Fluorescence tomography with simulated data based on the equation of radiative transfer

The quantification of a nonuniform quantum yield or fluorophore absorption distribution is of major interest in molecular imaging of biological tissue. We introduce what is believed to be the first fluorescence image reconstruction algorithm based on the equation of radiative transfer that recovers the spatial distribution of light-emitting fluorophores inside a highly scattering medium from measurements made on the surface of the medium. We obtain images of either the quantum yield or the fluorophore absorption.     

Fabrication of ridge waveguides in zinc-substituted lithium niobate by means of ion-beam enhanced etching

We present results on the fabrication and characterization of ridge waveguides in zinc-substituted lithium niobate. High-quality waveguides were fabricated by a combination of liquid-phase epitaxy and multiple applications of ion-beam enhanced etching. The two major demands on ridge waveguides, a very low side-wall roughness and a rectangle shape with side-wall angles close to 90 degrees , were realized simultaneously by using this technique. Single-mode waveguiding at a wavelength of 1064 nm was demonstrated with attenuation values of 0.9 dB/cm.     

Über die Tribromomangan(II)-Säure und deren Komplex mit Pyridin

Tribromomanganese(II) acid has been prepared for the first time and will be described. A complex of the acid with pyridine was obtained and its UV, visible, IR and¹H-NMR spectra will be reported.     

Electronic States of 1,5-Cyclooctadiyne Radical Cation and of Related Systems: The electronic structure of cis-bent carbon-carbon triple bonds

The photoelectron spectra of 1,5-cyclooctadiyne ( 2 ) and of 1,6-dithiacyclodeca-3,8-diyne ( 3 ) have been recorded. The first four ( 2 ) or six ( 3 ) PE. bands have been assigned as follows; in increasing order of ionization potentials: The relative sequence and the positions of the PE. bands are explained in terms of through-bond and through-space interactions between the basis π-orbitals and σ-orbitals of appropriate symmetry behaviour. An analysis of the PE. spectroscopic data for cyclooctyne ( 1 ) and for ( 2 ) indicates that a cis-bend of the acetylene moiety by θ < 20° leads to a split in energy of the in-plane and out-of-plane basis π-orbitals which is smaller than ∽ 0.2 eV. This is in agreement with the predictions derived from semiempirical models (MINDO/2, SPINDO) and qualitative orbital arguments. However, it is shown by using orbital localization procedures, that the rationales underlying the two semiempirical models differ significantly.