Lactones phenoliques halomethylees,inhibiteurs bifonctionnels de proteases—II : Preparation de derives halomethyles de la dihydro-3,4 coumarine et de la benzofuranone-2

o-Hydroxy phenyl propionic and o-hydroxy phenyl acetic acids give mixtures of ortho- and para-hydroxymethylated phenolic acid sodium salts which with thionyl chloride undergo benzylic chlorination and lactonisation; para- and ortho-chloromethylated derivatives of 3,4-dihydrocoumarin and of benzofuran-2-one are thus obtained in two steps. The bromomethylation of (nitro-3 hydroxy-2 phenyl) and (nitro-5 hydroxy-2 phenyl) propionic acids yields 3,4-dihydro-8-nitro-6-bromomethyl- and 3,4-dihydro-6-nitro-8-bromomethyl-coumarins. Some radioactive derivatives have also been synthesised.     

Infrared dichroism of glassy polycarbonate at small strains

The dichroism of the 889, 1364, and 3063 cm^?1 infrared absorption bands of glassy, amorphous polycarbonate has been measured as a function of the strain in the range 0 to 2% at 23°C. The data obtained for these three bands superpose rather well over this strain range. Negligible dichroism is observed up to about 0.6% strain; above this level, the dichroic ratio increases in an approximately linear manner. Independent mechanical data, obtained under comparable conditions of time-scale and temperature, are cited which show that a transition from approximately linear to marked non-linear viscoelastic behavior occurs with glassy polycarbonate in the range 0.7 to 1.0% strain. The coincidence on the strain axis of a relatively abrupt increase in optical absorption anisotropy with a distinct change in Young's modulus is discussed in terms of a recent molecular theory of deformation of glassy polymers. It is suggested that the data are consistent with the view that the transition from linear to nonlinear viscoelastic behavior in glassy polycarbonate is marked by the onset of significant rotation around backbone bonds.     

Azobenzene-containing monolayer with photoswitchable wettability

A compact monolayer containing azobenzene has been prepared on silicon substrates. The elaboration route consisted of covalent grafting of freshly synthesized azobenzene moieties onto an isocyanate-functionalized self-assembled monolayer (SAM). The highly packed and ordered isocyanate-functionalized SAM and the azobenzene-functionalized SAM were monitored and characterized by contact angle measurements and X-ray reflectivity (XR). Photoswitching of the wettability of the film induced by the reversible cis-trans isomerization of the azobenzene chromophores is experimentally shown from water and olive oil contact angle measurements.     

Identification of the estrogen receptor Cd-binding sites by chemical modification

The widely reported interactions of the estrogen receptor (ER) with endocrine disrupting chemicals (EDCs) present in the environment gave raise to public concern and led to a number of screening and testing initiatives on the international level. Recent studies indicated that certain heavy metals, including cadmium, can mimic the effects of the endogenous estrogen receptor agonist 17beta-estradiol, and lead to estrogen receptor activation. Previous studies of the chimeric proteins, which incorporate the ligand-binding domain of the human ER, identified Cys 381, Cys 447, Glu 523, His 524 and Asp 538 as possible sites of interactions with cadmium. In the present study we utilized the rainbow trout ER ligand-binding domain fused to glutathione-S-transferase, and used Cd-shielding against various types of chemical modification of the fusion protein to study non-covalent interactions between the ER and Cd. The distribution of exposed and shielded residues allowed to identify amino acid residues involved in the interaction. Our data indicated preferential protection of Cys groups by cadmium, suggesting their involvement in the interaction. This supports data found in the literature on the strong binding affinity of the thiol group towards metals. However, not all Cys in the fusion protein sequence were protected against chemical modification, illustrating the importance of their chemical environment. In general, the location of rtER-LBD Cys residues implicated in Cd interactions did not confirm assignments made by alanine-scanning mutagenesis for the hER, probably due to differences in experimental setup and fusion proteins used. The involvement of other functional groups such as carboxylic acids in the Cd interactions, though not confirmed, can not be completely ruled out due to the general limitations of the chemical modification approach discussed in detail. Suggestions for an improved experimental setup were made.     

Evidence for B0 s-->phiphi decay and measurements of branching ratio and A(CP) for B+ -->phiK+

We present the first evidence of charmless decays of the B(0)(s) meson, the decay B(0)(s)--> phiphi, and a measurement of the branching ratio BR(B(0)(s)--> phiphi) using 180 pb(-1) of data collected by the CDF II experiment at the Fermilab Tevatron collider. In addition, the BR and direct CP asymmetry for the B+-->phiK+ decay are measured. We obtain BR(B(0)(s)--> phiphi)=[14(+6)(-5)(stat)+/-6(syst)] x 10(-6), BR(B+-->phiK+)=[7.6+/-1.3(stat)+/-0.6(syst)] x 10(-6), and A(CP)(B+-->phiK+)= -0.07+/-0.17(stat)+0.03 / -0.02(syst). Both decays are governed in the standard model by second order (penguin) b-->s(-)ss amplitudes.     

Measurement of the cross section for prompt diphoton production in pp collisions at square root of s=1.96 TeV

We report a measurement of the rate of prompt diphoton production in pp collisions at square root of s=1.96 TeV using a data sample of 207 pb(-1) collected with the upgraded Collider Detector at Fermilab. The background from nonprompt sources is determined using a statistical method based on differences in the electromagnetic showers. The cross section is measured as a function of the diphoton mass, the transverse momentum of the diphoton system, and the azimuthal angle between the two photons and is found to be consistent with perturbative QCD predictions.