Descripción: Two copper complex solvatomorphs, namely (3,10-C-meso-3,5,7,7,10,12,14,14- octamethyl-1,4,8,11-tetraazacyclotetradecane)bis(perchlorato-κO)copper(II) 1.2-hydrate, [Cu(ClO4)2(C18H 40N4)]·1.2H2O, (I), and (3,10-C-meso-3,5,7,7,10,12,14,14-octamethyl-1,4,8,11-tetraazacyclotetradecane) bis(perchlorato-κO)copper(II), [Cu(ClO4)2(C 18H40N4)], (II), are described and compared with each other and with a third, already reported, anhydrous diastereomer, denoted (III). Both compounds present very similar centrosymmetic coordination environments, with the CuII cation lying on an inversion centre in a distorted 4+2 octahedral environment, defined by the macrocyclic N4 group in the equatorial sites and two perchlorate groups in trans-axial positions [one of the perchlorate ligands in (I) is partially disordered]. The most significant difference in molecular shape is seen in the orientation of the perchlorate anions, and the influence of this on the intramolecular hydrogen bonding is discussed. The (partially) hydrated state of (I) favours the formation of chains along [011], while the anhydrous character of (II) and (III) promotes loosely bound structures with low packing indices. © 2013 International Union of Crystallography.

Descripción: The title compound, tetrakis(μ-3,4,5-triethoxybenzoato κ 2 O:O′)bis[(pyrazine-κN)rhodium(II)](Rh-Rh). [Rh 2 (C 13 -H 17 O 5 ) 4 (C 4 H 4 N 2 ) 2 ], crystallizes on an inversion centre in the triclinic space group P1̄. The equatorial carboxylate ligands bridge the two Rh 11 atoms, giving a binuclear lantern-like structure. The pyrazine molecules occupy the two axial coordination sites. The phenyl rings are titled by ca 10° with respect to the attached carboxylate groups. The pyrazine planes have a torsion angle of ca 19° around the Rh-N bond with respect to the plane of the nearer carboxylate group and are not coplanar with the Rh-Rh bond.

Descripción: The Kelvin-Helmoltz instability (KH) with formation of vortices appears in a wide variety of terrestrial, interplanetary, and astrophysical contexts. We study a series of iterated rolled-up coherent plasma structures (15) that flow in the equatorial Earth's boundary layer (BL), observed on October 24, 2001. The data were recorded during a 1.5 hour-long Wind crossing of the BL at the dawn magnetospheric flank, tailward of the terminator (X≈-13 RE). The interplanetary magnetic field (IMF) was radially directed, almost antiparallel to the magnetosheath (MS) flow. This configuration is expected to be adverse to the KH instability because of the collinearity of field and flow, and the high compressibility of the MS. We analyze the BL stability with compressible MHD theory using continuous profiles for the physical quantities. Upstream, at near Earth sites, we input parameters derived from an exact MHD solution for collinear flows. Further downtail at Wind position we input measured parameters. The BL is found KH unstable in spite of unfavorable features of the external flow. On the experimental side, the passage of vortices is inferred from the presence of low density - hot plasma being accelerated to speeds higher than that of the contiguous MS. It is further supported by the peculiar correlation of relative motions (in the bulk velocity frame): cold-dense plasma drifts sunward, while hot-tenuous plasma moves tailward. This event differs from many other studies that reported BL vortices under strongly northward IMF orientations. This is a case of KH vortices observed under an almost radial IMF, with implicit significance for the more common Parker's spiral fields, and the problem of plasma entry in the magnetosphere.

Descripción: The three transition-metal complexes, (meso-5,7,7,12,14,14-hexa methyl-1,4,8,11-tetra azacyclo tetra decane-κ4 N)bis (perchlorato-κO)copper(II), [Cu(ClO4)2(C18H40N4)], (I), (meso-5,7,7,12,14,14-hexa methyl-1,4,8,11-tetra azacyclo tetra decane-κ4 N)bis (nitrato-κO)zinc(II), [Zn(NO3)2(C18H40N4)], (II), and aqua chlorido (meso-5,7,7,12,14,14-hexa methyl-1,4,8,11-tetraazacyclo tetra decane-κ4 N)copper(II) chloride, [CuCl(C18H40N4)(H2O)]Cl, (III), are described. The mol ecules display a very similarly distorted 4+2 octa hedral environment for the cation [located at an inversion centre in (I) and (II)], defined by the macrocycle N4 group in the equatorial sites and two further ligands in trans-axial positions [two O-ClO3 ligands in (I), two O-NO2 ligands in (II) and one chloride and one aqua ligand in (III)]. The most significant difference in mol ecular shape resides in these axial ligands, the effect of which on the intra- and inter molecular hydrogen bonding is discussed. In the case of (I), all strong hydrogen-bond donors are saturated in intra molecular inter actions, while weak inter molecular C - H⋯O contacts result in a three-dimensional network. In (II) and (III), instead, there are N - H and O - H donors left over for inter molecular inter actions, giving rise to the formation of strongly linked but weakly inter acting chains. © 2013 International Union of Crystallography.