Spin echoes in the charge transport through phosphorus donors in silicon

The electrical detection of spin echoes via echo tomography is used to observe coherent processes associated with the electrical readout of the spin state of phosphorus donor electrons in silicon near a SiO2 interface. Using the Carr-Purcell pulse sequence, an echo decay with a time constant of 1.7+/-0.2 micros is observed and discussed in terms of decoherence and recombination times. Electrical spin echo tomography thus can be used to study the dynamics of the spin-dependent transport processes, e.g., in realistic spin qubit devices for quantum information processing.     

On lineγ-Ray emission following 30 MeV/A12C induced reactions on some medium-heavy targets

Preliminary results on residual nuclei production in 30 MeV/A¹²C interaction with medium heavy targets are presented. Gamma-ray spectroscopic techniques were used. Evidence for charge and angular momentum transfer is found.

     

Level structure of 100Tc

Gamma and electron spectra following thermal neutron capture on ⁹⁹Tc have been studied with a bent-crystal spectrometer, Ge(Li) and Si(Li) detectors and a magnetic spectrometer. Prompt and delayed γ-γ coincidences with Ge(Li) detectors have been performed. A level scheme is proposed for ¹⁰⁰Tc comprising 21 excited states up to 640 keV. The binding energy of the last neutron in ¹⁰⁰Tc was deduced. For most levels, spin and parity values were assigned. Two isometric transitions of respective half-lives 10.2 and 4.6 μs have been identified using the ¹⁰⁰Mo(d, 2n)¹⁰⁰Tc reaction with a pulsed beam of deuterons. From the comparison of the present (n, γ) study and the collaborative study of the ⁹⁹Tc(d, p) reaction, several members of the multiplets $\text{π}\text{g}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}\text{ν}\text{g}{}_{\mathrm{<mtext>7</mtext><mtext>2</mtext>}}$, $\text{π}\text{g}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}\text{ν}\text{g}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$, $\text{π}\text{g}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}\text{ν}\text{s}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ and $\text{π}\text{p}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{ν}\text{d}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ have been identified.     

Charge injection and photooxidation of single conjugated polymer molecules

The complex, coupled mechanisms of charge transfer and oxidative damage in organic electronic devices (such as organic light-emitting diodes (OLED), solar cells, etc.) have been elucidated by a new technique that combines single-molecule spectroscopy with charge injection from a metal electrode. The experiments employed a sandwich device architecture (Au/TPD/MEH-PPV:PMMA/SiO2/ITO), essentially a modified OLED with a charge-blocking layer (SiO2) to suppress charge injection at the ITO electrode. The fluorescence (photoluminescence) of isolated MEH-PPV conjugated polymer molecules imbedded in the device was observed to exhibit diverse time- and electrical bias-dependent effects. These include: (i) fluorescence quenching due to interactions between MEH-PPV and holes in the TPD hole-transport layer; (ii) fluorescence quenching, or "photobleaching", due to chemical defects at MEH-PPV generated by photooxidation; and (iii) a novel process, reductive "repair" of the oxidative chemical defects by externally injected carriers. These results demonstrate a very different mechanism for photobleaching of organic conjugated materials than is generally assumed to operate and, furthermore, suggest an intimate relationship among photobleaching, charge transport, and persistent photoconductivity in organic materials.     

High-pressure NMR study of water exchange on magnetic resonance imaging contrast agents

Abstract

The knowledge of water exchange reaction mechanism in aqueous solutions of Gd³⁺ polyaminocarboxylates is important for the understanding of the relatively slow water exchange rates measured for these complexes. Variable ressure measurements show a change of mechanism from associatively activated on [Gd(H₂O)₈]³⁺ and [Gd(PDTA)(H₂O₂)₂]^? to probably limiting dissociative on the MRI contrast agents [Gd(DOTA)(H₂O)]^?, [Gd(DTPA)(H₂O)]^2? and [Gd(DTPA-BMA)(H₂O)].     

Enhancing signal-to-noise ratio and resolution in low-field NMR relaxation measurements using post-acquisition digital filters

The traditional way to enhance signal-to-noise ratio (SNR) of nuclear magnetic resonance (NMR) signals is to increase the number of scans. However, this procedure increases the measuring time that can be prohibitive for some applications. Therefore, we have tested the use of several post-acquisition digital filters to enhance SNR up to one order of magnitude in time domain NMR (TD-NMR) relaxation measurements. The procedures were studied using continuous wave free precession (CWFP-T₁) signals, acquired with very low flip angles that contain six times more noise than the Carr–Purcell–Meiboom–Gill (CPMG) signal of the same sample and experimental time. Linear (LI) and logarithmic (LO) data compression, low-pass infinity impulse response (LP), Savitzky–Golay (SG), and wavelet transform (WA) post-acquisition filters enhanced the SNR of the CWFP-T₁ signals by at least six times. The best filters were LO, SG, and WA that have high enhancement in SNR without significant distortions in the ILT relaxation distribution data. Therefore, it was demonstrated that these post-acquisition digital filters could be a useful way to denoise CWFP-T₁, as well as CPMG noisy signals, and consequently reducing the experimental time. It was also demonstrated that filtered CWFP-T₁ method has the potential to be a rapid and nondestructive method to measure fat content in beef and certainly in other meat samples.     

Etorphine‐Related Ferrocenyl‐Substituted Morphinan Alkaloids

The two diastereoisomeric ferrocenyl‐substituted orvinols 2 and 3 were prepared. The modified alkaloids are still able to interact with opioid receptors (see Table). The ferrocene moiety allows highly selective and sensitive electrochemical detection. The X‐ray crystal structure of the major isomer 2 was determined. The combination of a metallocene and a morphinan alkaloid holds promise for useful antitumor activity.     

Was wissen Calamari über Sarin? Enzymatische Dekontamination von Nervenkampfstoffen

Together with detection and use of protective clothing, decontamination is the third important part in NBC defence and NBC protection. Enzymes play an important role in the research field of new and environmentally friendly decontaminants. In 1946, organophosphate cleaving enzymes were first mentioned, and in the next decades further enzymes (i.e., DFPase) against G‐type nerve agents were discovered. After the cloning of the DFPase gene sequence in the 90s, the potential of DFPase as an environmentally friendly decontaminant was shown. In technical decontamination experiments, it was shown that the conditions for an enzyme‐based decontamination concept could be met for one class of chemical agents. However, the success of a general enzyme decontamination concept depends on the discovery of new enzymes against other classes of chemical agents, i.e., mustard and VX.     

Improvement and simplification of synthesis of 3-aryloxy-1,2-epoxypropanes using solvent-free conditions and microwave irradiations. Relation with medium effects and reaction mechanism

Some 3-aryloxy-1,2-epoxypropanes, interesting as potential synthons in β-adrenergic receptor antagonists preparation, were obtained in excellent yields (65-96% within 2-17 min) by microwave activation (monomode system) using solid-liquid solvent-free phase transfer catalysis (PTC). The best results for the O-alkylation of some phenols with epichlorohydrin were obtained using TBAB and NaOH/K₂CO₃ (1:4 mol/mol) as phase transfer catalyst and more acceptable basic system, respectively. These new procedure is compared with classical methods. Significant specific microwave effect (non-purely thermal) was evidenced in all cases. They were discussed in terms of reaction medium and mechanism, taking into account the variations in polarity of the systems.