An apporach for the sensing of small amounts of chemical and biochemical material is presented.A frequency selective surface (FSS) made from asymmetric split ring resonators (aDSR) is excited with free space radiation. Due to interference effects a resonance occurs with a steep flank in the frequency response which is shifted upon dielectric loading. Utilizing a strong E-field concentration by selective loading the detection of very small amounts of probe material becomes possible. The functionality is proven by numerical simulation and the optimization of structure and loading is performed.

The orientation of the S 1 r S 0 π,π* transition dipole moments of oxonine (Ox + ), pyronine (Py + ), and POPOP (5,5′-diphenyl-2,2′-p-phenylenebis(oxazole)) in the channels of zeolite L crystals was investigated by means of fluorescence microscopy and single-crystal imaging. Qualitative observations led to the result that the transition moment of POPOP is aligned along the c-axis of the hexagonal crystals whereas the fluorescence of Ox + and Py + is not. More detailed investigations on Ox + showed a cone-shaped distribution of the transition moments with a half-cone angle of 72°. The orientation of the transition dipole moment for all of these molecules is parallel to the molecules' long axis. We found by means of space-filling arguments that POPOP, the van der Waals length of which is about 21 Å, can only be aligned along the channel axis. This is in full agreement with the observed fluorescence anisotropy. For Ox + and Py + , geometrical arguments based on the zeolite L structure give room for only two possible arrangements of the molecules' long axis: a half cone angle of up to 40°for Ox + and up to 30°for Py + , and an angle of about 90°for both of them with respect to the c-axis of zeolite L. The surprising discrepancy between geometrical considerations and the results of the fluorescence measurements can be explained by assuming that Ox + and Py + are exposed to a considerable anisotropic electrical field in the zeolite channels.

A novel high-resolution stage scanning confocal microscope for fluorescence microscopy and spatially resolved spectroscopy with a high numerical aperture (NA 1) parabolic mirror objective is investigated. A spatial resolution close to the diffraction limit is achieved. As microscopic fluorescent test objects, dye-loaded zeolite microcrystals (diameter approx. 0.4 microm) and single fluorescent molecules were used. Confocal fluorescence images show a spatial resolution of .x = 0.8 . both at room temperature and at 1.8 K. Imaging of a quasi-point light source and focusing by the parabolic mirror were investigated experimentally and theoretically. Deviations between the theoretical results for a perfect parabolic mirror and the experimental results can be attributed to small deviations of the mirror profile from an ideal parabola.