Search results for "Reversible process"

showing 6 items of 6 documents

Controlling the Host-Guest Interaction Mode through a Redox Stimulus

2017

International audience; A proof-of-concept related to the redox-control of the binding/releasing process in a host-guest system is achieved by designing a neutral and robust Pt-based redox-active metallacage involving two extended-tetrathiafulvalene (exTTF) ligands. When neutral, the cage is able to bind a planar polyaromatic guest (coronene). Remarkably, the chemical or electrochemical oxidation of the host-guest complex leads to the reversible expulsion of the guest outside the cavity, which is assigned to a drastic change of the host-guest interaction mode, illustrating the key role of counteranions along the exchange process. The reversible process is supported by various experimental d…

010405 organic chemistryStereochemistrySupramolecular chemistryGeneral MedicineGeneral ChemistryReversible processself-assembly010402 general chemistryElectrochemistry01 natural sciencesRedoxsupramolecular cageCatalysisCoronene0104 chemical scienceschemistry.chemical_compoundchemistryChemical physicsDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySelf-assemblyTetrathiafulvaleneexTTF
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On the Existence of Different Zeolite-Associated Topological Redox Isomers. Electrochemistry of the Y Zeolite-Associated Mn(Salen)N3 Complex

2002

The electrochemical properties of Y zeolite-associated MnIII(salen)N3 (salen = trans-(R,R)-1,2-bis(salicyldeneamino)cyclohexane) has been investigated using polymer film electrodes immersed into neutral aqueous solutions. Zeolite Y-associated Mn(III)−salen complexes are reduced in one-electron reversible process at −0.25 V versus SCE. The electrochemical response is discussed in terms of the existence of two topological redox isomers:  a weakly boundary-associated Mn(salen) complex, whose electrochemical response corresponds to a reversible one-electron transfer controlled by diffusion of the positive ions of the supporting electrolyte through the zeolite surface windows and channels, and a…

Aqueous solutionCyclohexaneSupporting electrolyteInorganic chemistryReversible processTopologyElectrochemistryRedoxSurfaces Coatings and Filmschemistry.chemical_compoundchemistryMetal salen complexesMaterials ChemistryPhysical and Theoretical ChemistryZeoliteThe Journal of Physical Chemistry B
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Coherence absorption and condensation induced by thermalization of incoherent nonlinear fields

2008

We show that a conservative system of incoherent nonlinear waves exhibits, as a rule, an irreversible process of coherence transfer, in which the incoherence of the system is absorbed by the small-amplitude field, thus allowing the high-amplitude field to evolve towards a highly condensed coherent state. This process of coherence absorption results from the natural thermalization of the fields to a thermodynamic equilibrium state. The theory reveals that, contrary to a classical gas system, a wave system does not satisfy an equipartition of energy among the particles. Such a distinctive feature is the key property underlying the existence of the coherence absorption process. The coherence a…

Irreversible processPhysicsThermalisationThermodynamic equilibriumQuantum mechanicsGeneral Physics and AstronomyCoherent statesDegree of coherenceQuantumEquipartition theoremCoherence (physics)EPL (Europhysics Letters)
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Small-angle x-ray scattering studies of melting

1980

The course of melting of melt-crystallized polyethylene fractions and of a poly(ethylene oxide)-polystyrene-poly(ethylene oxide) triblock copolymer has been followed by small-angle x-ray scattering (SAXS). Changes in the intensity and shape of the SAXS curves indicated that both surface melting and melting over the full crystallite thickness (full-strand melting) take place. Full strand melting is the final, irreversible process. Comparison with an analytical model indicates that in the earlier stages of the irreversible, full-strand process the crystallites melt out randomly throughout the bulk. Later stages may occur by the simultaneous melting of a larger stack of crystallites.

Materials scienceEthylene oxideScatteringSmall-angle X-ray scatteringGeneral EngineeringAnalytical chemistryPolyethyleneIrreversible processchemistry.chemical_compoundCrystallographychemistryCopolymerCrystalliteMelting-point depressionJournal of Polymer Science: Polymer Physics Edition
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Towards a nonequilibrium thermodynamic description of incoherent nonlinear optics

2007

pa href="http://oe.osa.org/virtual_issue.cfm?vid=36"Focus Serial: Frontiers of Nonlinear Optics/a/pThis concise review is aimed at providing an introduction to the kinetic theory of partially coherent optical waves propagating in nonlinear media. The subject of incoherent nonlinear optics received a renewed interest since the first experimental demonstration of incoherent solitons in slowly responding photorefractive crystals. Several theories have been successfully developed to provide a detailed description of the novel dynamical features inherent to partially coherent nonlinear optical waves. However, such theories leave unanswered the following important question: Which is the long term…

PhysicsWave propagationbusiness.industryThermodynamic equilibriumNon-equilibrium thermodynamicsOptical field01 natural sciencesAtomic and Molecular Physics and Optics010305 fluids & plasmasIrreversible processOpticsQuantum mechanicsNonlinear medium0103 physical sciencesThermodynamic limitCoherent states010306 general physicsbusinessComputingMilieux_MISCELLANEOUS
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Mononuclear isoheterocyclic rearrangements. Note I. Interconversion of 3-benzoylamino-5-methyl-1,2,4-oxadiazole and 3-acetylamino-5-phenyl-1,2,4-oxad…

1975

The first example of mononuclear isoheterocyclic rearrangement is reported. The 3-benzoylamino-5-methyl-1,2,4-oxadiazole (5) furnishes through a reversible process (slowly at room temperature in methanol, acetone or dioxane, fast in DMSO or in methanol in the presence of strong bases) a mixture of 5 and 3-acethylamino-5-phenyl-1,2,4-oxadiazole (6). The equilibrium process can be achieved also by heating 5 at 181° and the same reaction mixture can be obtained using 6 as the starting material. 3-Trichloroacetylamino-5-methyl-1,2,4-oxadiazole (7) was unaffected by similar treatment. The results obtained are discussed.

chemistry.chemical_compoundchemistryOrganic ChemistryAcetoneOxadiazoleOrganic chemistryReversible processMethanolMedicinal chemistryJournal of Heterocyclic Chemistry
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