Search for the CP-violating decays Upsilon(4S)-->B0B0-->J/psiKS0+J/psi(etac)KS0

We report the first search for CP-violating decays of the Upsilon(4S) using a data sample that contains 535 x 10(6) Upsilon(4S) mesons with the Belle detector at the KEKB asymmetric-energy e(+)e(-) collider. A partial reconstruction technique is employed to enhance the signal sensitivity. No significant signals were observed. We obtain an upper limit of 4 x 10(-7) at the 90% confidence level for the branching fractions of the CP violating modes, Upsilon(4S)-->B(0)B(0)-->J/psiK(S)(0)+J/psi(eta(c))K(S)(0). Extrapolating the result, we find that an observation with 5sigma significance is expected with a 30 ab(-1) data sample, which is within the reach of a future super B factory.     

Search for B --> h(*)nunu[over ] decays at Belle

We present a search for the rare decays B --> h(*)nunu[over ], where h(*) stands for a light meson. A data sample of 535 x 10{6} BB[over ] pairs collected with the Belle detector at the KEKB e{+}e{-} collider is used. Signal candidates are required to have an accompanying B meson fully reconstructed in a hadronic mode and signal side particles consistent with a single h(*) meson. No significant signal is observed and we set upper limits on the branching fractions at 90% confidence level. The limits on B{0} --> K{*0}nunu[over ] and B{+} --> K{+}nunu[over ] decays are more stringent than the previous constraints, while the first searches for B{0} --> K{0}nunu[over ], pi{0}nunu[over ], rho{0}nunu[over ], varphinunu[over ] and B{+} --> K{*+}nunu[over ], rho{+}nunu[over ] are reported.     

Measurement of CP asymmetry in a time-dependent Dalitz analysis of B0-->(rhopi)0 and a constraint on the quark mixing matrix angle phi2

We present a measurement of CP asymmetry using a time-dependent Dalitz plot analysis of B0-->pi+pi-pi0 decays based on a 414 fb(-1) data sample containing 449 x 10(6) BB pairs. The data was collected on the Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric energy e+ e- collider. Combining our analysis with information on charged B decay modes, we perform a full Dalitz and isospin analysis and obtain a constraint on the CKM angle phi2, 68 degrees < phi2 < 95 degrees as the 68.3% confidence interval for the phi2 solution consistent with the standard model (SM). A large SM-disfavored region also remains.     

Reflected shock tube studies of high-temperature rate constants for OH + C2H2 and OH + C2H4

The reflected shock tube technique with multi-pass absorption spectrometric detection of OH-radicals at 308 nm (corresponding to a total path length of approximately 4.9 m) has been used to study the reactions, OH + C(2)H(2)--> products (1) and OH + C(2)H(4)--> C(2)H(3) + H(2)O (2). The present optical configuration gives a S/N ratio of approximately 1 at approximately 0.5-1.0 x 10(12) radicals cm(-3). Hence, kinetics experiments could be performed at [OH](0) = approximately 4-20 ppm thereby minimizing secondary reactions. OH was produced rapidly from the dissociations of either CH(3)OH or NH(2)OH (hydroxylamine). A mechanism was then used to obtain profile fits that agreed with the experiment to within <+/-5%. The derived Arrhenius expressions, in units of cm(3) molecule(-1) s(-1) are: k(1) = (1.03 +/- 0.24) x 10(-10) exp(-7212 +/- 417 K/T) for 1509-2362 K and k(2) = (10.2 +/- 5.8) x 10(-10) exp(-7411 +/- 871 K/T) for 1463-1931 K. The present study is the first ever direct measurement for reaction (1) at temperatures >1275 K while the present results extend the temperature range for (2) by approximately 700 K. These values are compared with earlier determinations and with recent theoretical calculations. The calculations agree with the present data for both reactions to within +/-10% over the entire T-range.     

Reflected shock tube and theoretical studies of high-temperature rate constants for OH+CF3H<-->CF3+H2O and CF3+OH-->products

