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21.
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Christoph Meingast Frank Gugenberger Georg Roth Miro Haluška Hans Kuzmany 《Zeitschrift für Physik B Condensed Matter》1994,95(1):67-71
The thermal expansion of vapor-grownC
70 single crystals ahs been investigated using high-resolution capacitance dilatometry from 5–380 K. Measurements were made both parallel and perpendicular to the hexagonalc-axis. Three first-order phase transitions which we associate with the consecutive disordering of theC
70 molecules are observed upon heating at 280 K (long-axis spinning), 300 K (long-axis precession) and 355 K (quasi-free rotation), respectively. The highest-temperature transition exhibits a very large (50 K) thermal hysteresis. Powder and single-crystal X-ray diffraction show that the crystals are predominantly hexagonal-close-packed (HCP) with an idealc/a1.63 above 360 K andc/a1.84 at 295 K. 相似文献
23.
Continuing the recent work of the second author, we prove that the diophantine equation
for has exactly 12 solutions except when , when it has 16 solutions. If denotes one of the zeros of , then for we also find all with .
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25.
Ron M. Roth 《Designs, Codes and Cryptography》1996,9(2):177-191
Codes
of length 2
m
over {1, -1} are defined as null spaces of certain submatrices of Hadamard matrices. It is shown that the codewords of
all have an rth order spectral null at zero frequency. Establishing the connection between
and the parity-check matrix of Reed-Muller codes, the minimum distance of
is obtained along with upper bounds on the redundancy of
. An efficient algorithm is presented for encoding unconstrained binary sequences into
. 相似文献
26.
S. E. Arnell D. Foltescu H. A. Roth Ö. Skeppstedt A. Nilsson S. Mitarai J. Nyberg 《Zeitschrift für Physik A Hadrons and Nuclei》1993,346(2):111-117
The level structure of92Ru has been studied by means of γ-ray spectroscopy. The nucleus was produced by the58Ni(40Ca, α2p)92Ru reaction at beam energies of 147 and 187 MeV. The NORDBALL detector system including particle selection was used. A large number of new levels with excitation energies up to 11.3 MeV and spin values up to 22 or 23 units of angular momentum have been established. The level scheme is compared with recent shell model calculations using100Sn as a core. Some systematics of the g 9 2/?2 configuration is discussed and a strong correlation between the levels in90Mo and92Ru is found. 相似文献
27.
H. J. Byrne L. Akselrod C. Thomsen A. Mittelbach S. Roth 《Applied Physics A: Materials Science & Processing》1993,57(4):299-302
The resonant Raman scattering of C60 crystallites is monitored as a function of excitation intensity at 514.5 nm. At low intensities, a strong line at 1468 cm–1 is observed. No feature at 1459 cm–1 is observable. With increasing intensities, the 1468 cm–1 line shifts continuously and reversibly to lower frequencies. The mode softening is nonlinearly dependent on the input intensity and is accompanied by a nonlinear increase in the Raman intensity. The spectral changes are discussed in terms of a nonlinear reduction in force constant and increase in bond polarisability as a result of an increased intermolecular delocalisation of the -electron cloud. The nonlinear changes are associated with the nonlinear luminescence and photoconductive response observed in fullerenes and are contrasted to the irreversible phototransformation recently discussed. 相似文献
28.
Five acidic calix[4]arenes with carboxylic or sulfonic groups at either the upper or lower rim of the cavity and one resorc[4]arene were investigated to separate three thioxanthenes (flupentixol, clopenthixol, chlorprothixene) and a dibenz[b,e]oxepin derivative (doxepin) with cis-/trans-isomerism by nonaqueous capillary electrophoresis (NACE). Partial filling of the capillary with the UV-absorbing selectors led to a low detection limit and an advantageous signal-to-noise ratio (S/N). A sufficient electrophoretic mobility of the calixarenes towards the anode was necessary to outweigh the oppositely directed electroosmotic flow (EOF). This depended from the functional groups, the dissociation and the hydrodynamic radius of the cyclophanes. In contrast, the resorcinarene was useable only by addition of sodium dodecyl sulfate (SDS) because only the complex of the two selectors had an anodic apparent electrophoretic mobility. p-Sulfonyl-calix[4]arene (ss-a1) was the most capable selector for all E/Z-isomers with maximal alpha-values ranging from 1.056 for doxepin to 1.224 for chlorprothixene. This was due to the sufficient migration in reversed direction to the EOF even at low pH* values of 3.0. Otherwise, electrostatic as well as hydrophobic interactions with the positively charged isomers seem to contribute to a superior recognition. Increasing the concentration up to 15 mM ss-a1 and using acidic media (pH* 5.0) led to high separation efficiency. Changing the organic solvent provides a powerful tool to improve selectivity with N,N-dimethylformamide-methanol (DMF-MeOH)-mixtures for thioxanthenes. Further electrophoretic parameters were optimized, such as the concentration of the electrolytes, the addition of SDS, the kind of electrolytes and the voltage. Distinct differences in selectivities were found between the derivatives with thioxanthene and dibenzo[b,e]oxepin ring system, respectively. Further, the different basic side chain was responsible for the different selectivity at higher pH* values. In contrast, the substitution at position 2 of the thioxanthenes played a secondary role. Based on the studies of single parameters a method for a simultaneous separation of the four pairs of isomers within 13 min was developed. 相似文献
29.
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