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1.
A. N. Bandura V. V. Chebotarev I. E. Garkusha V. A. Makhlay A. K. Marchenko D. G. Solyakov V. I. Tereshin S. A. Trubchaninov A. V. Tsarenko I. Landman 《Czechoslovak Journal of Physics》2004,54(3):C53
The paper presents experimental investigation of energy characteristics of the plasma streams generated with quasi—steady—state plasma accelerator QSPA Kh-50 and adjustment of plasma paramenters from the point of view its applicability for simulation of transient plasma heat loads expected for ITER disruptions and type I ELMs. Possibility of generation of high-power magnetized plasma streams with ion impact energy up to 0.6 keV, pulse length 0.25 ms and heat loads varied in wide range from 0.5 to 30 MJ/m2 has been demonstrated and some features of plasma interaction with tungsten targets in dependence on plasma heat loads are discussed. 相似文献
2.
One of the open questions in the geometry of line arrangements is to what extent does the incidence lattice of an arrangement determine its fundamental group. Line arrangements of up to 6 lines were recently classified by K.M. Fan (Michigan Math. J. 44(2) (1997) 283), and it turns out that the incidence lattice of such arrangements determines the projective fundamental group. We use actions on the set of wiring diagrams, introduced in (Garber et al. (J. Knot Theory Ramf.), to classify real arrangements of up to 8 lines. In particular, we show that the incidence lattice of such arrangements determines both the affine and the projective fundamental groups. 相似文献
3.
Uzi Vishne 《Archiv der Mathematik》2003,80(2):119-122
We prove that assuming enough roots of unity in the base field, a central simple algebra of exponent 2 which is split by a dihedral group, is also split by certain abelian groups. 相似文献
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Separation of lithium and potassium isotopes has been achieved using the isotopic differences in the radiofrequency spectrum. The isotope separation was studied in a supersonic molecular beam magnetic resonance spectrometer, and enrichment factors up to 30 obtained. 相似文献
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Intercalation of trioxatriangulenium ion in DNA: binding,electron transfer,x-ray crystallography,and electronic structure 总被引:1,自引:0,他引:1
Reynisson J Schuster GB Howerton SB Williams LD Barnett RN Cleveland CL Landman U Harrit N Chaires JB 《Journal of the American Chemical Society》2003,125(8):2072-2083
Trioxatriangulenium ion (TOTA(+)) is a flat, somewhat hydrophobic compound that has a low-energy unoccupied molecular orbital. It binds to duplex DNA by intercalation with a preference for G-C base pairs. Irradiation of intercalated TOTA(+) causes charge (radical cation) injection that results in strand cleavage (after piperidine treatment) primarily at GG steps. The X-ray crystal structure of TOTA(+) intercalated in the hexameric duplex d[CGATCG](2) described here reveals that intercalation of TOTA(+) results in an unusually large extension of the helical rise of the DNA and that the orientation of TOTA(+) is sensitive to hydrogen-bonding interactions with backbone atoms of the DNA. Electronic structure calculations reveal no meaningful charge transfer from DNA to TOTA(+) because the lowest unoccupied molecular orbital of TOTA(+), (LUMO)(T), falls in the gap between the highest occupied molecular orbital, (HOMO)(D), and the (LUMO)(D) of the DNA bases. These calculations reveal the importance of backbone, water, and counterion interactions, which shift the energy levels of the bases and the intercalated TOTA(+) orbitals significantly. The calculations also show that the inserted TOTA(+) strongly polarizes the intercalation cavity where a sheet of excess electron density surrounds the TOTA(+). 相似文献
9.
The reactions of a series of 5-alkyl-2-thiophenedithiocarboxylates with nickel(II) chloride afforded two types of complexes, blue nickel(II) complexes with two terminal dithiocarboxylate ligands, [Ni(S2CTR)2] and violet nickel(II) complexes with perthio- and dithiocarboxylate ligands, [Ni(S2CTR)(S3CTR)] (where T = 2,5-disubstituted thiophene, R = CnH2n+1, n = 4, 6, 8, 12, 16). The blue monomers are preferred for the shorter chains (C4 and C6) and the violet compounds form exclusively for the longer chains (C8, C12, and C16) in the alkylthiophene complexes. In addition to the above series, [Ni(S2CTCH3)2], was prepared in a one-pot reaction in THF and both the blue and violet products were isolated. It was possible to convert the blue complexes [Ni(S2CTR)2] (R = butyl, hexyl) into the corresponding violet complexes [Ni(S2CTR)(S3CTR)] after stirring in THF solutions for prolonged periods of time. Liquid-crystalline properties of these complexes were examined by DSC and POM. The violet complexes with C8 and C12 alkyl chains showed liquid-crystalline properties. 相似文献
10.
The photoexcited triplet state of phenazine in toluene glasses at 35 K is investigated by light modulation-EPR spectroscopy. From the transient EPR spectra and the kinetics in the three canonical orientations (p = x, y, z) the rate parameters are determined. Thus, the depopulation rate constants kp, the anisotropic spin lattice relaxation rate constants Wp, and the ratios between the population constants Ap are calculated: kx = (2.2 ± 0.3) × 102 s?1, ky = (0.21 ± 0.04) × 102 s?1, kz = (0.06 ± 0.03) × 102 s?1, Wx = (8.6 ± 0.9) × 103 s?1, Wy = (11.0 ± 1.0) × 103 s?1, Wz = (14.0 ± 1.4) × 103 s?1, and Ax: Ay:Az ≈ 1:0.04:0.02. It is concluded therefore that the in-plane spin state |τx > is the active one. 相似文献