Chern–Simons–Rozansky–Witten topological field theory

We construct and study a new topological field theory in three dimensions. It is a hybrid between Chern–Simons and Rozansky–Witten theory and can be regarded as a topologically-twisted version of the N=4$N=4$d=3$d=3$ supersymmetric gauge theory recently discovered by Gaiotto and Witten. The model depends on a gauge group G and a hyper-Kähler manifold X with a tri-holomorphic action of G. In the case when X is an affine space, we show that the model is equivalent to Chern–Simons theory whose gauge group is a supergroup. This explains the role of Lie superalgebras in the construction of Gaiotto and Witten. For general X, our model appears to be new. We describe some of its properties, focusing on the case when G is simple and X is the cotangent bundle of the flag variety of G. In particular, we show that Wilson loops are labeled by objects of a certain category which is a quantum deformation of the equivariant derived category of coherent sheaves on X.     

Three-dimensional particle imaging by defocusing method with an annular aperture

We propose an annular-aperture-based defocusing technique for three-dimensional (3D) particle metrology from a single camera view. This simple configuration has high optical efficiency and the ability to deal with overlapped defocused images. Initial results show that an uncertainty in depth of 23 microm can be achieved over a range of 10 mm for macroscopic systems. This method can also be applied in microscopy for the measurement of fluorescently doped microparticles, thus providing a promising solution for 3D flow metrology at both macroscales and microscales.     

A convenient synthesis of substituted 3-bromotetrahydrofurans from homoallylic alcohols

Substituted 3-bromotetrahydrofurans were prepared from homoallylic alcohols via bromination and cyclization in methanol in the presence of potassium carbonate.     

Sopra le estremali relative ad integrali curvilinei dello spazio in forma parametrica

Sunto Nel presente lavoro l' A. stabilisce le equazioni di Eulero relative agli integrali curvilinei e rileva alcune proprietà delle estremali relative alla funzione F, occupandosi in particolare dell'esistenza delle derivate successive delle funzioni da cui le estremali sono definite.     

Shock-induced arrhythmogenesis in the myocardium

The focus of this article is the investigation of the electrical behavior of the normal myocardium following the delivery of high-strength defibrillation shocks. To achieve its goal, the study employs a complex three-dimensional defibrillation model of a slice of the canine heart characterized with realistic geometry and fiber architecture. Defibrillation shocks of various strengths and electrode configurations are delivered to the model preparation in which a sustained ventricular tachycardia is induced. Instead of analyzing the post-shock electrical events as progressions of transmembrane potential maps, the study examines the evolution of the postshock phase singularities (PSs) which represent the organizing centers of reentry. The simulation results demonstrate that the shock induces numerous PSs the majority of which vanish before the reentrant wavefronts associated with them complete half of a single rotation. Failed shocks are characterized with one or more PSs that survive the initial period of PS annihilation to establish a new postshock arrhythmia. The increase in shock strength results in an overall decrease of the number of PSs that survive over 200 ms after the end of the shock; however, the exact behavior of the PSs is strongly dependent on the shock electrode configuration. (c) 2002 American Institute of Physics.     

Water-assisted alkaline hydrolysis of monobactams: a theoretical study

A theoretical study of the water-assisted alkaline hydrolysis of 2-azetidinone, 3-formylamino-2-azetidinone and 3-formylamino-2-azetidine-1-sulfonate ion is carried out at the B3LYP/6-31+G* level. The effect of bulk solvent is taken into account using the PCM solvation model while specific solvent effects are represented by the inclusion of an ancillary water molecule along the reaction profile. The calculated free energy barriers in solution are in reasonable agreement with experimental values. The observed substituent effects due to the presence of the 3-formylamino and the SO(3) groups attached to the beta-lactam ring are crucial factors determining the hydrolysis of monobactam antibiotics.     

Noncovalent imprinting in the shell of core-shell nanoparticles

Propranolol was imprinted using noncovalent interactions in the shell of core-shell nanoparticles prepared by aqueous emulsion polymerization in the presence and absence of toluene. The imprinted particles were characterized, and their capacity to rebind propranolol from both organic and aqueous media was analyzed. Results showed that the amount of template incorporated into the polymer and the presence of toluene as a "porogenic" agent influenced the ability of the nanoparticles obtained to rebind propranolol. The presence of toluene during imprinting increased rebinding by about 2-fold in buffer and by 3-fold in toluene, compared with similar materials made in the absence of toluene during imprinting. It also influenced the final surface area of the particles. Binding site affinity, assessed by radioligand displacement, was measured as IC50 values of about 1-10 microM. This compares with about 3 microM for bulk polymer made with a similar composition. Finally, to demonstrate the advantages of structured particles for analytical applications a new property, fluorescence, was incorporated into the core of the particles without interfering with the imprinted shell and its ability to rebind propranolol.     

Near Infrared Luminescence of Lanthanides in Complexes with Organic Dyes

Spectral-luminescence characteristics of Yb³⁺ and Nd³⁺ ions in water solutions of their complexes with some organic dyes of sulfophenylphthalexones group have been considered. Complexes can be efficiently excited with visible light (_exc = 532 nm). 4f-Luminescence as a result of energy transfer from the dye moiety to the lanthanide ion was shown. Complexation of new polydentate ligand L of sulfophenylphthalexones type increases the luminescence lifetimes because of the reduced solvation of the ion by water. They were determined as 12.60 s for complex Yb-L and 1.45 s for Nd-L.