Circular dichroism in angle-resolved photoemission spectra of under- and overdoped Pb-Bi2212

We use angle-resolved photoemission with circularly polarized excitation to demonstrate that in the 5 x 1 superstructure-free (Pb,Bi)(2)Sr(2)CaCu(2)O(8+delta) (Pb-Bi2212) material there are no signatures of time-reversal symmetry breaking in the sense of the criteria developed earlier [Nature (London) 416, 610 (2002)]]. The dichroic signal retains reflection antisymmetry as a function of temperature and doping and in all mirror planes, precisely defined by the experimental dispersion at low energies. The obtained results demonstrate that the signatures of time-reversal symmetry violation in pristine Bi2212, as determined by angle-resolved photoemission spectroscopy, are not a universal feature of all cuprate superconductors.     

Circular dichroism in laser-assisted short-pulse photoionization

A remarkable effect of circular dichroism, i.e., a difference in photoelectron spectra produced by right and left circularly polarized light in two-color multiphoton ionization of atoms, is predicted for the case when the atom is ionized by an extreme ultraviolet or x-ray femtosecond pulse in the field of a strong infrared laser pulse, both pulses being circularly polarized. We show that the sidebands formed in the spectra exhibit different circular dichroism often of different signs both in angle-resolved and angle-integrated experimental conditions. The effect can be used for detecting and measuring circular polarization of x rays in a spectral range where other methods are not effective.     

Contribution to the study of photoanisotropy in azo dyes

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 52, No. 2, pp. 280–284, February, 1990.     

Interaction between flavin mononucleotide-containing azoreductase and azo dyes

ABSTRACT

Azoreductase, a flavin mononucleotide-containing oxidoreductase from Escherichia coli, can catalyze the reduction of azo dyes to form aromatic amine compounds. Few spectroscopic studies have explored the binding mode of azo dyes or the role of the arginine at site 59 in Azoreductase. In this article, protein engineering strategy has been used to construct one mutant in which the arginine residue at site 59 was mutated to glycine. Fluorescence spectroscopic data showed that the addition of Methyl Red and Methyl Orange resulted in the fluorescence quenching of the cofactor flavin mononucleotide bound to Azoreductase. The association constant was fitted using the standard binding equation instead of the Stern-Volmer equation. The results showed that the mutation from the arginine to glycine at site 59 weakened the association constant from 2.21?×?10⁵?L.mol^?1 to 4.55?×?10⁴?L.mol^?1 at 25°C. A similar phenomenon was also observed when Methyl Orange was used as a substrate. In each case, the association constant tended to decrease as the temperature increased from 25°C to 37°C. Thermodynamic parameter analysis revealed that the interaction type changed from a van der Waals interaction (between Azoreductase and the dyes) to a hydrogen bonding interaction (between the mutant and the dyes). Moleculcar docking was also performed in this work to provide some support for the binding mode and binding stability between Azoreductase/mutant and azo dyes.     

Polarization effects in photoisomerization of azo dyes in polymeric films

The reversible cis-trans photoisomerization of disperse red 1 (DR1) in PMMA thin films has been demonstrated previously by using the Attenuated Total Reflection (ATR) method. In this communication photoisomerization of DR1 is shown to be strongly polarization sensitive. This new property of dye doped polymeric films could lead to practical applications in integrated optics. A simple molecular interpretation is given. Illumination of a DR1 sample by polarization fringes produces a grating of molecular orientation able to diffract a probe beam.     

Circular dichroism of planar chiral magnetic metamaterials

We propose, fabricate, and study a double-layer chiral planar metamaterial that exhibits pronounced circular dichroism at near-infrared wavelengths. The antisymmetric oscillation modes of the two coupled layers allow local magnetic-dipole moments and enhanced polarization effects compared with similar single-layer systems where only electric-dipole moments occur. Experiment and rigorous theoretical calculations are in good agreement.     

Circular dichroism in radiative and nonradiative inelastic XUV scattering

Accepted: 6 March 1997     

Molecular magnetic dichroism in spectra of white dwarfs

We present novel calculations of the magnetic dichroism appearing in molecular bands in the presence of a strong magnetic field, which perturbs the internal structure of the molecule and results in net polarization due to the Paschen-Back effect. Based on that, we analyze new spectropolarimetric observations of the cool magnetic helium-rich white dwarf G99-37, which shows strongly polarized molecular bands in its spectrum. In addition to previously known molecular bands of the C2 Swan and CH A-X systems, we find a firm evidence for the violet CH B-X bands at 390 nm and C2 Deslandres-d'Azambuja bands at 360 nm. Combining the polarimetric observations with our model calculations, we deduce a dipole magnetic field of 7.5+/-0.5 MG with the positive pole pointing towards the Earth. We conclude that the developed technique is an excellent tool for studying magnetic fields on cool magnetic stars.     

Study of structural factors influencing the weigert effect in azo dyes

Experimental data that make it possible to correlate the photoanisotropic properties of materials based on azo dyes with their molecular structure are reported. Conclusions are drawn allowing one to predict, based on the structural formulas of dye molecules, their ability to induce photoanisotropy. Specially synthesized dyes were used and predictions are made regarding optimization of dyes with required photoanisotropic parameters.     

Circular dichroism induced by Fano resonances in planar chiral oligomers

We present a general theory of circular dichroism in planar chiral nanostructures with rotational symmetry. It is demonstrated, analytically, that the handedness of the incident field's polarization can control whether a nanostructure induces either absorption or scattering losses, even when the total optical loss (extinction) is polarization‐independent. We show that this effect is a consequence of modal interference so that strong circular dichroism in absorption and scattering can be engineered by combining Fano resonances with planar chiral nanoparticle clusters.

     

Sonochemical degradation of azo dyes in aqueous solution: a new heterogeneous kinetics model taking into account the local concentration of OH radicals and azo dyes

The sonochemical decolorization and decomposition of azo dyes, such as C. I. Reactive Red 22 and methyl orange, were performed from the viewpoints of wastewater treatment and to determine the reaction kinetics. A low concentration of the azo dye solution was irradiated with a 200 kHz and 1.25 W/cm2 ultrasound in a homogeneous aqueous solution. The azo dye solutions were readily decolorized by the irradiation. The sonochemical decolorization was also depressed by the addition of the t-butyl alcohol radical scavenger. These results indicated that azo dye molecules were mainly decomposed by OH radicals formed from the water sonolysis. In this paper, we propose a new kinetics model taking into account the heterogeneous reaction kinetics similar to a Langmuir-Hinshelwood mechanism or an Eley-Rideal mechanism. The proposed kinetics model is based on the local reaction site at the interface region of the cavitation bubbles, where azo dye molecules are quickly decomposed because an extremely high concentration of OH radicals exists in this region. To confirm the proposed kinetics model, the effects of the initial concentration of azo dyes, irradiated atmosphere and pH on the decomposition rates were investigated. The obtained results were in good agreement with the proposed kinetics model.     

Circular dichroism in biological photonic crystals and cubic chiral nets

Nature provides impressive examples of chiral photonic crystals, with the notable example of the cubic so-called srs network (the label for the chiral degree-three network modeled on SrSi2) or gyroid structure realized in wing scales of several butterfly species. By a circular polarization analysis of the band structure of such networks, we demonstrate strong circular dichroism effects: The butterfly srs microstructure, of cubic I4(1)32 symmetry, shows significant circular dichroism for blue to ultraviolet light, that warrants a search for biological receptors sensitive to circular polarization. A derived synthetic structure based on four like-handed silicon srs nets exhibits a large circular polarization stop band of a width exceeding 30%. These findings offer design principles for chiral photonic devices.