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11.
S. Descotes N.H. Fuchs L. Girlanda J. Stern 《The European Physical Journal C - Particles and Fields》2002,24(3):469-483
The recently published E865 data on charged decays and phases are reanalyzed to extract values of the two S-wave scattering lengths, of the subthreshold parameters and , of the low-energy constants and as well as of the main two-flavour order parameters: and in the limit taken at the physical value of the strange quark mass. Our analysis is exclusively based on direct experimental information
on phases below 800 MeV and on the new solutions of the Roy equations by Ananthanarayan et al. The result is compared with the
theoretical prediction relating 2a
0
0-5a
0
2 and the scalar radius of the pion, which was obtained in two-loop Chiral Perturbation Theory. A discrepancy at the 1- level is found and commented upon.
Received: 11 December 2001 / Revised version: 28 March 2002 / Published online: 7 June 2002 相似文献
12.
R. Rehm M. Walther J. Schmitz J. Fleißner F. Fuchs J. Ziegler W. Cabanski 《Opto-Electronics Review》2006,14(1):19-24
The first fully operational mid-IR (3–5 μm) 256×256 IR-FPA camera system based on a type-II InAs/GaSb short-period superlattice
showing an excellent noise equivalent temperature difference below 10 mK and a very uniform performance has been realized.
We report on the development and fabrication of the detecor chip, i.e., epitaxy, processing technology and electro-optical
characterization of fully integrated InAs/GaSb superlattice focal plane arrays. While the superlattice design employed for
the first demonstrator camera yielded a quantum efficiency around 30%, a superlattice structure grown with a thicker active
layer and an optimized V/III BEP ratio during growth of the InAs layers exhibits a significant increase in quantum efficiency.
Quantitative responsivity measurements reveal a quantum efficiency of about 60% for InAs/GaSb superlattice focal plane arrays
after implementing this design improvement.
The paper presented there appears in Infrared Photoelectronics, edited by Antoni Rogalski, Eustace L. Dereniak, Fiodor F. Sizov, Proc. SPIE Vol. 5957, 595707 (2005). 相似文献
13.
Colloid and Polymer Science - Nach einer Aufzählung der verschiedenen Arten von zwischenmolekularen Kräften und dem Hinweis auf die Gültigkeitsgrenze der bestehenden Vorstellungen... 相似文献
14.
Martin Fuchs 《manuscripta mathematica》1987,58(3):377-380
Considering discrete groups G only, we present an elementary proof of the familiar equivalence of the category of G-spaces (with maps equivariant up to homotopy) and the category of Borel fibrations over BG. 相似文献
15.
J. Fuchs 《Zeitschrift fur Physik C Particles and Fields》1987,35(1):89-95
We consider conformally and Kac-Moody invariant theories based on the groupsG=G(N)×G(Ñ) whereG(N) is any of the classical groups. For the valuesk=Ñ, \(\tilde k = N\) of the Kac-Moody central charges, the monodromy problem involved in the computation of the four point function for primary fields in the defining representation ofG possesses two distinct solutions. As a consequence, the WZW theory onG (with an additionalU(1) factor ifG(N)=SU (N)) cannot be equivalent to a theory of free fermions. 相似文献
16.
A computational study ab initio of the conformational dependence of proton affinities of 2-methoxyethoxide (MEO), dimethoxyethane (DME), and 1,4-dioxane has been carried out at the MP2/6-31+G level of theory. The results were discussed in comparison with reference systems, from simple alkoxides and ethers to anomeric moieties, in open, cyclic, and bicyclic molecules. The COCCOC species are stronger bases than the COCOC (anomeric) ones and approach regular ethers in their strength. The gauche forms in MEO and DME are altogether stronger bases than the anti forms, and anti (equatorial) protonation is preferred over gauche (axial), unless ditopic protonation is possible, like in aga-DME or cis-tetraoxadecalin. The gauche effect plays a significant role in the formation, relative stability, and reactivity of the charged species. 相似文献
17.
[reaction: see text]. A variety of heterocyclic ring systems can be prepared by subjecting N-aryl-substituted 5-amido-1,3-dioxins to Lewis acids. The reactions proceed via catalyzed retrocycloadditions to afford 2-amidoacroleins and concomitant regioselective electrophilic aromatic substitution reactions. The transformation is also successful using dioxins with amides that are within the incipient ring to afford the analogous lactams. 相似文献
18.
E R Werner G Werner-Felmayer D Fuchs A Hausen G Reibnegger G Wels J J Yim W Pfleiderer H Wachter 《Journal of chromatography. A》1991,570(1):43-50
An assay for 6-pyruvoyl tetrahydropterin synthase, the second enzyme in the conversion of guanosine triphosphate into tetrahydrobiopterin, has been developed. Cell extracts were incubated with enzymatically prepared dihydroneopterin triphosphate (80 microM) in the presence of Mg2+ (12 mM), excess sepiapterin reductase (EC 1.1.1.153) (2 nmol/min) and NADPH (2 mM). 6-Pyruvoyl tetrahydropterin, the product of the reaction, was thus converted into tetrahydrobiopterin. After oxidation of the reduced biopterin derivatives in acidic iodine solution, biopterin was enriched and separated from the abundant neopterin phosphates by solid-phase extraction on a strong cation exchanger. Biopterin was then directly eluted on a reversed-phase liquid chromatographic column and detected fluorimetrically using excitation at 353 nm and emission at 438 nm. The biopterin concentrations formed by the coupled enzyme reaction increased linearly with incubation times up to 90 min. The assay allows the quantification of 6-pyruvoyl tetrahydropterin synthase in cultured human cells. 相似文献
19.
The first total synthesis of racemic perophoramidine is described. The key step features the highly stereoselective introduction of the vicinial quaternary centers via base-promoted carbon-carbon bond formation between a 3-alkylindole and a 3-bromo-3-alkylindolin-2-one. This transformation presumably proceeds through a conjugate addition or Diels-Alder cycloaddition of the 3-alkylindole with a 3-alkylindol-2-one intermediate. 相似文献
20.
H. Weiner H.-J. Lunk J. Fuchs B. Ziemer R. Stsser C. Pietzsch P. Reich 《无机化学与普通化学杂志》1991,594(1):191-201
Synthesis and Structure Studies of Ba2H[α-FeO4W12O36] · 26 H2O The heteropolyanion compound Ba2H[α-FeO4W12O36] · 26 H2O (I) crystallizes in the tetragonal space group P4 n2 with the lattice parameters a = 12.398(6), c = 18.721(6) Å; Z = 2; Dx = 4.128 g · cm?3. The structure was solved on a twinned crystal from 1029 observed reflections and refined to an index R of 7.6%. The calculations were done by means of a modified ORFLS-programme by Eitel and Bärnighausen. The heteropolyanion [α-FeO4W12O36]5? has the well known α-Keggin structure. The average distance of the four central oxygen atoms to the FeIII position (0, 0, 0) is 1.84 Å. The angles ? O? Fe? O are 112.3° (4X) and 103.9 (2X), respectively, which leads to an disphenoidal distortion of the FeO4 tetrahedron. The powder and single crystal ESR spectra of I show the anisotropy of the FeIII fine structure transition 1/2 ? ?1/2. The Mößbauer spectra confirm the tetragonal distortion of the central FeO4 tetrahedron (quadrupole splitting Δ ≈ 0.50 mm · s?1). 相似文献