Relativistic corrections to the electric polarizability of compound systems

The widely used relation alpha; = alpha(0)+Deltaalpha for the electric polarizability, where Deltaalpha is proportional to the r.m.s. charge radius of the system, is revisited within a simple model of two spinless particles bound electromagnetically. A complete set of the relativistic corrections to alpha(0) following from the Breit Hamiltonian is obtained. It is shown that these corrections modify the result for alpha; in comparison to that obtained with alpha(0) taken in the nonrelativistic approximation. We propose that the same situation can take place in the more complicated case of hadrons. Special attention is devoted to the correct definition of the center-of-mass coordinates which are found to be very important.     

Magnetoresistance anisotropy in Si /SiGe in tilted magnetic fields: experimental evidence for a stripe-phase formation

We observe pronounced transport anisotropies in magnetotransport experiments performed in the two-dimensional electron system of a Si/SiGe heterostructure. They occur when an in-plane field is used to tune two Landau levels with opposite spin to energetic coincidence. The observed anisotropies disappear drastically for temperatures above 1 K. We propose that our experimental findings may be caused by the formation of a unidirectional stripe phase oriented perpendicular to the in-plane field.     

Prospects for the measurement of the structure of the coupling of a Higgs boson to weak gauge bosons in weak boson fusion with the ATLAS detector

The prospects for the measurement of the tensor structure of the vertex between a standard model Higgs boson and two weak gauge bosons using the distribution of the azimuthal angles between the two tagging jets in the weak boson fusion channel are studied in a Monte Carlo analysis using the fast simulation of the ATLAS detector. The decay channels H→τ⁺τ^-→ll+4ν, H→τ⁺τ^-→lh+3ν at m_H=120 GeV and H→W⁺W^-→llνν at m_H=160 GeV are used in the analysis. For a standard model Higgs boson it is found that purely anomalous couplings are expected to be excluded at a confidence level corresponding to 2σ or more at m_H=120 GeV and more than 5σ at m_H=160 GeV from 30 fb^-1 of data. With a value of 1 roughly reproducing the standard model cross section for a purely anomalous coupling, the standard deviation in a measurement of a contribution of a CP even anomalous coupling in addition to the standard model coupling is estimated to be 0.20 at m_H=120 GeV and 0.09 at m_H=160 GeV.     

Properties of the πη,$ \eta{^\prime}$,σ, f0(980) and a0(980) mesons and their relevance for the polarizabilities of the nucleon

The signs and values of the two-photon couplings F _Mγγ of mesons (M) and their couplings g_MNN to the nucleon as entering into the t -channel parts of the difference of the electromagnetic polarizabilities (α - β) and the backward angle spin polarizabilities γ_π are determined. The excellent agreement achieved with the experimental polarizabilities of the proton makes it possible to make reliable predictions for the neutron. The results obtained are α_n = 13.4±1.0 , β_n = 1.8±1.0 (10^-4fm^3), and γ⁽ⁿ⁾ _π = 57.6±1.8 (10^-4fm^4). New empirical information on the flavor wave functions of the f ₀(980) - and the a ₀(980) -meson is obtained.     

Precision synthesis of microstructures in star‐shaped copolymers of ϵ‐caprolactone,L‐lactide,and 1,5‐dioxepan‐2‐one

Star‐shaped homo‐ and copolymers were synthesized in a controlled fashion using two different initiating systems. Homopolymers of ε‐caprolactone, L ‐lactide, and 1,5‐dioxepan‐2‐one were firstly polymerized using (I) a spirocyclic tin initiator and (II) stannous octoate (cocatalyst) together with pentaerythritol ethoxylate 15/4 EO/OH (coinitiator), to give polymers with identical core moieties. Our gained understanding of the versatile and controllable initiator systems kinetics, the transesterification reactions occurring, and the role which the reaction conditions play on the material outcome, made it possible to tailor the copolymer microstructure. Two strategies were used to successfully synthesize copolymers of different microstructures with the two initiator systems, i.e., a more multiblock‐ or a block‐structure. The correct choice of the monomer addition order enabled two distinct blocks to be created for the copolymers of poly(DXO‐co‐LLA) and poly(CL‐co‐LLA). In the case of poly(CL‐co‐DXO), multiblock copolymers were created using both systems whereas longer blocks were created with the spirocyclic tin initiator. © 2008 Wiley Periodicals, Inc. JPolym Sci Part A: Polym Chem 46: 1249–1264, 2008     

Characterization of dielectric barrier electrospray ionization for mass spectrometric detection

A novel electrospray interface is presented which induces an electric field by dielectric polarization through a non-conductive barrier. Therefore, a square-wave high-voltage signal is applied. This technique allows mass spectrometric measurements in the positive as well as in the negative mass spectrometry mode without changing the polarity of the potential applied, and it decreases the risk of undesired discharges, induced by high electric currents. The applicability of this technique is demonstrated by mass spectrometric determination of reserpine.     

Synthesis of core‐shell structured carboxylated microparticles with a straightforward procedure and their evaluation as a polymer support

Poly(trimethylolpropane trimethacrylate) microspheres with a narrow size distribution were obtained by precipitation polymerization. They were subsequently modified by surface grafting with acrylic acid in a polar ethanol–water reaction medium, without stabilizer, yielding core‐shell particles with diameters in the micrometer range. The resulting polymeric material was characterized by SEM and potentiometric titration, FTIR spectroscopy, and thermal analysis. It was shown that the particle characteristics (size, size distribution, and functionality) obtained by this straightforward procedure can be controlled by modifying the synthesis parameters (monomer concentration, agitation rate, and temperature). The high functionality, the chemical and physico‐mechanical stability, as well as the possibility to control the performances of the resulting polymeric materials by synthesis allow its applications in various areas. Envisaging separation and catalysis domains, Cu(II), Cd(II), and Cr(III) uptake capacity from aqueous solutions was investigated under noncompetitive conditions as a function of synthesized particle functionality, time, and pH range. It was also found that the addition of the carboxylated microparticles to polyethylene stabilized with α‐tocopherol improved the thermo‐oxidative behaviour of the polymeric material. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5889–5898, 2005     

Use of ion mobility mass spectrometry and a collision cross‐section algorithm to study an organometallic ruthenium anticancer complex and its adducts with a DNA oligonucleotide

We report the development of an enhanced algorithm for the calculation of collision cross‐sections in combination with Travelling‐Wave ion mobility mass spectrometry technology and its optimisation and evaluation through the analysis of an organoruthenium anticancer complex [(η⁶‐biphenyl)Ru^II(en)Cl]⁺. Excellent agreement was obtained between the experimentally determined and theoretically determined collision cross‐sections of the complex and its major product ion formed via collision‐induced dissociation. Collision cross‐sections were also experimentally determined for adducts of this ruthenium complex with the single‐stranded oligonucleotide hexamer d(CACGTG). Ion mobility tandem mass spectrometry measurements have allowed the binding sites for ruthenium on the oligonucleotide to be determined. Copyright © 2009 John Wiley & Sons, Ltd.     

One-pot synthesis of tripodal tris(2-aminoethyl)amine derivatives from seven molecular components

Complex tripodal tris(2-aminoethyl)amine (tren)-based ligands have been prepared in a single-pot reaction of tren with 3 equiv each of cyclohexenone and a benzaldehyde derivative (i.e., from seven components and three molecular types). The highest yield of product was obtained for p-nitrobenzaldehyde, the most electrophilic aldehyde used.