Tetragonal nanocrystals from the Zr0.5Ce0.5O2 solid solution by hydrothermal method

The formation of tetragonal Zr(0.5)Ce(0.5)O(2) solid solution nanocrystallites of 5 +/- 1 nm size by a hydrothermal method at 120 degrees C for 6 h was confirmed by careful Raman and XRD studies for the first time. It was characterized as the t' '-form with an axial ratio of c/a = 1 but with oxygen ion displacements. The as-prepared sample was hydrous in nature, which is responsible for the lattice expansion. However, most of the water held in the structure can be expelled by heating the sample above 600 degrees C. Above 1050 +/- 50 degrees C the t' '-form of tetragonal Zr(0.5)Ce(0.5)O(2) solid solution dissociates into two phases, cubic phase and the t-form of tetragonal phases.     

Template-directed DNA photoligation via alpha-5-cyanovinyldeoxyuridine

[reaction: see text] We describe an efficient template-directed photoligation of oligodeoxynucleotides (ODNs) using alpha-5-cyanovinyldeoxyuridine (alpha(C)U). An efficient photoligation was produced by photoirradiation of an ODN containing alpha(C)U at the 3' end with an ODN containing thymine at the 5' end in the presence of a template ODN. This photoligation method is a new and efficient way to synthesize branched ODNs.     

A new glycosylation method part 3: study of microwave effects at low temperatures to control reaction pathways and reduce byproducts

The efficiency of microwave irradiation at low temperature for glycosylations is described. Although oligosaccharide synthesis usually requires reactive donors for glycosylations, which have leaving groups on the anomer positions, i.e., trichloroacetoimidates, halogenates, thioalkyl glycosides, etc., the suitable donors in our microwave supported synthesis of Lewis X oligosaccharide were very stable acetate derivatives. Regarding glycosylation with a fucosyl acetate donor and a glucosamine acceptor, microwave irradiation with simultaneous cooling improved yields. Moreover, further synthesis to Lewis X derivatives was achieved only with microwave irradiation at low temperatures. Without microwave irradiation, we could only obtain byproducts and none of the designed product at any reaction temperature.     

Comparison of pharmacological effects of tetrahydrocannabinols and their 11-hydroxy-metabolites in mice

Pharmacological effects (catalepsy, hypothermia, pentobarbital-induced sleep prolongation, anticonvulsant and analgesic effects) of delta 8- and delta 9-tetrahydrocannabinols, and their 11-hydroxy-metabolites were evaluated and compared in mice. delta 9-Tetrahydrocannabinol and 11-hydroxy-delta 9-tetrahydrocannabinol exhibited somewhat greater effects than did delta 8-tetrahydrocannabinol and 11-hydroxy-delta 8-tetrahydrocannabinol, respectively, in all pharmacological indices tested. Greater effects of 11-hydroxy-metabolites than those of tetrahydrocannabinols were also demonstrated.     

Discontinuous boundary implementation for the shallow water equations

Quasi‐bubble finite element approximations to the shallow water equations are investigated focusing on implementations of the surface elevation boundary condition. We first demonstrate by numerical results that the conventional implementation of the boundary condition degrades the accuracy of the velocity solution. It is also shown that the degraded velocity leads to a critical instability if the advection term is present in the momentum equation. Then we propose an alternative implementation for the boundary condition. We refer to this alternative implementation as a discontinuous boundary (DB) implementation because it introduces at each boundary node two independent mass–flux values that result in a discontinuity at the boundary. Numerical results show that the proposed DB implementation is consistent, stabilizes the quasi‐bubble scheme, and leads to second‐order accuracy at the surface elevation specified boundary. Copyright © 2004 John Wiley & Sons, Ltd.