, which are synthesized via the sponge-specific enzyme silicatein. While in demosponges during maturation the lamellae consolidate to a solid rod, the lamellar organization of hexactinellid spicules largely persists. However, the innermost lamellae, near the spicule core, can also fuse to a solid axial cylinder. Similar to the fusion of siliceous nanoparticles and lamella, in several hexactinellid species individual spicules unify during sintering-like processe…

FusionSpiculebiologyHexactinellidMolecular Sequence DataAnimal StructuresAnatomyBlotting NorthernSilicon Dioxidebiology.organism_classificationPoriferaSpongeLamella (surface anatomy)Sponge spiculeStructural BiologySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationComplementary DNAMicroscopy Electron ScanningBiophysicsAnimalsLamellar structureJournal of Structural Biology
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Synthesis and Crystal Structure of a Novel Lamellar Barium Derivative:  Ba(VOPO4)2·4H2O. Synthetic Pathways for Layered Oxovanadium Phosphate Hydrate…

1997

A unified synthetic strategy has allowed us to rationalize the preparative chemistry of the layered oxovanadium phosphates M(VOPO4)2·nH2O. Thus, we have been able to isolate as single phases with reasonable yields both all the previously characterized phosphates and a new solid containing Ba2+ cations as guest species as well as to prepare new related derivatives involving arsenate anions. In order to organize the experimental results, we have used two complementary models:  a simple restatement of the partial charge model (PCM), and the valence matching principle (VMP) (derived from the bond valence method). The crystal structure of the new barium lamellar derivative, Ba(VOPO4)2·4H2O, has …

Inorganic ChemistryPartial chargeCrystallographyValence (chemistry)chemistryBond valence methodchemistry.chemical_elementLamellar structureBariumCrystal structurePhysical and Theoretical ChemistrySingle crystalMonoclinic crystal systemInorganic Chemistry
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Prediction of Magnetic Properties in Oxovanadium(IV) Phosphates: The Role of the Bridging PO4 Anions

1998

Oxovanadium phosphates constitute a crystallochemically very rich family that, in turn, results in a seemingly intricate magnetochemistry including from isolated dimers to 3-D systems. This magnetic diversity is due, in part, to the possible participation of phosphate groups in the spin transfer between VIV centers. This way, 31P solid-state NMR becomes a key tool in determining the exchange paths involving phosphorus orbitals. The magnetic behavior of several layered oxovanadium phosphates M(VOPO4)2·4H2O (M = Na+, Ca2+, Ba2+, and Pb2+) has been investigated. Like it occurs in the case of other previously studied lamellar derivatives, the best fit of the temperature-dependent magnetic susce…

Inorganic Chemistrychemistry.chemical_compoundCrystallographychemistryAtomic orbitalMagnetochemistrySpin transferLamellar structureOxovanadium IVPhysical and Theoretical ChemistryPhosphateMagnetic susceptibility
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Synthesis of a new mesostructured lamellar oxovanadium phosphate assembled through an S+X-I0 Mechanism

1999

A new lamellar mesostructured oxovanadium(V) phosphate, (DDAH)0.9(Cl)0.9VOPO4·1.5H2O (DDA = dodecylamine), has been synthesized through a S+X-I0 cooperative mechanism using protonated dodecylamine ...

Inorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryOrganic chemistryLamellar structureProtonationPhysical and Theoretical ChemistryPhosphate
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