Device for doubling the frequency of a light wave comprising a non-linear optical compound

The invention relates to a nonlinear optical medium and a device comprising such a nonlinear optical medium which can be suitably used to double the frequency of red light, while forming blue light. The nonlinear optical medium comprises a polymer matrix and nonlinear optical compounds which contain a substituted sulphone group as the electron-acceptor group

Nonlinear optical compound, nonlinear optical medium, method of manufacturing a nonlinear optical medium and device for doubling the frequency of a light wave

The invention relates to a nonlinear optical medium and a device comprising such a nonlinear optical medium which can be suitably used to double the frequency of red light, while forming blue light. The nonlinear optical medium comprises a polymer matrix and nonlinear optical compounds which contain a substituted sulphone group as the electron-acceptor group

Nonlinear optical compound, nonlinear optical medium, method of manufacturing a nonlinear optical medium and device for doubling the frequency of a light wave

The invention relates to a nonlinear optical medium and a device comprising such a nonlinear optical medium which can be suitably used to double the frequency of red light, while forming blue light. The nonlinear optical medium comprises a polymer matrix and nonlinear optical compounds which contain a substituted sulphone group as the electron-acceptor group

Device for doubling the frequency of a light wave comprising a non-linear optical compound

The invention relates to a nonlinear optical medium and a device comprising such a nonlinear optical medium which can be suitably used to double the frequency of red light, while forming blue light. The nonlinear optical medium comprises a polymer matrix and nonlinear optical compounds which contain a substituted sulphone group as the electron-acceptor group

Real time in-situ pulsed magnetic field coil deformation measurements with fiber Bragg sensors

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Nonresonant EFISH and THG studies of nonlinear optical property and molecular structure relations of benzene, stilbene, and other arene derivatives

D.c. elec. field induced 2nd-harmonic generation (EFISH) and 3rd-harmonic generation (THG) measurement results are reported on the intrinsic mol. hyperpolarizabilities of benzenes, stilbenes, and other arene derivs. Structure-property relations, as revealed by a comprehensive set of systematic measurements, are discussed. Issues concerning donor-acceptor strength; charge-transfer; transparency trade-off; conjugation planarity, length, and aromaticity; and heteroatom and side-group substitution effects are included

Colorless nonlinear optical D-p-A polymers with sulfones as electron acceptors

Colorless side-chain methacrylate copolymers exhibiting relatively narrow charge-transfer bands at 335 nm and second-order optical nonlinearities up to d33 = 4.3 pmV-1 (at 1064 nm) were synthesized and characterized. [on SciFinder (R)

Laser induced breakdown of the magnetic field reversal symmetry in the propagation of unpolarized light

We show how a medium, under the influece of a coherent control field which is resonant or close to resonance to an appropriate atomic transition, can lead to very strong asymmetries in the propagation of unpolarized light when the direction of the magnetic field is reversed. We show how EIT can be used to mimic effects occuring in natural systems and that EIT can produce very large asymmetries as we use electric dipole allowed transitions. Using density matrix calculations we present results for the breakdown of the magnetic field reversal symmetry for two different atomic configurations.Comment: RevTex, 6 pages, 10 figures, Two Column format, submitted to Phys. Rev.

Nonresonant EFISH And THG Studies Of Nonlinear Optical Property And Molecular Structure Relations Of Benzene, Stilbene, And Other Arene Derivatives.

D.c. elec. field induced 2nd-harmonic generation (EFISH) and 3rd-harmonic generation (THG) measurement results are reported on the intrinsic mol. hyperpolarizabilities of benzenes, stilbenes, and other arene derivs. Structure-property relations, as revealed by a comprehensive set of systematic measurements, are discussed. Issues concerning donor-acceptor strength; charge-transfer; transparency trade-off; conjugation planarity, length, and aromaticity; and heteroatom and side-group substitution effects are included

Electrical magnetochiral anisotropy in a bulk chiral molecular conductor

So far, no effect of chirality on the electrical properties of bulk chiral conductors has been observed. Introduction of chiral information in tetrathiafulvalene precursors represents a powerful strategy towards the preparation of crystalline materials in which the combination of chirality and conducting properties might allow the observation of the electrical magnetochiral anisotropy effect. Here we report the synthesis by electrocrystallization of both enantiomers of a bulk chiral organic conductor based on an enantiopure tetrathiafulvalene derivative. The enantiomeric salts crystallize in enantiomorphic hexagonal space groups. Single crystal resistivity measurements show metallic behaviour for the enantiopure salts down to 40 K, in agreement with band structure calculations. We describe here the first experimental evidence of electrical magnetochiral anisotropy in these crystals, confirming the chiral character of charge transport in our molecular materials