Coherent transport of neutral atoms in spin-dependent optical lattice potentials

We demonstrate the controlled coherent transport and splitting of atomic wave packets in spin-dependent optical lattice potentials. Such experiments open intriguing possibilities for quantum state engineering of many body states. After first preparing localized atomic wave functions in an optical lattice through a Mott insulating phase, we place each atom in a superposition of two internal spin states. Then state selective optical potentials are used to split the wave function of a single atom and transport the corresponding wave packets in two opposite directions. Coherence between the wave packets of an atom delocalized over up to seven lattice sites is demonstrated.     

High-spin states in the 96Tc nucleus

High-spin states in the ⁹⁶Tc nucleus have been studied with the reactions ⁸²Se(¹⁹F,5nγ) at 68 MeV and Zn(³⁶S,αpxn) at 130 MeV. Two γ-ray cascades (irregular bandlike structures) have been observed up to an excitation energy of about 10 MeV and spin 21-22?. Received: 19 January 2001 / Accepted: 30 March 2001     

Free-carrier absorption modulation in silicon nanocrystal slot waveguides

Free-carrier absorption (FCA) has proven to be an important obstacle in the development of a silicon-based laser; however, FCA may serve as a potential advantage in active silicon-based switches or modulators. In this work, we present FCA modulation in slot waveguides with silicon nanocrystals (Si-ncs) embedded in SiO(2) as the low-index slot material. Slot waveguides were fabricated with and without Si-ncs, and the presence of Si-ncs was shown to increase the pump-induced FCA loss in the waveguides by a factor of 4.5. We modeled the Si-nc material using a four-level rate equation analysis to estimate the excited population of Si-ncs, allowing us to extract a value of 2.6 × 10(-17) cm(2) for the FCA cross section of the Si-nc material.     

Preparation of hydrogels via ultrasonic polymerization

Several acrylic hydrogels were prepared via ultrasonic polymerization of water soluble monomers and macromonomers. Ultrasound was used to create initiating radicals in viscous aqueous monomer solutions using the additives glycerol, sorbitol or glucose in an open system at 37 °C. The water soluble additives were essential for the hydrogel production, glycerol being the most effective. Hydrogels were prepared from the monomers 2-hydroxyethyl methacrylate, poly(ethylene glycol) dimethacrylate, dextran methacrylate, acrylic acid/ethylene glycol dimethacrylate and acrylamide/bis-acrylamide. For example a 5% w/w solution of dextran methacrylate formed a hydrogel in 6.5 min in a 70% w/w solution of glycerol in water at 37° C with 20 kHz ultrasound, 56 W cm^?2. The ultrasonic polymerization method described here has a wide range of applications such a biomaterial synthesis where initiators are not desired.     

Material Discrimination in Nanoparticle Hetero-Aggregates by Analysis of Scanning Transmission Electron Microscopy Images

Hetero-contacts are interfaces between different materials at the nanoscale leading to novel functional properties. In hetero-aggregates, primary particles of at least two different materials are mixed at primary particle or cluster level. Double flame spray pyrolysis (DFSP) is a versatile technique for the controlled synthesis of such materials. Characterization of hetero-aggregates by scanning transmission electron microscopy (STEM) requires acquisition and evaluation of many aggregate images in order to derive statistically significant results. Usually, STEM energy dispersive X-ray spectroscopy (EDXS) is used to acquire elemental maps providing the material distribution of the primary particles within hetero-aggregates. However, the acquisition of a single EDXS map takes up to several minutes. For this reason, determination of material types of primary particles from the intensity in high-angle annular dark field STEM images alone is desirable. These images can be acquired within a couple of seconds. In the present work, a method is suggested which allows for achieving this objective. It can be applied to distinguish materials with a significant difference in their atomic number and hence sufficient material contrast in the STEM images.     

ORTHO-LITHIATION IN O-CARBONYL CHALCOGENIDES SYNTHESIS

Abstract

4,4-dimethyl 2-phenyl-2-oxazoline (or 2-thiazoline) and 4,4,6-trimethyl 2-phenyl-2-oxazine undergo regiospecific ortholithiation. The lithio intermediate reacts with chalcogenes (S, Se, Te) and methyliodide.     

Synthesis of Benzopyran Derivatives,XIV: New Procedure for the Preparation of 2,2-Dimethyl-2H-chromenes

2,2-Dimethyl-4-methoxychromans (1–12) have been converted into 2,2-dimethyl-2H-chromenes (13–24) in acidic media.     

Radical Reactivity of the Biradical [⋅P(μ-NTer)2P⋅] and Isolation of a Persistent Phosphorus-Cantered Monoradical [⋅P(μ-NTer)2P-Et]

The activation of C−Br bonds in various bromoalkanes by the biradical [⋅P(μ-NTer)₂P⋅] ( 1 ) (Ter=2,6-bis-(2,4,6-trimethylphenyl)-phenyl) is reported, yielding trans-addition products of the type [Br−P(μ-NTer)₂P−R] ( 2 ), so-called 1,3-substituted cyclo-1,3-diphospha-2,4-diazanes. This addition reaction, which represents a new easy approach to asymmetrically substituted cyclo-1,3-diphospha-2,4-diazanes, was investigated mechanistically by different spectroscopic methods (NMR, EPR, IR, Raman); the results suggested a stepwise radical reaction mechanism, as evidenced by the in-situ detection of the phosphorus-centered monoradical [⋅P(μ-NTer)₂P-R].< To provide further evidence for the radical mechanism, [⋅P(μ-NTer)₂P-Et] ( 3Et ⋅) was synthesized directly by reduction of the bromoethane addition product [Br-P(μ-NTer)₂P-Et] ( 2 a ) with magnesium, resulting in the formation of the persistent phosphorus-centered monoradical [⋅P(μ-NTer)₂P-Et], which could be isolated and fully characterized, including single-crystal X-ray diffraction. Comparison of the EPR spectrum of the radical intermediate in the addition reaction with that of the synthesized new [⋅P(μ-NTer)₂P-Et] radical clearly proves the existence of radicals over the course of the reaction of biradical [⋅P(μ-NTer)₂P⋅] ( 1 ) with bromoethane. Extensive DFT and coupled cluster calculations corroborate the experimental data for a radical mechanism in the reaction of biradical [⋅P(μ-NTer)₂P⋅] with EtBr. In the field of hetero-cyclobutane-1,3-diyls, the demonstration of a stepwise radical reaction represents a new aspect and closes the gap between P-centered biradicals and P-centered monoradicals in terms of radical reactivity.     

Fermion family recurrences in the Dyson–Schwinger formalism

We study the multiple solutions of the truncated propagator Dyson–Schwinger equation for a simple fermion theory with Yukawa coupling to a scalar field. Upon increasing the coupling constant g, other parameters being fixed, more than one non-perturbative solution breaking chiral symmetry becomes possible and we find these numerically. These “recurrences” appear as a mechanism to generate different fermion generations as quanta of the same fundamental field in an interacting field theory, without assuming any composite structure. The number of recurrences or flavors is reduced to the question of the value of the Yukawa coupling, and it has no special profound significance in the standard model. The resulting mass function can have one or more nodes and the measurement that potentially detects them can be thought of as a collider-based test of the virtual dispersion relation for the charged lepton member of each family. This requires the three independent measurements of the charged lepton’s energy, three-momentum and off-shellness. We illustrate how this can be achieved for the (more difficult) case of the tau lepton. PACS 12.15.Ff; 11.30.Rd