Search results for "Oxide"
showing 10 items of 6424 documents
The influence of hydrophobic substitution on self-association of poly(ethylene oxide)-b-poly(n-alkyl glycidyl carbamate)s-b-poly(ethylene oxide) trib…
2007
Abstract A series of amphiphilic poly(ethylene oxide)-b-poly(n-alkyl glycidyl carbamate)s-b-poly(ethylene oxide) triblock copolymers were synthesized by reaction between poly(ethylene oxide)-b-polyglycidol-b-poly(ethylene oxide) precursor copolymer and four n-alkyl isocyanates: ethyl, propyl, butyl and pentyl. After dissolution in water at room temperature the copolymers spontaneously form micelles. The critical micellization concentrations were determined by UV–VIS spectroscopy. The dimensions of the micelles, the aggregation numbers, and in some cases the micellar shape were determined by dynamic and static light scattering in a relatively broad temperature range. Special attention has be…
2-(Mesitylmethylsulfanyl)pyridineN-oxide–18-crown-6 (2/1)
2008
In the title compound, 2C(15)H(17)NOS·C(12)H(24)O(6), the asymmetric unit consists of one N-oxide derivative and one-half of the 18-crown-6 ether, which lies on an inversion centre. In the crown ether, the O-C-C-O torsion angles indicate a gauche conformation of the ethyl-eneoxy units, while the C-O-C-C torsion angles indicate planarity of these segments. In the N-oxide unit, the dihedral angle between the pyridine and benzene rings is 85.88 (12)°. The crystal packing is stabilized by weak C-H⋯O hydrogen bonds and C-H⋯π inter-actions.
Conformational stability of oligoferrocene oligoamide foldamers
2016
Abstract Organometallic oligoamides built from three to four ferrocene amino acid units ( H-Fca-OH , 1-amino-1′-ferrocene carboxylic acid) fold into hydrogen bonded secondary structures featuring eight-membered rings by cooperative hydrogen bonds. NMR studies and DFT calculations (CAM-B3LYP, LANL2DZ, IEFPCM (THF)) reveal that the organometallic zigzag foldamer structures are highly resistant toward denaturation by hydrogen bond acceptors such as dimethyl sulfoxide and 2,4-lutidine. Replacing one ferrocene amino acid unit by the organic α -amino acid glycine at the C -terminal end (Fca → Gly) significantly destabilizes the secondary zigzag structure facilitating denaturation by DMSO. Highly …
Progress in polymeric material for hydrogen storage application in middle conditions
2014
Hydrogen sorption using a manganese oxide anchored to PEEK (Poly(ether-ether-keton)) matrix was studied. The functionalization process and the obtained results on hydrogen storage capability of the synthesized polymer are reported. The functionalised polymer was characterised by Scanning Electron Microscopy, Transmission Electron Microscopy, X-ray diffraction and Volumetric Hydrogen sorption measurements. Different synthesis conditions in terms of precursor concentration and reaction time were used and the direct correlation between manganese oxide percentage and hydrogen storage capability was confirmed. In this way different powders were synthesised. It is assumed that the sample with 78 …
Electrocatalytic Properties of Carbosilane‐Based Hyperbranched Polymers Functionalized with Interacting Ferrocenyl Units
2012
Two types of hyperbranched ferrocene-containing polycarbosilanes were obtained by hydrosilylation of polydiallylmethylsilane (hb-PDAMS) and polymethyldiundecenylsilane (hb-PMDUS) with diferrocenylmethylsilane. The redox properties of both polymers have been investigated both in solution and confined onto platinum electrodes. The electrocatalytic activity of polymer-modified electrodes toward the reduction of oxygen as well as the electrochemical reduction and oxidation of hydrogen peroxide has been examined.
A general concept for the introduction of hydroxamic acids into polymers.
2019
Polyethers (PEG) with hydroxamic acid groups enable chelation of a variety of metal ions, coating of metal oxide surfaces and stabilization of nanoparticles. In contrast to catechol, hydroxamic acids are oxidation stable and biocompatible.
Electrochemical study on a tricyclic 1,1,1-tricar-bonyl-2,3-1 diazaferrole derivative. II. Activation of carbon monoxide replacement by electron tran…
1986
Etudes, par voltammetrie cyclique, de la reduction electrochimique du complexe de diazaferratricyclodecene, en presence de P(OMe) 3
Photocatalytic degradation of 4-nitrophenol in aqueous suspension by using polycrystalline TiO2 impregnated with functionalised Cu(II)-porphyrin or C…
2003
The photocatalytic activity of polycrystalline TiO2 samples impregnated with functionalized Cu(II)- or metal-free porphyrins has been investigated. A probe reaction, i.e., 4-nitrophenol (4-NP) photodegradation in aqueous suspension, has been used. The results indicated that the presence of the sensitizers is beneficial for the photoactivity and suggest an important role of Cu(II). A comparison with similar samples impregnated with modified Cu(II)- and metal-free phthalocyanines showed that the presence of porphyrin is more beneficial both for the decomposition rate of 4-nitrophenol and for the disappearance of nonpurgeable organic carbon (NPOC). Experiments were carried out by using cutoff …
Structural evolution of Pt/ceria-zirconia TWC catalysts during the oxidation of carbon monoxide
2004
The structural evolution of two Pt/ceria–zirconia catalysts, characterized by different amounts of supported Pt, was monitored by in situ X-ray diffraction during the anaerobic oxidation of CO at different temperatures. In a first phase, oxygen coming from the surface layers of the ceria–zirconia mixed oxide is consumed and no structural variation of the support is observed. After this induction time, bulk reduction of Pt/ceria–zirconia takes place as a step-like process, while the CO2 production continues at a nearly constant rate. This behavior is totally different from that of the metal-free support in similar reaction conditions, that show a gradual bulk reduction. In repeated oxidation…
Progress in Understanding of the Interactions between Functionalized Polyolefins and Organo-Layered Double Hydroxides
2013
The dispersion of organo-layered double hydroxides (O-LDH) in functionalized polyolefins (POs) is investigated. Two different polyethylene matrices (maleic anhydride (MAH) and diethyl maleate functionalized) are tested and a hydrogenated fatty acid modified LDH is used. The attention is focused on evidencing the interaction between the functional groups of the polymer and the O-LDH through FT-IR. Moreover, a combination of solvent fractionation, morphological, and rheological characterizations enables to gain a deeper insight into the structure of these composites. In particular, the formation of bridging bonds between the particles and MAH functionalized macromolecules is assumed, possibly…