Generation of hyperentangled photon pairs

We experimentally demonstrate the first quantum system entangled in every degree of freedom (hyperentangled). Using pairs of photons produced in spontaneous parametric down-conversion, we verify entanglement by observing a Bell-type inequality violation in each degree of freedom: polarization, spatial mode, and time energy. We also produce and characterize maximally hyperentangled states and novel states simultaneously exhibiting both quantum and classical correlations. Finally, we report the tomography of a 2 x 2 x 3 x 3 system (36-dimensional Hilbert space), which we believe is the first reported photonic entangled system of this size to be so characterized.     

Maximally entangled mixed states: creation and concentration

Using correlated photons from parametric down-conversion, we extend the boundaries of experimentally accessible two-qubit Hilbert space. Specifically, we have created and characterized maximally entangled mixed states that lie above the Werner boundary in the linear entropy-tangle plane. In addition, we demonstrate that such states can be efficiently concentrated, simultaneously increasing both the purity and the degree of entanglement. We investigate a previously unsuspected sensitivity imbalance in common state measures, i.e., the tangle, linear entropy, and fidelity.     

An open source protein gel documentation system for proteome analyses

Data organization and data mining represents one of the main challenges for modern high throughput technologies in pharmaceutical chemistry and medical chemistry. The presented open source documentation and analysis system provides an integrated solution (tutorial, setup protocol, sources, executables) aimed at substituting the traditionally used lab-book. The data management solution provided incorporates detailed information about the processing of the gels and the experimental conditions used and includes basic data analysis facilities which can be easily extended. The sample database and User-Interface are available free of charge under the GNU license from http://webber.physik.uni-freiburg.de/~fallerd/tutorial.htm.     

Hydrogenolysis of [PhBP3]Fe[triple bond]N-p-tolyl: probing the reactivity of an iron imide with H2

This paper describes the reductive hydrogenolysis of a low-spin (S = 1/2) iron(III) imide. Pseudotetrahedral [PhBP3]FeIIIN-p-tolyl is reduced by hydrogen at ambient temperature and pressure in benzene solution. The reduction appears to proceed in a stepwise fashion. An intermediate S = 2 iron(II) anilide, [PhBP3]Fe(N(H)-p-tolyl), is observed and has been independently generated and structurally characterized. Prolonged hydrogenolysis in benzene results in the complete hydrogenolysis of the Fe-N linkage to release H2N-p-tolyl. The major iron-containing product formed from this step is the diamagnetic cyclohexadienyl complex, [PhBP3]Fe(eta5-cyclohexadienyl), which has also been independently prepared and structurally characterized. Evidence is presented to suggest that the final [PhBP3]Fe(eta5-cyclohexadienyl) product is formed via benzene insertion into a reactive [PhBP3]FeII-H intermediate.     

A Characterization of Subspaces of Weakly Compactly Generated Banach Spaces

It is proved that a Banach space X is a subspace of a weaklycompactly generated Banach space if and only if, for every >0,X can be covered by a countable collection of bounded closedconvex symmetric sets where the weak^* closure in X^** of eachof them lies within the distance from X. A new short functional-analyticproof of the known result that a continuous image of an Eberleincompact is Eberlein is given as a corollary.     

MSTAR: a submicrometer absolute metrology system

The Modulation Sideband Technology for Absolute Ranging (MSTAR) sensor permits absolute distance measurement with subnanometer accuracy, an improvement of 4 orders of magnitude over current techniques. The system uses fast phase modulators to resolve the integer cycle ambiguity of standard interferometers. The concept is described and demonstrated over target distances up to 1 m. The design can be extended to kilometer-scale separations.     

Pump modulation frequency resolved excited state absorption spectra in Tm<Superscript>3+</Superscript> doped YLF

Excited state absorption (ESA) in a 1% doped Tm:YLF crystal in the range from 1000 nm to 1300 nm is reported. In this spectral range, three ESA bands are expected: ³F₄³F₂ (from 1040 nm to 1096 nm), ³F₄³F₃ (from 1111 nm to 1169 nm), and ³H₄¹G₄ (from 1118 nm to 1240 nm). In a conventional continuous wave ESA setup only the first two bands are observed because the lifetime of the ³F₄ level is much longer (15.6 ms) than the lifetime of the ³H₄ level (1.56 ms). In order to observe the ³H₄¹G₄ ESA band, pump modulation dependent measurements were performed, where the modulation frequency of the pump selects the ESA signal to be measured. PACS 42.62.Fi; 42.70.Hj; 78.20.Ci; 78.20.Bh     

Absence of 2kF splitting in the diffuse scattering from Cu3Au at the (001) surface

We report a new type of short-range order correlations at the (001) surface of Cu3Au which no longer produces the 2k(F)-splitting characteristic for the bulk short-range order scattering. We present the temperature dependence of this phenomenon and a theoretical interpretation of its origin. We argue that this new surface effect is caused by a drastic change of the strain-induced interactions at the surface.     

Dinitrogen chemistry from trigonally coordinated iron and cobalt platforms

This report establishes that trigonally coordinated "[PhBPiPr3]M" platforms (M = Fe, Co) will support both pi-acidic (N2) and pi-basic (NR) ligands at a fourth binding site. The N2 complexes of iron that are described are the first thoroughly characterized examples to exhibit a 4-coordinate geometry. Methylation of monomeric {Fe0(N2)-} and {Co0(N2)-} species successfully derivatizes the beta-N atom of the coordinated N2 ligand and affords the diazenido products {FeII(N2Me)} and {CoII(N2Me)}, respectively. One-electron oxidation of the mononuclear M0(N2)- species produces dinuclear and synthetically versatile MI(N2)MI complexes. These latter species provide clean access to the chemistry of the "[PhBPiPr3]MI" subunit. For example, addition of RN3 to MI(N2)MI results in oxidative nitrene transfer to generate [PhBPiPr3]MNR with concomitant N2 release.