Holographic chemical vapor sensor

A holographic interferometer senses vapor-induced optical path length changes in polymer or other chemically sensitive films. The interferometer is inherently sensitive to changes in chemical vapor content, self-compensates for drifts, and accommodates a large array of sensor elements. A sniff-locked-loop synchronous detection method takes advantage of the interferometer's rapid response to achieve vapor concentration sensitivity in the parts-per-billion (ppb, parts in 10(9)) range. We demonstrate, for example, 40 ppb sensitivity to ethyl alcohol using poly(N-vinyl pyrrolidone) with a measurement time of 5 s.     

Ma?analytische Methoden

Ohne Zusammenfassung     

Aberration-correction results from a segmented microelectromechanical deformable mirror and a refractive lenslet array

Quadratic aberration is successfully corrected with a segmented microelectromechanical deformable mirror in conjunction with a refractive lenslet array. Use of the lenslet array greatly improves the effective fill factor of the correcting element. Experimental results show correction approaching the diffraction limit for an extreme spherical aberration.     

Comparison of inter- and intramolecular cyclodextrin complexes

Abstract

We present the first comparative steady-state and time-resolved fluorescence studies of inter- and intramolecular cyclodextrin complexes. Specifically, we report equilibrium and kinetic results for dansyl-glycine complexed with β-cyclodextrin (intermolecular) and the dansyl-glycine-β-cyclodextrin adduct (intramolecular). The fluorescence intensity decay profile for the intermolecular system is best described by a discrete triple exponential decay law. This is consistent with stepwise 1:1 and 2:1 (β-cyclodextrin:guest) inclusion complexation. Equilibrium constants are in line with previous results on similar species. In contrast, we found that the intramolecular case was described by a doubly exponential decay law—consistent with a single intramolecular inclusion complex. Displacement experiments, with borneol, confirm the simplicity of the intramolecular complex. In all cases, continuous distribution models failed to fit the experimental data.     

5-Bromobarbituric Acid : A Mild and Selective Monobrominating Agent Employed in the Synthesis of the Gastrin Antagonist GR174152

5-Bromobarbituric acid (5) is a convenient reagent for the selective bromination of cyclic imine 3. A facile, in situ synthesis of this reagent involving a disproportionation reaction between barbituric acid and dibromobarbituric acid is described.