Search for the Hypothetical pi -> mu x Decay

The KARMEN collaboration has reported the possible observation of a hitherto unknown neutral and weakly interacting particle x, which is produced in the decay pi -> mu + x with a mass m(x) = 33.9 MeV. We have searched for this hypothetical decay branch by studying muons from pion decay in flight with the LEPS spectrometer at the piE3 channel at PSI and find branching ratios BR(pi- to mu- anti-x) < 4e-7 and BR(pi+ to mu+ x) < 7e-8 (95\% C.L.). Together with the limit BR > 2e-8 derived in a recent theoretical paper our result would leave only a narrow region for the existence of x if it is a heavy neutrino.Comment: 10 pages, TeX (uses epsf), 3 Postscript figures uu-encode

Superspace Description of the Crystal Structures of Can(Nb,Ti)nO3n+2Ca_{n}(Nb,Ti)_{n}O_{3n+2} (n = 5 and 6)

The crystal structures of two members of the homologous series Ca(n)(Nb,Ti)(n)O(3n + 2), with n = 5 and 6, are presented within the superspace formalism. A common (3 + 1)-dimensional superspace model is used to describe the crystal structures of both compositions within a particular homologous series, where the primary modulation wavevector and the width of the atomic domains vary systematically with composition. The two crystal structures are characterized as commensurately modulated structures consisting of discontinuous atomic domains described by occupational crenel functions. The displacive modulation functions for the two compounds exhibit similarities, but they also show that the idea of a unified superspace model does not extend toward the precise atomic positions. For n = 6, the centrosymmetric (3 + 1)-dimensional superspace symmetry provides a natural explanation for the pseudo-symmetries that are present in the non-centrosymmetric (three-dimensional) superstructure of this compound. The efficiency of the superspace approach is demonstrated by structure refinements in (3 + 1)-dimensional superspace and by comparing these results with the refinements in their three-dimensional superstructures

Singlet Fission in Weakly Interacting Acene Molecules

The energy conversion in solar cells has conventionally been limited by the Shockley-Queisser limit. Singlet fission (SF), a decay mechanism where a single excited singlet state is converted into two triplet states, can drastically improve this efficiency. For the most part, observation of SF has been limited to crystalline structures in solids and films, where strong ordering was present. Here we report on singlet fission in a disordered system where organic chromophores are distributed on the surface of a rare gas cluster. In this case, the intermolecular distances and degree of excitation can be varied to obtain their effects on the rate of singlet fission. We introduce a kinematic model that takes into account the details of the geometrical arrangement of the system as well as the time-dependent populations of the relevant states of each molecule and evaluate the trends obtained by SF on the experimental observables

Electron-Deficient and Polycenter Bonds in the High-Pressure γ−B28\mathrm{\gamma-B_{28}} Phase of Boron

The peculiar bonding situation in gamma boron is characterized on the basis of an experimental electron-density distribution which is obtained by multipole refinement against low-temperature single-crystal x-ray diffraction data. A topological analysis of the electron-density distribution reveals one-electron-two-center bonds connecting neighboring icosahedral B-12 clusters. A unique polar-covalent two-electron-three-center bond between a pair of atoms of an icosahedral cluster and one atom of the interstitial B-2 dumbbell explains the observed charge separation in this high-pressure high-temperature polymorph of boron

Novel bis(1,3,2-diazaphospholidine) ligands for asymmetric catalysis

A family of modularly designed chiral bis(1,3,2-diazaphospholidines) with N-aryl substituents (NP-PN) is reported. These compounds have been prepared in two steps from readily available (R,R)-1,2-diaminocyclohexane and tetrachlorodiphosphines. Examples in the set differ in the backbone and the aryl substituents, aiming at their application in asymmetric catalysis. Thus, [Rh(NBD)(NP-PN)]BF4 complexes lead to active catalysts in the hydrogenation of methyl α-acetamidoacrylate, which provide enantioselectivities up to 96% ee. In addition, NP-PN ligands also generate active catalysts in the hydroformylation of vinyl acetate, leading to high regioselectivities (iso:n ratio higher than 99:1) and enantioselectivities up to 65% ee. © 2013 American Chemical Society.Peer Reviewe