Search results for "PHENYLENE"

1983

The first dissociation constant of oligonuclear phenolic compounds consisting of one nitrophenol unit besides further alkyl phenol units (10 dinuclear, 15 trinuclear, 6 tetranuclear compounds, and 4 nitrophenols as model) was determined spectroscopically in water/methanol (50/50 by vol.) at 25°C. For the ortho-linked title compounds with the nitrophenol unit at the end of the molecule a decrease of pK1 is observed which becomes stronger with increasing chain length. The introduction of bulky groups in ortho-position of the dissociating phenolic unit, as well as at the opposite end of the molecule causes a further decrease of pK1. The lowest value is found for a p-nitrophenol unit in the mid…

Neue extrem deformierte (Biphenylen‐)Kohlenwasserstoff‐Gerüste

1992

New Extremely Deformed (Biphenylene)Hydrocarbon Skeletons The tetracyclic carbon skeleton 2-oxo[3](1,8)biphenylenophane (4) was synthesized by cyclization of a mixture of the bis(bromomethyl) compounds 7a, b with p-tolylsulfonylmethyl isocyanide. 2-Hydroxy[3](1,8)biphenylenophane (5) and the [3](1,8)biphenylenophane hydrocarbon 6 were obtained by reduction of 4 with LiAlH4 and NaBH4, respectively. X-ray analyses of 4 and 6 illustrate the dramatic deformation of bond lengths and angles in these molecules.

2H NMR studies of phase behaviour and molecular motions of doped discotic liquid-crystalline systems

1990

Abstract A discotic triphenylene monomer as well as a dimer and a main chain polymer, all substituted with heptyloxy side groups, were doped with an electron acceptor (2,4,7-trinitrofluorenone (TNF)) to give charge transfer complexes. These doped systems were aligned in a magnetic field, thus proving their liquid crystallinity. 2H NMR measurements show that the electron acceptor molecules are incorporated into the columns built of triphenylene cores. In the charge transfer complex with the triphenylene monomer almost all the electron acceptor molecules stack in the columns even close to the clearing temperature T 1, while for the dimer and especially for the polymer a significant fraction o…

Synthesis of New Functionalized Discotic Liquid Crystals for Photoconducting Aplications

1996

Abstract The columnar structure of discotic liquid crystals has been shown to be well suited for electronic transport parallel to the columnar axis. To tailor the processibility and mesophase behavior of such materials, several hydroxytriphenylene derivatives were synthesized. These hydroxytriphenylenes can be converted into oligomers, networks or polymers. Further, they can be reduced to arenes which posses reactive sites for classical aromatic substitutions. A number of mixed tail triphenylene derivatives and fluorescent, low symmetry triphenylene discotic liquid crystals were synthesized and characterized.

A Precursor Route to Supramolecular Oligo(p-phenylene terephthalamide) Block Copolymers

2008

New soluble precursors for the step-wise synthesis of oligo(p-phenylene terephthalamide) block copolymers are described. Kevlar-like aramide oligomers up to the hexamer (six phenyl groups) were prepared in a polymer-analogous manner. Activating the carboxylic-acid-carrying oligomers as carbonyl chlorides while reversibly transforming the aromatic amides into imidoyl chlorides gave access to soluble precursors. The dimer and tetramer precursor were prepared and used in block copolymer synthesis. Single-crystal XRD confirmed the structure of the dimer precursor. Above a critical rod length, the Kevlar-like rod-coil block copolymers show strong aggregation in non-polar solvents such as chlorof…

Phase identification of triphenylene-based discotic monomer and its main chain polymers

1998

Abstract A monomer, 2,3,6,7,10,11-hexakispentyloxy triphenylene (HPT) possesses a triphenylene core as a discotic mesogen. Polymers containing this discotic mesogen have been studied using wide-angle X-ray and electron diffraction. HPT is known to show a discotic liquid crystal phase, noted as Dho (h for hexagonal bidimensional lattice, o for ordered molecular spacing in each column). In this paper, however, HPT liquid crystalline phases, heated up from the crystalline state and cooled down from the isotropic state, were characterized in the diameter dimensions. In addition. the diameters of the columns are close to a parameter of two separate crystals. A core orientation was, therefore, pr…

Rheological behavior and thermal stability of poly(phenylene sulfide)/vectra-B950 blends

1994

Blends of polyphenylene sulfide (PPS) with a commercial, wholly aromatic, liquid crystalline polymer (LCP), Vectra-B950, have been prepared by melt-blending. Their rheological behavior has been studied in order to determine if the LCP displays a processing aid ability, and under what conditions it gives rise to potentially reinforcing fibrils dispersed in the PPS matrix. The problem of the thermal stability of PPS/LCP blends, which has been considered by some authors as the main obstacle to the production of usable materials due to the evolution of gaseous substances during processing, has been discussed. © 1994 John Wiley & Sons, Inc.

The Nucleating Effect of a Semiflexible Liquid-Crystalline Polymer for the Crystallization of Poly(Phenylene Sulfide)

1995

Abstract Blends of poly(phenylene sulfide) and a semiflexible liquid-crystalline polymer have been prepared, in the whole range of concentration, by melt mixing. The effect of the LCP phase on the crystallization of PPS has been studied by non-isothermal and isothermal calorimetry. It has been found that the addition of only 2-5% LCP into PPS strongly increases the crystallization rate of the latter polymer. This effect has been interpreted as the result of an increased nucleation density. The morphology of the blends, studied by scanning electron microscopy, has shown that the two polymers are incompatible, although the phase dispersion is good. Under elongational flow, the dispersed phase…

Perimeter leakage current in polymer light emitting diodes

2009

Observation of leakage current paths through the device perimeter in standard poly(phenylene vinylene)-based light-emitting devices is reported. Perimeter leakage currents govern the diode performance in reverse and low positive bias and exhibit an ohmic character. Current density correlates with the perimeter-to-area ratio thus indicating that leakage currents are mainly confined on polymer regions in the vicinity of metallic contact limits (device perimeter). © 2008 Elsevier B.V. All rights reserved.

Synthesis of all-syn Functionalized Triphenylene Ketals

2011

The stereoselective synthesis of triphenylene ketals offers access to unique scaffolds. For a good performance in supramolecular applications an all-syn orientation of the functional groups is essential. The oxidative trimerization of catechol ketals by molybdenum pentachloride or mixtures with titanium tetrachloride leads to a template-directed formation. Several heterocyclic moieties are suitable for this transformation. A template-directed isomerization of anti,anti,syn isomers to the desired C 3 -symmetric derivative was demonstrated in two cases.