Performance of the far‐IR beamline of the 6 MeV tabletop synchrotron light source

The performance of the far‐infrared (FIR) beamline of the 6 MeV tabletop synchrotron light source MIRRORCLE‐6FIR dedicated to far‐infrared spectroscopy is presented. MIRRORCLE‐6FIR is equipped with a perfectly circular optical system (PhSR) placed around the 1 m‐long circumference electron orbit. To illustrate the facility of this light source, the FIR output as well as its spectra were measured. The optimum optical system was designed by using the ray‐tracing simulation code ZEMAX. The measured FIR intensity with the PhSR in place is about five times higher than that without the PhSR, which is in good agreement with the simulation results. The MIRRORCLE‐6FIR spectral flux is compared with a standard thermal source and is found to be 1000 times greater than that from a typical thermal source at ～15 cm^?1. It is also observed that the MIRRORCLE‐6FIR radiation has a highly coherent nature. The broadband infrared allows the facility to reach the spectral range from 10 cm^?1 to 100 cm^?1. MIRRORCLE‐6FIR, owing to a large beam current, the PhSR mirror system, a large dynamic aperture and small ring energy, can deliver a bright flux of photons in the FIR/THz region useful for broadband spectroscopy.     

Analytic calculation of the lineshapes in polarization spectroscopy of rubidium

This paper reports on analytic calculations of the lineshapes for polarization spectroscopy of rubidium atoms. Under the use of a weak circularly polarized pump beam, the time-dependent population of each magnetic sublevel was obtained analytically from the rate equations up to the lowest order of the pump beam intensity, and the associated circular birefringence experienced by a counterpropagating probe beam was calculated. In particular, analytic forms of the polarization spectroscopy spectra were obtained for ⁸⁷Rb and ⁸⁵Rb atoms using the mean transit time crossing the pump beam, and the analytic results were compared with the numerical data, experimental results and Nakayama model’s results, showing a good agreement one another.     

Reflection characteristics of a copper metal-organic chemical-vapor-deposited thin film for vertical micromirror applications

We introduce Cu metal-organic chemical-vapor deposition as a potential means of conformal metal coating of the sidewalls of micromachined vertical mirrors. The optimal process temperature was experimentally found to be 215 degrees C, which gives high step coverage of better than 90%, and the surface roughness was less than 27 nm. The roughness, measured with an atomic force microscope, will induce a scattering loss less than 0.12 dB, which is small enough for vertical micromirror application. The experimental reflectances of Cu thin film were measured with a distributed-feedback laser (1550 nm) and found to be greater than 0.9 for incidence angles of 22.5 degrees and 45 degrees , and these reflectances were in good agreement with theoretical values.     

Time-delayed spatial patterns in a two-dimensional array of coupled oscillators

We investigated the effect of time delays on phase configurations in a set of two-dimensional coupled phase oscillators. Each oscillator is allowed to interact with its neighbors located within a finite radius, which serves as a control parameter in this study. It is found that distance-dependent time delays induce various patterns including traveling rolls, squarelike and rhombuslike patterns, spirals, and targets. We analyzed the stability boundaries of the emerging patterns and briefly pointed out the possible empirical implications of such time-delayed patterns.     

Enantioselective synthesis of bicyclo[3.1.0]hexane carbocyclic nucleosides via a lipase-catalyzed asymmetric acetylation. Characterization of an unusual acetal byproduct

The bicyclo[3.1.0]hexane scaffold can lock the conformation of a carbocyclic nucleoside into one of the two antipodal (north or south) conformations typical of conventional nucleosides that normally exist in a rapid, two-state equilibrium in solution. In a recent brief communication, we reported a practical method to access the requisite bicyclo[3.1.0]hexane pseudosugar for the north antipode via an intramolecular olefin-ketocarbene cycloaddition. The most attractive features of this synthesis was that a relatively complex synthon was obtained from simple and inexpensive starting materials and that the resulting racemic mixtures of purine nucleosides could be successfully resolved by adenosine deaminase (ADA) hydrolysis. In this work, we describe the development of a more general, lipase-catalyzed double-acetylation reaction, which could successfully resolve an earlier precursor, 4-(tert-butyldiphenylsilamethoxy)-1-(hydroxymethyl)bicyclo[3.1.0]hexan-2-ol [(+/-)-7], into enantiomerically pure (+)-diacetate 8 and (-)-monoacetate 9. The former diacetate was converted to the conformationally locked (north)-carbocyclic guanosine (+)-17 identical to the one obtained previously by ADA resolution. The present method represents a more general and efficient process applicable to the synthesis of all classes of (north) bicyclo[3.1.0]hexane nucleosides, including pyrimidine analogues. During the lipase-catalyzed resolution, we were able to demonstrate the presence of an unusual acetal-forming reaction that consumed small amounts of the unreactive monoacetate (-)-9. This side reaction was also enzyme-catalyzed and was triggered by the byproduct acetaldehyde generated during the reaction.     

Modes of binding interaction between viologen guests and the cucurbit[7]uril host

[structure: see text] Host-guest interactions between cucurbit[7]uril (CB7) and a series of dialkyl-4,4'-bipyridinium (viologen) dicationic guests were investigated by NMR spectroscopy. CB7 includes the aromatic nucleus of short chain viologens, but the mode of interaction is different with longer chain viologens due to the favorable hydrophobic interactions between the terminal alkyl substituents and the inner cavity of the host. A new pseudorotaxane was designed and synthesized on the basis of viologen-CB7 binding interactions.     

Electrogenerated chemiluminescence: Part XXVII. E.C.L. and electrochemical studies of selected laser dyes

The electrogenerated chemiluminescence (e.c.l.) and electrochemistry of the laser dyes, coumarin-2, coumarin-30, rhodamine-6G (perchlorate), rhodamine-B (perchlorate), oxazine-1 (perchlorate), and Nile Blue (perchlorate) were studied in acetonitrile using 0.1 M tetra-n-butylammonium perchlorate (TBAP) as a supporting electrolyte. Rather low intensity e.c.l. was obtained for all dyes except Nile Blue. A study of the electrochemical oxidation and reduction of coumarin-30, oxazine-1 and rhodamine-6G using cyclic voltammetry and controlled potential coulometry demonstrated that chemical side reactions of the electrogenerated reactants are responsible for the low e.c.l. efficiency. In several cases the one-electron transfer reaction at the electrode is followed by a dimerization reaction. The neutral free radical formed on reduction of oxazine-1 was investigated by electron spin resonance spectroscopy and coupling constants for it are reported. Some experiments in which the e.c.l. of mixtures of the dyes with rubrene or 9,10-diphenylanthracene were determined are also described.     

Kink-induced transport and segregation in oscillated granular layers

We use experiments and molecular dynamics simulations of vertically oscillated granular layers to study horizontal particle segregation induced by a kink (a boundary between domains oscillating out of phase). Counterrotating convection rolls carry the larger particles in a bidisperse layer along the granular surface to a kink, where they become trapped. The convection originates from avalanches that occur inside the layer, along the interface between solidified and fluidized grains. The position of a kink can be controlled by modulation of the container frequency, making possible systematic harvesting of the larger particles.