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1.
P. Paasche T. Valenzuela D. Biswas C. Angelescu G. Werth 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2002,18(3):295-300
We have examined experimentally the motional spectrum of an electron cloud confined in a Penning trap. When the axial oscillation
is excited by a radio frequency field the resonance exhibits a double structure. Both components depend differently on the
number of trapped electrons and have different shape and width. We conclude that one of them corresponds to the excitation
of the individual electrons while the other is the center-of-mass mode of the cloud. The threshold behaviour of the center-of-mass
resonance suggests that it is a parametric instability of a Mathieu type equation of motion.
Received 11 July 2001 and Received in final form 12 November 2001 相似文献
2.
3.
4.
Le Faou JH Suomijärvi T Blumenfeld Y Piattelli P Agodi C Alamanos N Alba R Auger F Bellia G Chomaz P Coniglione R Del Zoppo A Finocchiaro P Frascaria N Gaardhoje JJ Garron JP Gillibert A Lamehi-Rachti M Liguori-Neto R Maiolino C Migneco E Russo G Roynette JC Santonocito D Sapienza P Scarpaci JA Smerzi A 《Physical review letters》1994,72(21):3321-3324
5.
Richard Ley D. Hagena D. Weil G. Werth W. Arnold H. Schneider 《Hyperfine Interactions》1994,89(1):327-341
Electric dipole transitions in the microwave range have been induced between the fine-structure levels of positronium in the excited staten=2. As an indication of the transitions, we used the increase in Lyman- radiation when the metastable 23S1-level is depopulated. The results for the transitions 23S123P0,1,2 are
0=18499.65±1.20±4.00 MHz,
1=13012.42 ±0.65±1.54 MHz and
2=8624.38±0.54±1.40 MHz. The first error is statistical and the second systematic. The precision of the present measurement has improved by a factor of 3, compared to previous data. Recent bound state QED-calculations have been extended to the orderR
t8
4ln
–1. The not yet completely calculated orderR
t8
4 is estimated to contribute less than 1 MHz. Our experimental results are in good agreement with theory. By applying a weak magnetic field, we were able to observe the transition 23S121P1 which is strictly forbidden byC-invariance in zero field. Our result, corrected for Zeeman- and motional Starkeffect, is
3=11180.0±5.0±4.0 MHz. An upper limit for theC-violating matrix element of
MHz could be deduced. Our experiment used moderated slow positrons from the bremsstrahlung and pair production of a pulsed electron linear accelerator (TEPOS facility at the university of Giessen). 相似文献
6.
Akiba Y Beavis D Beery P Britt HC Budick B Chasman C Chen Z Chi CY Chu YY Cianciolo V Cole BA Costales JB Crawford HJ Cumming JB Debbe R Engelage J Fung SY Gonin M Gushue S Hamagaki H Hansen O Hayano RS Hayashi S Homma S Kaneko H Kang J Kaufman S Kehoe WL Kurita K Ledoux RJ Levine MJ Miake Y Morrison DP Morse RJ Moskowitz B Nagamiya S Namboodiri MN Nayak TK Olness J Parsons CG Remsberg LP Roehrich D Rothschild P Sakurai H Sangster TC Seto R Soltz R Stankus P Steadman SG Stephans GS Sung T 《Physical review letters》1996,76(12):2021-2024
7.
Garcia Ruano JL Alemparte C Martin Castro AM Adams H Rodriguez Ramos JH 《The Journal of organic chemistry》2000,65(23):7938-7943
The behavior of (Z)-3-p-tolylsulfinylacrylonitrile (1) as a chiral dienophile has been evaluated from its reactions with furan and acyclic dienes. Electrostatic interactions of the cyano group with the sulfinyl one restrict the conformational mobility around the C-S bond, thus controlling the pi-facial selectivity, which is almost complete in all cases, the approach of the diene from the less-hindered face of the dienophile (that bearing the lone electron pair) in the predominant rotamer being the favored one. The regioselectivity is also completely controlled by the cyano group. Additionally, the reactivity of compound 1 as well as its endo-selectivity are both higher than those observed for the corresponding (Z)-3-sulfinylacrylates, thus proving the potential of sulfinylnitriles as chiral dienophiles. 相似文献
8.
Guo Zhong Li R. Poggiani G. Testera G. Werth 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1991,22(1):375-382
An ion cloud in a Penning trap can be cooled by adiabatic expansion by reducing the trap's magnetic and electric fields. We treat the ion cloud as a classical gas and obtain the relations between the temperature and the trapping fields. This cooling method may be useful in trapping and cooling of antiprotons with the aim of measuring the gravitational accleration of anti-protons and other experiments on heavy ions. 相似文献
9.
Lenhart JL van Zanten JH Dunkers JP Zimba CG James CA Pollack SK Parnas RS 《Journal of colloid and interface science》2000,221(1):75-86
Silane coupling agents are commonly applied to glass fibers to promote fiber/resin adhesion and enhance durability in composite parts. In this study, a coupling agent multilayer on glass was doped with trace levels of the dimethylaminonitrostilbene (DMANS) fluorophore. The fluorophore was immobilized on the glass surface by tethering the molecule to a triethoxy silane coupling agent, creating the DMANS/silane coupling agent molecule (DMSCA). DMSCA was then diluted with commonly used coupling agents and grafted to a glass microscope coverslip to create a model composite interface. A 53-nm blue shift in fluorescence from the immobilized DMSCA can be followed during cure of an epoxy resin overlayer, giving this technique potential to monitor the properties of the fiber/resin interface during composite processing. Contact angle measurements on these coupling agent layers were similar in the presence or absence of the DMSCA molecule, suggesting that trace levels of the fluorescent probe did not affect the structure of the layer. The immobilized DMSCA molecule behaved similarly to the DMANS precursor in solution. Both showed longer wavelength fluorescence in more polar environments. Copyright 2000 Academic Press. 相似文献
10.
Dr. Yong Guo Dr. Wengang Li Dr. Jingjing Yan Dr. Basem Moosa Dr. Ma'an Amad Prof. Charles J. Werth Prof. Niveen M. Khashab 《化学:亚洲杂志》2012,7(12):2842-2847
Metal‐free fullerene (C60) was found to be an effective catalyst for the reduction of azo groups in basic aqueous solution under UV irradiation in the presence of NaBH4. Use of NaBH4 by itself is not sufficient to reduce the azo dyes without the assistance of a metal catalyst such as Pd and Ag. Experimental and theoretical results suggest that C60 catalyzes this reaction by using its vacant orbital to accept the electron in the bonding orbital of azo dyes, which leads to the activation of the N?N bond. UV irradiation increases the ability of C60 to interact with electron‐donor moieties in azo dyes. 相似文献