Chiral morphologies and interfacial electronic structure of naphtho[2,3-a]pyrene on Au(111)

The adsorption of the two-dimensionally chiral naphtho[2,3-a]pyrene molecule has been studied on Au(111). Both structural and electronic properties of the naphtho[2,3-a]pyrene (NP)/Au(111) interface have been measured. Ultraviolet and X-ray photoelectron spectroscopy have been employed to measure the energies of the molecular orbitals of the NP film with respect to the gold Fermi level. A Schottky junction with a large interface dipole (0.99 eV) is formed between Au(111) and NP. Temperature-programmed desorption was used to determine that adsorbed NP has a binding energy of 102.2 kJ/mol. Chiral domains have been observed with scanning tunneling microscopy due to the spontaneous phase separation of the 2-D enantiomers. Two distinct structural polymorphs have been observed, one of which has homochiral paired molecular rows. Models of the 2D structure are proposed that are in excellent agreement with experimental measurements.     

FLUORESCENCE DECAY KINETICS and CHARACTERISTICS OF BIMOLECULAR EXCITON ANNIHILATION IN CHLOROPLASTS

Abstract— The decay profiles of the fluorescence of dark-adapted spinach chloroplasts (0^A°C) excited with single 30 ps 532 nm laser pulses of varying intensities were measured with a low-jitter streak camera system. By comparing the decay profiles of the fluorescence at low and high laser fluences, i.e. in the absence and presence, respectively, of dynamic bimolecular exciton-exciton annihilation effects, the duration of such dynamic annihilation events can be estimated. A simple model suggests that the influence of bimolecular annihilation events on the fluorescence decay kinetics should disappear within a time interval corresponding to the low intensity, unimolecular lifetime of the exciton population which is subject to exciton-exciton annihilation. The low intensity fluorescence decay profiles are characterized by three to four lifetimes (Reviewed by A. R. Holzwarth, Photochem. Photobiol. 43,707–725, 1986); it is shown here that only the shortest fluorescence components are subject to exciton annihilation, since the kinetics of the fluorescence decay are influenced by annihilations only within the initial 150–200 ps time interval after the excitation pulse. The amplitudes (but not the decay kinetics) of the longer-lived fluorescence components are decreased at high levels of laser pulse excitations, suggesting that these components are derived from the shorter-lived fluorescence decay components. The implications of these results are*discussed within the contexts of current models of the fluorescence in chloroplasts.     

Selective electrochemical glycosylation by reactivity tuning

Electrochemical glycosylation of a selenoglycoside donor proceeds efficiently in an undivided cell in acetonitrile to yield beta-glycosides. Measurement of cyclic voltammograms for a selection of seleno-, thio-, and O-glycosides indicates the dependence of oxidation potential on the anomeric substituent allowing the possibility for the rapid construction of oligosaccharides by selective electrochemical activation utilising variable cell potentials in combination with reactivity tuning of the glycosyl donor. A variety of disaccharides are readily synthesised in high yield, but limitations of the use of selenoglycosides as glycosyl donors for selective glycosylation of thioglycoside acceptors are exposed. The first electrochemical trisaccharide synthesis is described.     

Multicomponent glass optical fibres with a lowered water content and reduced loss

A technique has been developed to reduce the ?OH content of multicomponent glasses. The glasses were treated with perfluoropropane and the linear absorption coefficient of ?OH reduced from typically 0.08 to as low as 0.01 cm^?1, which corresponds to a reduction of ?OH content to approximately 2 ppm. A fibre pulled from treated glasses had a reduced loss at 1.3 μm, and a loss of 2.9 dB km^?1 at 1.12 μm which is the lowest reported loss for a fibre prepared by a double crucible technique.     

Characterization of the surface of­bulk‐molded compounds

The automotive industry more and more frequently uses composite materials such as molded compounds (sheet‐molded compounds, SMC, or bulk‐molded compounds, BMC). Bonding is then the only way of assembling two pieces. Consequently, and in order tentatively to predict the adhesive behavior of such materials, it is necessary to have a good knowledge of their surface properties. Here, different complementary techniques of surface analysis allowed us, on the one hand, to reach this aim for BMCs prepared by compression molding and, on the other hand, to show the influence on the surface properties of the concentration and composition of the internal release agent added to the blend. The surface heterogeneity and the organic nature of the surface of the compounds are shown and no phase separation occurs there as in the bulk. Mold release agents remain in the surface layer and induce some acid–base character to the surface material which depends on the type of stearate introduced in the blend. Copyright © 1999 John Wiley & Sons, Ltd.     

Experimental investigation of subcooled flow boiling of a 50/50 ethylene glycol/water mixture in finned rectangular aluminum channels

Subcooled flow boiling heat transfer experiments were performed with a 50/50 ethylene glycol/water mixture in a finned aluminum channel. The channel represented a hybrid electric vehicle power electronic cold plate receiving a 50/50 mixture from the radiator at 105°C and 2 atmospheres. Experiments used a range of mixture flow rates and both top- and bottom-heating situations. Boiling curves were generated, and subcooled flow boiling heat transfer coefficients were determined including the test channel fin effects. Subcooled flow boiling heat transfer coefficients showed a 25–30% increase compared to single-phase convection.     

Discovery of doubly magic 48Ni

In an experiment at the SISSI/LISE3 facility of GANIL, we used the projectile fragmentation of a primary 58Ni26+ beam at 74.5 MeV/nucleon with an average current of 3 &mgr;A on a natural nickel target to produce very neutron-deficient isotopes. In a 10-day experiment, 287 42Cr isotopes, 53 45Fe isotopes, 106 49Ni isotopes, and 4 48Ni isotopes were unambiguously identified. The doubly magic nucleus 48Ni, observed for the first time, is the most proton-rich isotope ever identified with an isospin projection T(z) = -4. It is probably the last doubly magic nucleus with "classical" shell closures accessible for present-day facilities. Its observation allows us to deduce a lower limit for the half-life of 48Ni of 0.5 &mgr;s.     

Drawing induced absorption loss in multicomponent glass fibres

A drawing induced loss has been found to exist in multicomponent glass optical fibres, and has been shown to be due to absorption. Two loss peaks were identified at 580 and 360 nm with peak heights of 340 and 490 dBkm^?1, respectively. The 580 nm peak was believed to be due to silicon oxygen hole centres formed during fibre drawing. The induced loss could be partially removed by annealing, and the behaviour of the induced loss under various heat treatments was investigated. It was also found that the loss could be completely eliminated by the addition of 0.1 wt% As₂O₃ to the glass melt.     

Bifunctional asymmetric catalysis: a tandem nucleophile/Lewis acid promoted synthesis of beta-lactams

[reaction: see text]. We describe a superior procedure for the catalytic, asymmetric synthesis of beta-lactams using a bifunctional catalyst system consisting of a chiral nucleophile and an achiral Lewis acid.