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61.
The confinement of a nonneutral plasma in a magnetic-surface, or stellarator, configuration is explored. The fluid equilibrium equations are derived and are found to be fundamentally different from previous results. Diocotron modes are predicted to be stable. The collisional confinement time can be very long. Possible applications include positron trapping and confinement of positron-electron plasmas. The basic physics can be addressed experimentally in the simple tabletop stellarator planned for construction at Columbia University.  相似文献   
62.
We propose a theoretical model for the recently reported anomalously long decay of a space-charge field that was resonantly excited in a photorefractive sillenite crystal [Phys. Rev. Lett. 79, 67 (1997)]. The model is based on the conventional concept of charge transfer and does not require excessively large values of the quality factor for space-charge waves. The effect in question is qualified as a critical slowing of the relaxation process as the threshold of optical oscillation is approached.  相似文献   
63.
64.
For an arbitrary separable locally compact group G we exhibit a canonical Borel subset G?Δ of the quasi-dual G?of G (with the Mackey Borel structure), such that G?Δ is a standard Borel space in the induced Borel structure, and such that the canonical measure for the left regular representation λGof G is concentrated on G?Δ. On the basis of this we discuss the (non-unimodular) “Plancherel theorem.”  相似文献   
65.
66.
The microwave spectrum of MnO3F has been remeasured and several corrections and new results have been obtained: B0 = 4129.141 MHz, DJ = 1.12 kHz, DJK = 1.87 kHz; α3B = 8.622, α5B = ? 11.994, α6B = 6.042, |q5| = 16.005, and |q6| = 8.456 MHz.  相似文献   
67.
Ab initio calculations at the STO—3G level have been performed on the binding of CA(II) ion to malonate and formate with and without d orbitals in the basis set for the CA(II) ion. The malonate and formate binding results with CA(II) are similar. The addition of d orbitals to CA(II) has little effect on the conformational minimum. The results are qualitatively similar to those from our previous calculations on the Mg2+—malonate interaction: a single carboxyl interaction with the metal ion appears to be preferred over a conformation in which two carboxyl groups bind to Ca(II). Moreover, the single carboxyl group interaction with CA(II) appears to be favored over the binding of CA(II) to a single oxygen of a carboxyl group.  相似文献   
68.
Dispersion limits performance in many optical systems. In surface plasmon resonance (SPR) biosensors, the sensing area is an optical element in which the dispersion depends on the effective refractive index of the biochemical compounds to be measured. We report a method of compensating for wavelength dispersion in SPR biosensors employing two integrated diffractive optical coupling elements in a polymer substrate. The dispersion compensation is achieved over the whole dynamic measurement range and provides a biosensor more robust to wavelength fluctuations than prism-coupler SPR systems. The concept can readily be employed in other types of sensor measuring refractive-index changes.  相似文献   
69.
The energy-resolved rate coefficient for the dissociative recombination (DR) of H(3)(+) with slow electrons has been measured by the storage-ring method using an ion beam produced from a radiofrequency multipole ion trap, employing buffer-gas cooling at 13 K. The electron energy spread of the merged-beams measurement is reduced to 500 microeV by using a cryogenic GaAs photocathode. This and a previous cold- measurement jointly confirm the capability of ion storage rings, with suitable ion sources, to store and investigate H(3)(+) in the two lowest, (J,G) = (1,1) and (1,0) rotational states prevailing also in cold interstellar matter. The use of para-H(2) in the ion source, expected to enhance para-H(3)(+) in the stored ion beam, is found to increase the DR rate coefficient at meV electron energies.  相似文献   
70.
[reaction: see text] The organometallic intermediate obtained from halogen-metal exchanges of 4-iodo-6-phenylthieno[2,3-d]pyrimidine under Barbier-type conditions was reacted with aldehydes to form the corresponding alcohols in moderate yields. The reaction involving an organolithium intermediate proceeded only at low temperature, whereas the reaction involving a magnesium ate intermediate also proceeded at room temperature. A crystal structure confirms that the expected constitutional alcohol isomer is formed, where no migration has taken place. The conditions were also suitable for 9-benzyl-6-iodopurine.  相似文献   
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