Thermal expansion in (La0.62Pb0.38)MnO3: Possible evidence for a coupling between elastic and magnetic exchange forces

Using single-crystal, automated diffractometer techniques, the linear coefficient of thermal expansion has been determined for La_0.62Pb_0.38MnO₃ from 298 to 627 K. The linear coefficient of thermal expansion is observed to undergo a change from 7.2 × 10^?5 Å/K for T < T_c to 10.8 × 10^?5 Å/K for T > T_c. It is concluded that while the rhombohedral distortion in the (La, Pb)MnO₃ system can be understood qualitatively on the basis of ionic size and polarizability considerations alone, the quantitative systematics of the distortion parameters and the change in the linear thermal expansion coefficient at T_c indicate a significant coupling between the elastic and magnetic exchange forces.     

A weight-function approach for determining watershed initial conditions for combustion waves

In many generic combustion models, one finds that a combustionwave will develop with a specific wave speed. However, thereare possible initial temperature profiles which do not evolveinto such waves, but rather die out to the ambient temperature.There can exist, in some models, a clear distinction betweenthose initial conditions that do evolve into combustion wavesand those that do not; this is sometimes referred to as thewatershed initial condition. When fuel consumption is consideredto be negligible, analytical methods can be used to obtain theexact watershed. In this paper, we consider the problem of determiningpseudo-watersheds and ascertaining the relationship betweenthese pseudo-watersheds and the exact watersheds. In the processa novel weight-function approach for infinite spatial domainsis developed.     

Synthesis of cytotoxic cyanobactin,Wewakazole B

We report herein the synthesis of cytotoxic cyanobactin, Wewakazole B through an efficient solution-phase approach. The key steps of the synthesis are the macrocyclic lactamization of linear dodecapeptide and construction of two hexapeptides with three different substituted oxazole rings.     

Crystal structure of naturally occurring mercury(II) amidonitrate

A naturally-occurring mercuroammonium compound from Pitkin County, Colorado, is shown to be the natural analog of synthetic HgNH₂NO₃. The crystals are isometric, P4₁32 or P4₃32, with a = 10.254(1)Å and twelve formula weights per cell. Using 437 symmetry-independent reflections, the crystal structure was partially determined and refined to a residual of 0.090. The positions of the Hg atoms and the N and O atoms of the nitrate group were determined, but the amide ion could not be located, probably due to positional disorder. The structure contains mercury atoms arranged in equilateral triangles 3.421(1) Å on a side. These triangles are linked through shared vertices into helical chains wound around the fourfold screw axes. Similar triangular units occur in other inorganic Hg(II) compounds. The distortion of the nitrate ion from trigonal planar symmetry is also discussed.