Photodissociation of CCH: classical trajectory calculations involving seven electronic states

The photodissociation dynamics of ethynyl radical, C(2)H, involving seven electronic states is studied by classical trajectory calculations. Initial values of the trajectories are selected based on relative absorption intensities calculated by Mebel et al. The energies and the derivatives are interpolated by three-dimensional cubic spline interpolator using an extended data pool. Mean square errors and standard deviations in interpolation of energies for 450 data points are found to be in the range 3.1 x 10(-6)-1.4 x 10(-5) and 1.7 x 10(-3)-3.8 x 10(-3) hartrees, respectively. The photofragments of C(2) and H are produced mainly in the X (1)Sigma(g) (+), a (3)Pi(u), b (3)Sigma(g) (-), c (3)Sigma(u) (+), A (1)Pi(u), B (1)Delta(g) electronic states of C(2) as product. The avoided crossings do not appear to be in the main dissociation pathways. The internal distributions are in good accord with the experimental results where comparison is possible, suggesting that the fragmentation mechanism of C(2)H(2) into C(2) and H is a two step process involving C(2)H radical as an intermediate with a life time long enough to allow complete collection of the phase space in the experiments.     

Real time inverse filter focusing through iterative time reversal

In order to achieve an optimal focusing through heterogeneous media we need to build the inverse filter of the propagation operator. Time reversal is an easy and robust way to achieve such an inverse filter in nondissipative media. However, as soon as losses appear in the medium, time reversal is not equivalent to the inverse filter anymore. Consequently, it does not produce the optimal focusing and beam degradations may appear. In such cases, we showed in previous works that the optimal focusing can be recovered by using the so-called spatiotemporal inverse filter technique. This process requires the presence of a complete set of receivers inside the medium. It allows one to reach the optimal focusing even in extreme situations such as ultrasonic focusing through human skull or audible sound focusing in strongly reverberant rooms. But, this technique is time consuming and implied fastidious numerical calculations. In this paper we propose a new way to process this inverse filter focusing technique in real time and without any calculation. The new process is based on iterative time reversal process. Contrary to the classical inverse filter technique, this iteration does not require any computation and achieves the inverse filter in an experimental way using wave propagation instead of computational power. The convergence from time reversal to inverse filter during the iterative process is theoretically explained. Finally, the feasibility of this iterative technique is experimentally demonstrated for ultrasound applications.     

Rifampicin inhibits alpha-synuclein fibrillation and disaggregates fibrils

The aggregation of alpha-synuclein in dopaminergic neurons of the substantia nigra is a critical step in the pathogenesis of Parkinson's disease. We show that the antibiotic rifampicin inhibited alpha-synuclein fibrillation and disaggregated existing fibrils in a concentration-dependent manner. Size-exclusion chromatography data indicated that rifampicin stabilized alpha-synuclein as both a monomer and soluble oligomers comprised of partially folded alpha-synuclein. Experiments using aged samples of rifampicin indicated that the most active species in inhibiting fibrillation and disaggregating fibrils is an oxidation product of rifampicin, which was confirmed in experiments under anaerobic conditions. These results indicate that rifampicin-mediated inhibition of alpha-synuclein fibrillation and disaggregation of fibrils involves preferential stabilization of monomeric and soluble oligomeric forms, and that rifampicin potentially may have therapeutic application for Parkinson's disease.     

Optical bistability in axially modulated OmniGuide fibers

We demonstrate the feasibility of optical bistability in an axially modulated nonlinear OmniGuide fiber through analytical theory and detailed numerical experiments. At 1.55-microm carrier wavelength, the in-fiber devices that we propose can operate with only a few tens of milliwatts of power, can have a nearly instantaneous response and recovery time, and can be shorter than 100 microm.     

Acoustical imaging through a multiple scattering medium using a time-reversal mirror

Acoustical imaging is based on the ability to focus an acoustic beam inside the zone of interest. This remains an issue through a high-order multiple scattering medium because the electronic delay lines that enable one to focus through a multiple scattering medium are a priori unknown. Using time-reversal principles, we show that images can be obtained through a very disordered medium. Surprisingly, the images are better than those obtained in a homogeneous medium with a classical imaging device.     

Complex dynamic behavior of fluctuating smectic- A films as studied by scattering with coherent X-rays

Coherent dynamic x-ray scattering has been used to study the thermally excited layer fluctuations in freely suspended smectic films of the compound 4O.8. Using 8-keV x rays and films with a thickness around 0.3 &mgr;m we resolve relaxation times down to a few &mgr;s. A combination of damped and oscillatory behavior is observed for the layer undulations, which can be attributed to inertial effects. These are due to the surface contribution to the free energy which cannot be disregarded for thin films.     

Joys and pitfalls of fermi surface mapping in Bi(2)Sr(2)CaCu(2)O(8+delta) using angle resolved photoemission

On the basis of angle-scanned photoemission data recorded using unpolarized radiation, with high (E,k) resolution, and an extremely dense sampling of k space, we resolve the current controversy regarding the normal state Fermi surface (FS) in Bi(2)Sr(2)CaCu(2)O(8+delta). The true picture is simple, self-consistent, and robust: the FS is holelike, with the form of rounded tubes centered on the corners of the Brillouin zone. Two further types of features are also clearly observed: shadow FSs, which are most likely to be due to short range antiferromagnetic spin correlations, and diffraction replicas of the main FS caused by passage of the photoelectrons through the modulated Bi-O planes.     

Hydrodynamics of nematic ferrofluids

The European Physical Journal E - We derive hydrodynamic equations for nematic ferrofluids (ferronematics) in the limit that the magnetic degree of freedom has relaxed to its equilibrium value. We...     

Zur Bestimmung von Doppelbindungsanteilen in Polyolefinen durch FTIR-Analyse

Zusammenfassung Im Rahmen von kinetischen Untersuchungen zur Olefinpolymerisation mußten geringe Doppelbindungskonzentrationen in Polymeren mit stark differierender Struktur und Konsistenz exakt bestimmt werden. Die quantitative FTIR-Analyse der unterschiedlichen Doppelbindungen wurde dadurch optimiert, daß die Substanzen in der Schmelze vermessen wurden, die IR-Bandengruppen mittels rechnerisch erzeugter Bandenprofile entzerrt und die integralen Absorbanzen der olefinischen Banden bestimmt wurden. Die durch Analyse von Modellsubstanzen ermittelten integralen Extinktionskoeffizienten, bezogen auf 1 cm Schichtdicke und auf eine Doppelbindung pro 10⁵ C-Atome liegen bei 0.93 (Vinyl), 0.95 (trans-Vinylen) und 1.04 (Vinyliden).

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Determination of double bond concentrations in polyolefines by FTIR analysis

Summary In the course of kinetic investigations on olefin polymerization it was necessary to measure the concentration of double bonds in polymers with very variable structure and consistency as exactly as possible. For that purpose, the quantitative FTIR-analysis of the different double bonds was optimized by measuring the melted substances, by analysis of the groups of IR-bands with the help of computer generated band profiles and by determing the integral absorbances of the olefinic bands. The integral extinction coefficients of the vinyl, the trans-vinylene and the vinylidene double bonds were determined by the analysis of model compounds and values of 0.93, 0.95 and 1.04, respectively, for a sample of 1 cm thickness with one double bond per 10⁵ carbon atoms were obtained.