Search results for "GOME"

POSS nanostructures in catalysis

2020

Polyhedral oligomeric silsesquioxanes (POSS) are organic-inorganic hybrid molecules piquing the interest of researchers thanks to their synergistic features. The great versatility of POSS nanostructures arises from the easy tunability of peripheral organic moieties combined with the high thermal and chemical stability of the inner inorganic core. In this review, we highlight the use of POSS nanostructures as molecular precursors for the synthesis of homogeneous and heterogeneous catalysts able to promote many processes including alkene epoxidation, C-C bond formation, CO2 conversion, "click reactions", hydrogenation, and ethylene polymerisation, among others. In this scenario, POSS units fo…

Keyhole Limpet Hemocyanin (KLH): Slow In Vitro Reassociation of KLH1 and KLH2 from Immucothel®

1998

Abstract Following our in vitro reassociation of keyhole limpet hemocyanin subunits in the presence of high concentrations (100 mM each) of calcium and magnesium chloride (Harris et al., 1997a, Micron 28, 31–41; 1997b, Micron 28, 43–56), we have now extended our investigations by using a buffer system containing a lower concentration of the two divalent cations (10 mM each). Reassociation of mixed KLH subunits present in the commercially available product Immucothel® was performed using a standardized buffer solution containing 50 mM Tris–HCl, 150 mM NaCl, 10 mM CaCl2 and 10 mM MgCl2 (pH 7.4) over a minimum period of one week, at 4°C. This solution was selected as being close to our KLH sta…

2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides: Synthesis, characterization and ethylene oligomerization

2017

Abstract 2-Chloro/phenyl-7-arylimino-6,6-dimethylcyclopenta[b]pyridylnickel chlorides (Ni1–Ni8) were synthesized from the respective ligands L1–L8 and characterized. Upon activation with either methylaluminoxane (MAO) or ethylaluminium sesquichloride (EASC), they show high catalytic activity of up to 10.84 × 106 g(oligomer) mol− 1(Ni) h− 1 in ethylene oligomerization. The products range from butenes to dodecenes for Ni1–Ni4, but are limited to butenes and hexenes in the case of Ni5–Ni8. DFT calculations indicate that the Ni C bond length in the model alkyl complexes depends both on the nature of the substituents at the heterocycles and the kind of the alkyl group, shedding some light on the…

Pentadecamer 2,5-Dipropoxy-1,4-phenylenevinylene

2002

The conjugated, all-(E)-configured pentadecamer 2,5-dipropoxy-1,4-phenylenevinylene 1j was prepared by a multistep synthesis on the basis of hydroquinone. The procedure consists of a general method for the repetitive extension of oligo(phenylenvinylene) chains by two styryl units (7a ⇄ 10 ⇄ 12 ⇄ 14). The relatively rigid oligomer 1j represents a molecular wire of about 100 A. The absorption of 1j provides a proof for the convergence theory for electronic properties of conjugated oligomers with increasing number of repeat units. The corresponding conjugated polymer 1p with the same substitution matches the values which were extrapolated from the oligomer series 1a−1j. (© Wiley-VCH Verlag Gmb…

Relationship between structure and electroluminescence of oligo(p-phenylenevinylene)s

1998

The preparation of LEDs with poly(p-phenylenevinylene) (PPV) as emitting material is well established, However, due to the presence of a distribution of conjugated chain lengths in the polymer, systematic investigations of the electroluminescence with polymeric materials are difficult, as far as the optical emission is concerned. We are studying the relationship between structural variation of substituted oligo(p-phenylenevinylene)s and their electroluminescent behaviour using a series of distyrylbenzenes with a variety of substituents in order to investigate their influence on the electroluminescence (EL). Furthermore, we synthesized a homologous series of monodisperse oligo(2,5-dipropoxy-…

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…

The effect of macromolecular architecture of ethylene copolymers with multi-alkenylsilsesquioxane on morphological, rheological and dynamic mechanica…

2021

Abstract The influence of the degree and the way of incorporation of multi-alkenylsilsesquioxane into the polymer chain on morphological, rheological and dynamic mechanical parameters were determined. It was found that POSS incorporated into the polymer chain was located outside the crystalline structure of lamella in amorphous phase. The incorporation of POSS-6-2 as a pendant group resulted in significant increase of separation of macromolecules. The key factor in rheological and dynamic mechanical behavior of copolymers turned out to be the way of POSS incorporation into the polymer chain. The incorporation of POSS into the polymer chain as a pendant group resulted in decreased relaxation…

Calculation of low bandgap homopolymers: Comparison of TD-DFT methods with experimental oligomer series

2016

Made available in DSpace on 2018-12-11T17:26:45Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-02-01 The performance of different DFT functionals (B3LYP, BHLYP, CAM-B3LYP, M06HF) on the prediction of vertical transition energies Evert of low bandgap homopolymers is tested against the experimentally available oligomer series (thienopyrazines and thienothiophenes). This allows for a detailed and accurate comparison on the consistency of DFT methods for chainlength evolution and polymer limit prediction, and for an understanding of geometry and time-dependent contributions to Evert by combinatorial analysis. Together with former studies on wide/medium bandgap polymers and low bandgap c…

1986

Preparation d'oligosiloxanes et de polyarylates avec des groupes mesogenes fixes lateralement

Automated Large-Scale Synthesis of Supramolecular Oligo(p-benzamide) Block Copolymers

2007

A fully automated large-scale synthesis procedure has been developed that allows the preparation of supramolecular rod−coil copolymers on a 100 g scale. The new reaction cycle allows the stepwise growth of oligo(p-benzamide)s onto the chain end of amine-terminated polymers. Amine-terminated poly(ethylene glycol) (PEG, Mn = 5000 g mol-1) and poly(styrene) (PS, Mn = 2950 g mol-1) were prepared, and an octa(p-benzamide) oligomer block was grown from the chain end in an automated computer-controlled reaction cycle. Plotting the apparent molecular weight of the PEG copolymer against the number of reaction cycles revealed a linear relationship, which emphasized the high level of control this meth…