Synthese de composes aromatiques comportant les groupements ocf2br et scf2brI - Action du dibromodifluoronéthane sur les thiophénate et phénate de potassium

The synthesis of, C₆H₅OCF42Br and C₆H₅SCF₂Br from CF₂Br₂ is discribed.     

The reduction of Ag+ in metallic silver on pseudomelanin films allows for antibacterial activity but does not imply unpaired electrons

Dopamine-melanin films produced through the oxidation of dopamine in the presence of oxygen as an oxidant allow to reduce silver ions onto silver particles as already described in the paper by Lee et al. (H. Lee, S.M. Dellatore, W.M. Miller, P.B. Messersmith, Science 318 (2007) 426.). This reduction process has to occur through the oxidation of moieties present in the melanin film. This investigation shows that the free radicals present in the pseudomelanin film, quantified by means of electron spin resonance spectroscopy (ESR) for the first time, are not used in the transformation of Ag(+) cations to deposit silver. The ESR signal is hardly affected by the deposition of silver particles. On the other hand, X-ray photoelectron spectroscopy shows a small increase in the density of quinone groups and a small decrease of catechol groups on the surface of the film during the deposition of silver. This suggests that the deposited pseudomelanin films contain a significant fraction of catechol groups able to trigger reduction processes of metallic cations. These silver nanoparticles remain adherent to the melanin films and allow for a quantitative killing of Escherichia coli over a broad range of bacterial dilutions. However, the presence of the bacteria induces a release of the nanoparticles. The pseudomelanin films cannot be reused again for a silver ion reduction step. Nevertheless, the easy preparation of the pseudomelanin-silver composite and its effective one shot bacterial killing activity renders the strategy presented in this paper attractive. Some fundamental questions about redox process allowed by the pseudomelanin films will also be asked.     

Phase correction-based singularity function analysis for partial k-space reconstruction

Partial k-space acquisition is a conventional method in magnetic resonance imaging (MRI) for reducing imaging time while maintaining image quality. In this field, image reconstruction from partial k-space is a key issue. This paper proposes an approach fundamentally different from traditional techniques for reconstructing magnetic resonance (MR) images from partial k-space. It uses a so-called singularity function analysis (SFA) model based on phase correction. With such a reconstruction approach, some nonacquired negative spatial frequencies are first recovered by means of phase correction and Hermitian symmetry property, and then the other nonacquired negative and/or positive spatial frequencies are estimated using the mathematical SFA model. The method is particularly suitable for asymmetrical partial k-space acquisition owing to its ability of overcoming reconstruction limitations due to k-space truncations. The performance of this approach is evaluated using both simulated and real MR brain images, and compared with existing techniques. The results demonstrate that the proposed SFA based on phase correction achieves higher image quality than the initial SFA or the projection-onto-convex sets (POCS) method.     

Convenient method for the rapid generation of highly active and enantioselective yttrium catalysts for asymmetric hydroamination

A facile method for the preparation of highly active and enantioselective yttrium precatalysts for asymmetric hydroamination of gem-disubstituted aminoalkenes, from the combination of YCl(3) or YCl(3)(THF)(3.5) with ligand (R)- and n-BuLi is described.     

Towards zirconium phosphonate-based microarrays for probing DNA-protein interactions: critical influence of the location of the probe anchoring groups

Terminal phosphate groups on double-stranded DNA probes bind strongly to glass substrates coated with a zirconium phosphonate monolayer, and probes immobilized in this way as microarrays can be used to detect protein targets. The sensitivity of the microarray was shown to be enhanced by the use of a polyguanine segment ((G)n , n > or = 5) as a spacer between the phosphate linker and the protein interaction domain. More importantly, the presence of phosphate linkers on both ends of the dsDNA probes leads to significant enhancement of target capture. The relevant characteristics of the different probes when bound to the surface were determined, by the original use of a combination of surface characterization techniques (XPS, AFM, and Sarfus). In this context, the location of the phosphate linkers in the duplex probes was found to result in different probe surface coverage and presentation on the surface, which affect subsequent interactions with the target protein.