Search results for "Crystal"

Spin-Transition in [Fe(II)(2,6-Bis-(Benzimidazol-2′-yl)pyridine)2] (CIO4)2: Hysteresis Effect Dependent on the Matrix

1999

Abstract Far-Infrared spectroscopical investigation of the spin-crossover in [Fe(II)(2,6-bis-(benzimidazol-2′-yl)-pyridine)2] (CIO4)2 exhibits a hysteresis in both CsI and polyethylene matrices within temperature cycles between 100K and 520K. The hysteresis broadening is dependent on the matrix and bigger in CsI. This can be explained due to polarity and hydrogen bonding. Two low spin vibrations, LS1 at 437 cm−1 and LS2 at 424cm−1, are observed. On heating from 100K to 520K: during LS1 decreases, the LS2 raises temporarily, until both LS1 and LS2 disappear; for the HS only one raising species was observed. This gives raise to assume two different sub-lattices.

Influence of a hydrophilic spacer on the structure of a phospholipid monolayer

1994

We present the results of thermodynamical and X-ray grazing incidence diffraction experiments performed on Langmuir monolayers of ether lipids with hydrophilic spacers between the glycerol backbone and the phosphatidylcholine head group: DHPC, DH-E01-PC, and DH-E02-PC. As a spacer the oxy-ethylene group is used, which is a typical hydrophilic unit of non-ionic tensides. It turns out that the introduction of the hydrophilic spacers leads to a fluidization of the monolayer and reduces the tilt angle of the chains.

Low-energy decay pathways of doubly charged silver clusters $Ag_{n}^{2+}$ (n = 9 - 24)

1997

The low-energy dissociation channels of mass selected silver cluster ions Ag n 2+ (n = 9–24) are determined by collision induced dissociation (CID) in a Penning trap. While all clusters of the size n ≥ 17 evaporate neutral monomers, most smaller clusters undergo asymmetric fission of the form Ag n 2+ → Ag −3 + + Ag {3} + . However, Ag 15 2+ and Ag 11 2+ emit monomers which indicates shell or odd-even effects. The observed fragmentation pathways are different from previous reports of measurements with sputtered Ag n 2+ .

Slow Relaxation of the Magnetization in a {Co <sup>III</sup>Mn <sup>III</sup>} Heterometallic Brick-Wall Network

2021

The use of the cyanide-bearing dicobalt(III) complex (PPh 4 ) 2 [Co 2 III (m-2,5-dpp)(CN) 8 ] as a metalloligand towards [Mn(salen)(H 2 O)]ClO 4 afforded the heterobimetallic two-dimensional compound of formula [{Mn III (salen)} 2 {(m-NC) 4 Co 2 III (m-2,5-dpp)(CN) 4 }] n (1) [PPh 4 + = teraphenylphosphonium cation, 2,5-dpp = 2,5-bis(2-pyridyl)pyrazine and H 2 salen = N,N’ -ethylenebis(salicylideneimine)] whose structure has been determined by single crystal X-ray diffraction. Compound 1 exhibits a neutral brick-wall structure, where each [Co 2 III (m-2,5-dpp)(CN) 8 ] 2- unit adopts a tetrakis-monodentate bridging mode towards four {Mn III (salen)} + fragments through four of its eight cyan…

Titelbild: Cyanide-Bridged Iron(III)–Cobalt(II) Double Zigzag Ferromagnetic Chains: Two New Molecular Magnetic Nanowires (Angew. Chem. 13/2003)

2003

A remark on the surface structure of polyethylene single crystals

1967

IR Spectroscopy of Monoclinic Tungsten Oxide

2000

Stoichiometric tungsten trioxide WO3 has several polimorphous crystal phases [1] in the temperature region from 4 up to 1200K. These WO3 phases have more or less distorted ReO3 — type crystal structures, and ReO3 lattice topology is identical to topology of the BO3 sublattice of perovskite ABO3.

Inside Back Cover: N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates (Ange…

2020

ChemInform Abstract: 4,4,4′,4′,7,7′-Hexamethyl-2,2′-spirobichroman.

2010

The title compound, C23H28O2, was obtained from the reaction of acetone with meta-cresol. The molecular structure consists of two identical subunits which are nearly perpendicular to each other. The oxygen-containing rings are not planar and the molecule is chiral. The crystal structure consists of chains of molecules of the same chirality arranged along the [010] axis.

Syntheses, crystal structures and magnetic properties of polynuclear 1,4,5,8,9,12-hexaazatriphenylene (hat)-bridged copper(II) complexes

2001

Three polynuclear compounds containing copper(II) and 1,4,5,8,9,12-hexaazatriphenylene (hat) as the basic building blocks have been prepared, [Cu4(hat)2Cl8]n·6nH2O 1, [Cu(hat)(H2O)2]n[NO3]2n2, and [Cu2(hat)(H2O)6]n[SO4]2n·2nH2O 3, their crystal structures determined and variable-temperature magnetic susceptibility data measured. The basic building block in 1 is the dinuclear [Cu2(hat)Cl4] entity, two such units being connected to tetranuclear units through relatively strong axial Cu–Cl bonds (out-of-plane di-μ-chloro bridges). Weaker axial Cu⋯Cl interactions link the units into a sheet structure. In 2 and 3 hat-bridged copper(II) chains extending along glide planes are present. hat serves a…