Observation of B+ --> K0K+ and B0 --> K0K0

We report observations of the b --> d penguin-dominated decays B+ --> K0K+ and B0 --> K0K0 in 316 fb(-1) of e+ e- collision data collected with the BABAR detector. We measure the branching fractions B(B+ --> K0K+) = (1.61+/-0.44+/-0.09) x 10(-6) and B(B0 --> K0K0 = (1.08+/-0.28+/-0.11) x 10(-6) and the CP-violating charge asymmetry A(CP)(K0K+) = 0.10+/-0.26+/-0.03. Using a vertexing technique previously employed in several analyses of all-neutral final states containing kaons, we report the first measurement of time-dependent CP-violating asymmetries in B0 --> K(S)0K(S)0, obtaining S = -1.28(-0.73-0.16)(+0.80+0.11) and C = -0.40+/-0.41+/-0.06. We also report improved measurements of the branching fraction B(B+ --> K0 pi+) = (23.9+/-1.1+/-1.0) x 10(-6) and CP-violating charge asymmetry A(CP)(K0 pi+) = -0.029+/-0.039+/-0.010.     

Spectroscopic characterization of a series of platinum acetylide complexes having a localized triplet exciton

In this work, we describe the spectroscopic properties of a series of platinum complexes containing one acetylide ligand per platinum, having the chemical formula trans-Pt(PBu(3))(2)((C[triple bond]CC(6)H(4))(n)()-H)Cl, n = 1-3 (designated as half-PEn-Pt) and compare their spectroscopic behavior with the well-characterized series trans-Pt(PBu(3))(2)((C[triple bond]CC(6)H(4))(n)-H)(2), n = 1-3 (designated as PEn-Pt). This comparison aims to determine if the triplet state of PEn-Pt is confined to one ligand or delocalized across the central platinum atom. We measured ground-state absorption spectra, fluorescence spectra, phosphorescence spectra, and triplet-state absorption spectra. The ground-state absorption spectra and fluorescence spectra both showed a blue shift when comparing half-PEn-Pt with PEn-Pt, showing the S(1) state is delocalized across the platinum. In contrast, the phosphorescence spectra of the two types of compounds had the same 0-0 band energy, showing the T(1) state was confined to one ligand in PEn-Pt. The triplet state absorption spectra blue shifted when comparing half-PEn-Pt with PEn-Pt, showing the T(n) state was delocalized across the central platinum. This comparison supports recently published work that suggested this confinement effect (Rogers, J. E et al. J. Chem. Phys. 2005, 122, 214701).     

On the approximability of the Simplified Partial Digest Problem

In this paper, we analyse the computational complexity of an optimization version of the Simplified Partial Digest Problem (SPDP), which is a mathematical model for DNA mapping based on the results of a simplified partial digest experiment. We prove that recognizing 46.16% of the elements of the DNA map in the error-free simplified partial digest experiment is NP-hard in the strong sense. This implies that the problem of maximizing the number of correct elements of the DNA map in the error-free simplified partial digest experiment is pseudopolynomially non-approximable with the approximation ratio .     

Open quantum dots: II. Probing the classical to quantum transition

Open quantum dots provide a natural system in which to study both classical and quantum features of transport. From the classical point of view these dots possess a mixed phase space which yields families of closed, regular orbits as well as an expansive sea of chaos. An important question concerns the manner in which these classical states evolve into the set of quantum states that populate the dot in the quantum limit. In the reverse direction, the manner in which the quantum states evolve to the classical world is governed strongly by Zurek's decoherence theory. This was discussed from the quantum perspective in an earlier review?(Ferry et?al 2011 Semicond. Sci. Technol. 26 043001). Here, we discuss the nature of the various classical states, how they are formed, how they progress to the quantum world, and the signatures that they create in magnetotransport and general conductance studies of these dots.     

A simulated annealing hyper-heuristic methodology for flexible decision support

Most of the current search techniques represent approaches that are largely adapted for specific search problems. There are many real-world scenarios where the development of such bespoke systems is entirely appropriate. However, there are other situations where it would be beneficial to have methodologies which are generally applicable to more problems. One of our motivating goals for investigating hyper-heuristic methodologies is to provide a more general search framework that can be easily and automatically employed on a broader range of problems than is currently possible. In this paper, we investigate a simulated annealing hyper-heuristic methodology which operates on a search space of heuristics and which employs a stochastic heuristic selection strategy and a short-term memory. The generality and performance of the proposed algorithm is demonstrated over a large number of benchmark datasets drawn from two very different and difficult problems, namely; course timetabling and bin packing. The contribution of this paper is to present a method which can be readily (and automatically) applied to different problems whilst still being able to produce results on benchmark problems which are competitive with bespoke human designed tailor made algorithms for those problems.     

Low-energy enhancement in the photon strength of 95Mo

A new experimental technique is presented using proton-γ-γ correlations from (94)Mo(d,p)(95)Mo reactions which allows for the model-independent extraction of the photon strength function at various excitation energies using primary γ-ray decay from the quasicontinuum to individual low-lying levels. Detected particle energies provide the entrance excitation energies into the residual nucleus while γ-ray transitions from low-lying levels specify the discrete states being fed. Results strongly support the existence of the previously reported low-energy enhancement in the photon strength function.     

In search of the plastic enzyme

Photozymes are novel polyelectrolytes made from mixtures of hydrophobic and hydrophilic comonomers. They often contain a relatively high concentration of bound chromophores as photon harvesting or antenna groups, which transport excitation energy to organic substrates located in the interior of the macromolecular coil in aqueous solution. Previous studies have shown that the photocatalytic behavior of these polymers has many similarities to natural enzymes which carry out thermal reactions in biological systems. Mechanistic studies of four photozyme reactions are discussed: (1) the oxidation of perylene to perylenequinones; (2) the dehalogenation of hexachloro- and pentachlorobenzene; (3) the high-yield synthesis of Vitamin D; and (4) the selective photolysis of aliphatic and aromatic ketones.