Search results for "Ferro"

Blends from redox active liquid crystal ionomers and amorphous ionomers

1994

Abstract Biphasic blends (mixtures) of liquid crystal ionomers (prepared from ferrocene containing liquid crystal polymers by a redox reaction) and partially sulfonated polystyrene combine the constituent properties in a way, which is dependent on the measuring method. Polarizing microscopy shows homogenous textures similar to the pure liquid crystal polymer. Mechanical measurements show however the elastomeric behaviour of sulfonated polystyrene. The phase separated structure of these blends is proved by differential scanning calorimetry measurements.

Cellulose-click-ferrocenes as docking spots for cyclodextrin

2012

A novel synthesis of ferrocene-modified cellulose, prepared from 6-azido-6-deoxy-cellulose and ethynylferrocene, is presented. The two components were coupled via copper-catalyzed click-type cycloaddition under microwave-assisted conditions. The surface structure of the cellulose derivative was investigated in comparison with that of pure, microcrystalline cellulose using electron microscopy (scanning, transmission and scanning transmission), showing iron atoms of ferrocene as homogeneously distributed particles. They are detectable as clear signals in the energy-dispersive X-ray profile. In addition, Rame-β-cyclodextrin was supramolecularly attached to cellulose and the complex formed was …

Ferroelectric block copolymers

1997

A block copolymer consisting of polystyrene and a side chain ferroelectric liquid crystalline polymer was synthesized using polymer analogous chemistry on a monodisperse poly(styrene-b-isoprene). Composition was adjusted to give lamellar microstructure after addition of the mesogenic side groups. If placed in an LC cell without orientation of domains, no ferroelectric response was observed. After shearing the thin film, presumably due to alignment of lamellae, a bistable ferroelectric switching could be detected.

Ferroelectric LC-elastomers

1997

Ferroelectric liquid crystalline elastomers combine the rubber elasticity of polymer networks with liquid crystalline phases and ferroelectric ordering. Ferroelectric switching leads therefore to a deformation of the polymer network and an elastic stress. The coupling between both effccts can be varied by changing the topology of the netpoints.

1996

Combined LC-polymers possess the structural properties of both LC main chain and LC side chain polymers. Beneath this structural speciality, their broad LC-phases and their polymorphism (different smectic phases and one nematic phase as a function of temperature) make them interesting. Crucial to an understanding of them is the fact that main chain and side chain mesogens orient parallel to each other and interact cooperatively to form the LC-phase. Due to this synergism the temperature range of the LC-phase is much broader than that of the corresponding LC main chain and LC side chain polymers. This interplay of main chain and side chain mesogens allows structures to be designed with prefe…

Visible polarized light transmission spectroscopy of the electro-optic switching behaviour of surface stabilized ferroelectric liquid crystal cells

1991

Abstract We present in this paper an experimental and theoretical modelling study of the switching characteristics and electro-optic behaviour of chevron surface stabilized ferroelectric liquid crystal cells with planar (low pre-tilt) and non-planar (high pre-tilt) surface conditions. The visible polarized light transmission spectra were taken of the cells with glass plates coated with films of either rubbed polymer or obliquely evaporated silicon monoxide (SiO) at various applied voltages and in various stages of switching and compared with the theoretical values calculated numerically based on our director-polarization structure model for the aforementioned cells. The results provide evid…

Assembling Magnetic Blocks: A Strategy to Control the Nuclearity and Magnetic Properties of Polynuclear Complexes

1996

Synthetic strategies dealing with the polymerization of either di-μ-hydroxocopper(II) complexes or 2,2′-bipyrimidine (bpym)-containing first row transition metal ions allow the preparation of polynuclear compounds whose structures and magnetic properties are presented here. The influence of structural and chemical parameters on the magnitude of the singlet-triplet energy gap (J) in di-μ-hydroxocopper(II) complexes [LCu(OH)2CuL]2+ with L = 2,2′-bipyridine (bpy) and bpym is analyzed and discussed. Special attention is devoted to nature of the counterion which allows the preparation of hydroxo-bridge copper(II) cubane and double cubane type complexes where all the intramolecular magnetic inter…

Experimental and Theoretical Study of Dynamic Structural Transformations between Sensing Copper(II)-Uracil Antiferromagnetic and Metamagnetic Coordin…

2020

This paper describes the synthesis and characterization of several Copper(II)-uracil-1-propionic acid (UPrOH) coordination compounds, including the theoretical and experimental study of their cryst...

Expanding the 3d-4f heterometallic chemistry of the (py)2CO and pyCOpyCOpy ligands: structural, magnetic and Mössbauer spectroscopic studies of two F…

2011

Complex [Fe(II)Gd(III){pyCO(OEt)pyCOH(OEt)py}(3)](ClO(4))(2) (1) crystallizes in the Cc space group and contains one hexacoordinate ferrous ion and one enneacoordinate Gd(III) ion. Complex [Fe(2)(II)Gd(III){pyCO(OEt)py}(4)(NO(3))(H(2)O)][Gd(NO(3))(5)](0.5)(ClO(4)) (2) crystallizes in the C2/c space group and contains two hexacoordinate ferrous ions and one octacoordinate Gd(III) ion. Both complexes have been prepared by the metal-assisted ethanolysis of ligands di-2,6-(2-pyridylcarbonyl)pyridine (pyCOpyCOpy, dpcp) and di-2-pyridyl ketone ((py)(2)CO, dpk), which exhibit similar structures. Mössbauer spectroscopic studies of 2 revealed the presence of two quadrupole-split doublets of equal in…

Dimesogenic liquid crystalline oligosiloxanes

1995

Abstract In this paper, the syntheses, phase properties and ferroelectric properties of new liquid crystalline oligosiloxane dimesogens are described. Smectic phases are dominant in this class of materials. Spontaneous polarizations are in the range of 10 to approximately 100 nCcm−2. The materials show interesting properties for display applications. Although offering higher mechanical stability than low molar mass materials, their switching is significantly faster (switching times in the range of some 10−5s) than is the case for similar side group polymers (typically some 10−3s). Therefore these new oligosiloxane derivatives may be ideal for building flexible displays. In addition, mixture…