The reflected shock tube technique with multipass absorption spectrometric detection of OH radicals at 308 nm, using either 36 or 60 optical passes corresponding to total path lengths of 3.25 or 5.25 m, respectively, has been used to study the bimolecular reactions, OH+CF3H-->CF3+H2O (1) and CF3+H2O-->OH+CF3H (-1), between 995 and 1663 K. During the course of the study, estimates of rate constants for CF3+OH-->products (2) could also be determined. Experiments on reaction -1 were transformed through equilibrium constants to k1, giving the Arrhenius expression k1=(9.7+/-2.1)x10(-12) exp(-4398+/-275K/T) cm3 molecule(-1) s(-1). Over the temperature range, 1318-1663 K, the results for reaction 2 were constant at k2=(1.5+/-0.4)x10(-11) cm3 molecule(-1) s(-1). Reactions 1 and -1 were also studied with variational transition state theory (VTST) employing QCISD(T) properties for the transition state. These a priori VTST predictions were in good agreement with the present experimental results but were too low at the lower temperatures of earlier experiments, suggesting that either the barrier height was overestimated by about 1.3 kcal/mol or that the effect of tunneling was greatly underestimated. The present experimental results have been combined with the most accurate earlier studies to derive an evaluation over the extended temperature range of 252-1663 K. The three parameter expression k1=2.08x10(-17) T1.5513 exp(-1848 K/T) cm3 molecule(-1) s(-1) describes the rate behavior over this temperature range. Alternatively, the expression k1,th=1.78x10(-23) T3.406 exp(-837 K/T) cm3 molecule(-1) s(-1) obtained from empirically adjusted VTST calculations over the 250-2250 K range agrees with the experimental evaluation to within a factor of 1.6. Reaction 2 was also studied with direct CASPT2 variable reaction coordinate transition state theory. The resulting predictions for the capture rate are found to be in good agreement with the mean of the experimental results and can be represented by the expression k2,th=2.42x10(-11) T-0.0650 exp(134 K/T) cm3 molecule(-1) s(-1) over the 200-2500 K temperature range. The products of this reaction are predicted to be CF2O+HF.     

Chemically triggered C-ON bond homolysis of alkoxyamines. Quaternization of the alkyl fragment

The C-ON bond homolysis in alkoxyamine 2a can be chemically triggered by the protonation of the 4-pyridylalkyl fragment. The resulting 15-fold increase in k(d) (Chem. Commun. 2011, 47, 4291-4293) was investigated experimentally and theoretically by quaternization of the pyridyl moiety using methylating (MeOTs), acylating (AcCl), and benzylating (PhCH(2)Br) agents as well as by oxidation of the pyridyl moiety into N-oxide and by the formation of a dative bond with BH(3) as a Lewis acid.     

Dynamic structure mediated by graphitelike Al nets on the Al2Cu (001) surface

A detailed study of the (001) surface of the Al(2)Cu crystal using both experimental and ab initio computational methods is presented in this work. The combination of both approaches gives many arguments to match the surface plane with a bulk truncated surface model terminated by incomplete Al planes. The missing rows of Al atoms lead to a 2√2×√2R 45° surface reconstruction with two domains rotated by 90° from each other. Ab initio calculations demonstrate that the energetic cost associated with the removal of pairs of Al atoms is the lowest for the two nearest surface Al atoms (covalentlike interaction). They reveal that the remaining atomic rows of various widths are oriented according to the graphitelike Al 6(3) nets used to describe the Al(2)Cu bulk structure. The surface dynamics observed at 300 K at the Al(2)Cu surface is also presented. Finally, configurational and vibrational entropies are introduced to discuss the reduced surface plane density.     

An Improved Reduction Procedure in the Synthesis of Substituted Pyrrolidines via An Aminomercuration/Reduction Sequence of Primary Alkenylamines

Aminomercuration/reduction sequence of δ-alkenylamines is a typical route to substituted pyrrolidines. Backward reaction to the starting material is a major drawback which occurs during sodium borohydride reduction of the intermediate organomercurial. We describe here a new reduction procedure which prevents almost completely this backward reaction and leads to significant increases in the yields of pyrrolidines.     

Filtrage linéaire par morceaux avec petit bruit d'observation

We consider a piecewise linear filtering problem with small observation noise. In two different situations we construct an approximate finite-dimensional filter based on several Kalman-Bucy filters running in parallel and a procedure of tests. In the first case our work generalizes some results of Fleminget al. to more general piecewise linear dynamics.

     

Dynamical structure factor and spin-density separation for a weakly interacting two-component Bose gas

We show that spin-density separation in a Bose gas is not restricted to 1D but also occurs in higher dimensions. The ratio (alpha) of the intraspecies atom-atom interaction strength to the interspecies interaction strength strongly influences the dynamics of spin-density separation and the elementary excitations. The density wave is phononlike for all values of alpha. For alpha < 1, the spin wave is also phononlike. The spin waves have a quadratic dispersion in the alpha=1 coupling regime, while in the phase separated regime (alpha > 1) the spin waves are found to be damped. The dynamical structure factor reveals two distinct peaks corresponding to the density and spin waves for alpha < or =1. For alpha > 1 there is only one dynamical structure factor peak corresponding to the density wave.