Octahedral Symmetry (octahedral + symmetry)

Distribution by Scientific Domains


Selected Abstracts


Layered [BaM(C3H2O4)2(H2O)4] (M = Fe or Co) Complexes , Spectroscopic, Magnetic and Thermal Study

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 16 2003
Izaskun Gil de Muro
Abstract Complexes with formula [BaM(C3H2O4)2(H2O)4], where M = Fe or Co, were synthesised and characterised. These two types of complexes are isostructural and crystallise in the Pccn space group. Their structure consists of two-dimensional networks of octahedral MO6 polyhedra in which the transition metal ions are coordinated by bridging malonate ligands, through the O-C-O atoms. These M-malonate units are extended along the crystallographic [101] plane. Spectroscopic data are consistent with the cations being in a high-spin octahedral symmetry. The two types of compounds exhibit 2D antiferromagnetic interactions as well as weak ferromagnetism below the Néel temperature, as a result of an intralayer misalignment of the spins. Thermal treatment of the metallo-organic precursors gave rise to BaMO3,y oxides at lower temperatures and reaction times than those found in the literature using the ceramic method. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003). [source]


Application of the anharmonic coherent states to the vibronic interaction

FORTSCHRITTE DER PHYSIK/PROGRESS OF PHYSICS, Issue 2-3 2003
C.N. Avram
We calculated the vibronic reduction factor (Ham factor) for the physical system (molecules, crystals) with octahedral symmetry. The vibrations of the nuclei of the systems are described by the anharmonic states of the Morse potential and also by the anharmonic coherent states of the same potential. The linear vibronic coupling of these vibration states with the electronic states of the system are considered. [source]


Symmetry and bifurcation in vestibular system

PROCEEDINGS IN APPLIED MATHEMATICS & MECHANICS, Issue 1 2007
Marty Golubitsky
The vestibular system in almost all vertebrates, humans included, controls balance by employing a set of six semicircular canals, three in each inner ear, to detect angular accelerations of the head. Signals from the canals are transmitted to neck motoneurons and activate eight corresponding muscle groups. These signals may be either excitatory or inhibitory, depending on the direction of acceleration. McCollum and Boyle have observed that in the cat the network of neurons concerned possesses octahedral symmetry, a structure deduced from the known innervation patterns (connections) from canals to muscles. We re-derive the octahedral symmetry from mathematical features of the probable network architecture, and model the movement of the head in response to the activation patterns of the muscles concerned. We assume that connections among neck muscles can be modeled by a ,coupled cell network', a system of coupled ODEs whose variables correspond to the eight muscles, and that network also has octahedral symmetry. The network and its symmetries imply that these ODEs must be equivariant under a suitable action of the octahedral group. Using results of Ashwin and Podvigina, we show that with the appropriate group actions, there are six possible spatiotemporal patterns of time-periodic states that can arise by Hopf bifurcation from an equilibrium corresponding to natural head motions. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Synthesis, Structure and Characterization of Two-dimensional Network Copper Complex [Cu3(nta)2(azpy)2(H2O)2]·6H2O

CHINESE JOURNAL OF CHEMISTRY, Issue 2 2002
Bao-Long Li
Abstract The copper(II) complex[Cu3(nta)2(azpy)2(H2O)2]·6H2O (nta = nitrilotriacetate, azpy = 4,4,-azobispyridine) has been synthesized and characterized. The X-ray analysis reveals that there are two kinds of copper(II) coordination environments. Cu(1) has a distorted square plane symmetry and Cu(2) has a distorted octahedral symmetry. Cu(1) is linked to Cu(2) through nta and bound to Cu(1C) by azpy, and Cu(2) is linked to Cu(2A) through azpy, which extends to two-dimensional network with large rhombus 1.2 nm × 1.7 nm. [source]