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71.
Janet Whalen Kammeyer 《Journal d'Analyse Mathématique》1990,54(1):113-163
A theorem is proven which gives five characterizations of a multidimensional Bernoulli shift. The two-point extensions of
a multidimensional Bernoulli shift are classified completely. If such an extension is weakly mixing then it must be Bernoulli;
otherwise, it is isomorphic to one of 2
n
specific trivial extensions. This result is extended to multidimensional Bernoulli flows and Bernoulli shifts of infinite
entropy.
This work supported in part by N.S.F. Grant DMS-85-04701 and by the University of Maryland Department of Mathematics. 相似文献
72.
Neutron total cross sections of 6Li are measured at intervals of ? 10 keV from ≈ 0.1 to 4.8 MeV with precisions of ≈ 1 to 3 %. Differential elastic scattering cross sections are measured at intervals of ? 100 keV from 1.5 to 4.0 MeV at 10 or more scattering angles distributed between ≈ 20 and 160 deg. Differential inelastic scattering cross sections are measured at selected angles in the energy range 3.5 to 4.0 MeV. The experimental results are analyzed in terms of R-matrix theory and the model parameters used to deduce the cross sections. The implications of the measurements and their interpretation on the level structure of 7Li and the reaction mechanisms are discussed. 相似文献
73.
The salt, [F5TeN(H)Xe][AsF6], has been synthesized in the natural abundance and 99.5% 15N-enriched forms. The F5TeN(H)Xe+ cation has been obtained as the product of the reactions of [F5TeNH3][AsF6] with XeF2 (HF and BrF5 solvents) and F5TeNH2 with [XeF][AsF6] (HF solvent) and characterized in solution by 129Xe, 19F, 125Te, 1H, and 15N NMR spectroscopy at -60 to -30 degrees C. The orange [F5TeN(H)Xe][AsF6] and colorless [F5TeNH3][AsF6] salts were crystallized as a mixture from HF solvent at -35 degrees C and were characterized by Raman spectroscopy at -165 degrees C and by X-ray crystallography. The crystal structure of the low-temperature phase, alpha-F5TeNH2, was obtained by crystallization from liquid SO2 between -50 and -70 degrees C and is fully ordered. The high-temperature phase, beta-F5TeNH2, was obtained by sublimation at room temperature and exhibits a 6-fold disorder. Decomposition of [F5TeN(H)Xe][AsF6] in the solid state was rapid above -30 degrees C. The decomposition of F5TeN(H)Xe+ in HF and BrF5 solution at -33 degrees C proceeded by fluorination at nitrogen to give F5TeNF2 and Xe gas. Electronic structure calculations at the Hartree-Fock and local density-functional theory levels were used to calculate the gas-phase geometries, charges, Mayer bond orders, and Mayer valencies of F5TeNH2, F5TeNH3+, F5TeN(H)Xe+, [F5TeN(H)Xe][AsF6], F5TeNF2, and F5TeN2- and to assign their experimental vibrational frequencies. The F5TeN(H)Xe+ and the ion pair, [F5TeN(H)Xe][AsF6], systems were also calculated at the MP2 and gradient-corrected (B3LYP) levels. 相似文献
74.
Sugiyama M Hong Z Liang PH Dean SM Whalen LJ Greenberg WA Wong CH 《Journal of the American Chemical Society》2007,129(47):14811-14817
A one-pot chemoenzymatic method for the synthesis of a variety of new iminocyclitols from readily available, non-phosphorylated donor substrates has been developed. The method utilizes the recently discovered fructose-6-phosphate aldolase (FSA), which is functionally distinct from known aldolases in its tolerance of different donor substrates as well as acceptor substrates. Kinetic studies were performed with dihydroxyacetone (DHA), the presumed endogenous substrate for FSA, as well as hydroxy acetone (HA) and 1-hydroxy-2-butanone (HB) as donor substrates, in each case using glyceraldehyde-3-phosphate as acceptor substrate. Remarkably, FSA used the three donor substrates with equal efficiency, with kcat/KMvalues of 33, 75, and 20 M-1 s-1, respectively. This level of donor substrate tolerance is unprecedented for an aldolase. Furthermore, DHA, HA, and HB were accepted as donors in FSA-catalyzed aldol reactions with a variety of azido- and Cbz-amino aldehyde acceptors. The broad substrate tolerance of FSA and the ability to circumvent the need for phosphorylated substrates allowed for one-pot synthesis of a number of known and novel iminocyclitols in good yields, and in a very concise fashion. New iminocyclitols were assayed as inhibitors against a panel of glycosidases. Compounds 15 and 16 were specific alpha-mannosidase inhibitors, and 24 and 26 were potent and selective inhibitors of beta-N-acetylglucosaminidases in the submicromolar range. Facile access to these compounds makes them attractive core structures for further inhibitor optimization. 相似文献
75.