Search results for "polymer chemistry"
showing 10 items of 3410 documents
Iron(iii) oxamato-catalyzed epoxidation of alkenes by dioxygen and pivalaldehyde
1997
A new iron(III)–carbonato monomeric complex of orthophenylenebis( oxamato) (opba) 1 is synthesized, and spectroscopically and structurally characterized; it is a moderately efficient non-heme catalyst for the aerobic epoxidation of alkenes with co-oxidation of pivalaldehyde. Ruiz Garcia, Rafael, Rafael.Ruiz@uv.es ; Fernandez Picot, Isabel, Isabel.Fernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es
Tetraiodoethynyl resorcinarene cavitands as multivalent halogen bond donors
2014
The first examples of iodoethynyl resorcinarene cavitands as rigid 3D halogen bond (XB) donor molecules are presented. These concave macrocycles form strong, RXB = 0.78–0.83, halogen bonds with dioxane oxygen, pyridine nitrogen and a bromide anion in tetraproropyl ammonium bromide resulting in deep cavity cavitand structures.
Phosphororganische Verbindungen, 68. Darstellung und Eigenschaften von Tetrakis(diphenylphosphin)‐nickel(0)
1971
Die Titelsubstanz 1 wurde durch Einwirkung von Diphenylphosphin auf Bis-π-allyl-nickel, Tetrakis(triphenylphosphin)-nickel(0) (2), Nickelpulver oder Nickel(II)-bromid dargestellt. Ihre Struktur wurde durch Zerewitinoff-Bestimmung, IR- und NMR-Spektren abgesichert. Eine Alkylierung von metalliertem 1 gelang nicht. Organic Phosphorus Compounds, 68. Preparation and Properties of Tetrakis(diphenylphosphine)nickel(0) The title compound, 1, was prepared by reacting of diphenylphosphine with bis(π-allyl)nickel, tetrakis(triphenylphosphine)nickel(0) (2), nickel-powder, or nickel(II) bromide. The structure of 1 was elucidated by Zerewitinoff method, i. r. and n. m. r. spectra. The alkylation of meta…
Catalytic activity of solvated and unsolvated lanthanide halides in Friedel–Crafts acylations
2000
Abstract Anhydrous lanthanide halides — chlorides and bromides — can act as homogeneous catalysts of Friedel–Crafts acylations. The catalytic activity is related to the solubility of these anhydrous salts. More soluble THF or dioxane (Diox.) neodymium and samarium adducts are more active catalysts.
Studies of structural composition distribution heterogeneity in ethylene/1-hexene copolymers using thermal fractionation technique (SSA)
2005
Abstract Investigations into the compositional heterogeneity of ethylene/1-hexene copolymers obtained with various zirconocene/MAO catalysts, either homogeneous or supported on inorganic carriers such as a complex of magnesium chloride with tetrahydrofuran or methyl alcohol, were conducted. The dependence between metallocene structure, as well as catalyst immobilization, and the compositional heterogeneity of the related products was investigated. It was found that the heterogeneity of copolymers is determined by the metallocene catalyst structure. The amount of peaks on the DSC thermograms of copolymers and their division increase with the increase of bulkiness of the ligand in the catalyt…
Design of PNIPAAM covalently grafted on halloysite nanotubes as a support for metal-based catalysts
2016
A thermo-responsive polymer such as poly(N-isopropylacrylamide) (PNIPAAM) was covalently grafted on the external surface of halloysite nanotubes (HNTs) by means of microwave irradiation. This nanomaterial was used as a support and stabilizer for palladium nanoparticles. The obtained HNT–PNIPAAM/PdNPs was characterized by means of TGA, SEM, EDS and TEM analyses. The palladium content of the catalyst was estimated to be 0.4 wt%. The stability of the catalytic material at different temperatures (below and above the PNIPAAM lower critical solution temperature) was tested in the Suzuki reaction under microwave irradiation. In addition, TEM analysis after five consecutive runs was performed. The …
Measurements on the temperature dependence of the cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst
1979
The cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst and at low monomer concentrations shows, at −15°C, −45°C and −60°C, the same formal dependence on monomer concentration. The dependence on the catalyst concentration is approximately but not exactly of a third order.
Barrier properties of chitosan coated polyethylene
2012
The transfer properties of chitosan coated polyethylene (PE) films were studied. The barrier properties of non coated PE were not affected by relative humidity changes. The presence of the hydrophilic chitosan layer acted as a water reservoir on the polyethylene film surface which significantly promoted its sensitivity to the water vapour. The water vapour permeability increased 1.85 times at a higher RH. Coated PE films showed more than two-order decrease in the oxygen permeability (PO2) and three-order-decrease in the carbon dioxide permeability (PCO2). When the chitosan coated PE surface was exposed to the water vapour, the PO2 and the PCO2 were significantly increased. However, the perm…
Crystal structure of the molecular adduct of dimethyltin(IV) chloride with N,N′-ethylenebis(salicylideneiminato) nickel(II)
1974
Abstract N,N′-Ethylenebis(salicylideneiminato)nickel(II) behaves as a neutral bidentate ligand through its oxygen atoms forming binuclear complexes with organotin(IV) chlorides. The crystal structure of the dimethyl derivative is reported.
Die Cooligomerisierung von butadien mit α-hydroxycarbonsäureestern
1977
Abstract Glycolic acid butyl ester as well as lactic acid ethyl ester react with butadiene in the presence of palladium(II) acetylacetonate and triphenylphosphine as catalyst. The main product is the 2-trans, 7-octadienyl ether of the hydroxy acid ester, which is formed in yields from 65 to 80% at room temperature.