Search results for "polymerization"
showing 10 items of 1689 documents
Styrene polymerization using nickel(II) complexes as catalysts
2005
International audience; Styrene polymerization is investigated with neutral and cationic Ni(II) complexes, i.e. Ni(bipy)Me-2, 1, Ni(bipy)Br-2, 2, Ni(phen)Br-2, 3, or Ni(Me(2)phen)Br-2, 4, Ni(acac)(2), 5, (bipy = 2,2 '-bipyridine, phen = phenanthroline, Me,phen = 2,9-dimethyl-1, 10-phenanthroline, acac acetylacetonate), activated by [NHMe2Ph][B(C6F5)(4)] or B(C6F5)(3) as cocatalysts, in the presence of AlMe3. The influence on the polystyrene features and the reaction kinetics of the nickel complex and boron activator, the Al/Ni or B/Ni molar ratios as well as the monomer concentration are studied. Catalytic systems derived from 2, 3 or 5 and [NHMe2Ph][B(C6F5)(4)] at a Ni:B:Al ratio of 1: 1:5…
Polietylen liniowy małej gęstości
2002
Artykuł o charakterze przeglądowym dotyczy jednego z gatunków polietylenu, tj. liniowego polietylenu małej gęstości (PE-LLD) stanowiącego kopolimer etylenu z niewielką ilością (kilku %) wyższej l-olefiny otrzymywany metodą polimeryzacji koordynacyjnej z udziałem metaloorganicznych układów katalitycznych. Omówiono wpływ typu katalizatora, w szczególności nowoczesnych układów metalocenowych, na aktywność w kopolimeryzacji i efektywność wbudowania komonomeru do łańcucha polietylenowego. Przedstawiono przemysłowe metody otrzymywania PE-LLD oraz charakterystykę tego produktu na tle znanych gatunków polietylenu - PE-LD i PE-HD. Omówiono także wpływ budowy chemicznej PE-LLD na jego podstawowe właś…
Effect of buffer nature and concentration on the chromatographic performance of basic compounds in the absence and presence of 1-hexyl-3-methylimidaz…
2019
Abstract In reversed-phase liquid chromatography, the performance for basic compounds is affected by the interaction of the protonated (cationic) species with the anionic free silanols on the alkyl-bonded stationary phases. Using aqueous-organic mobile phases in the absence of additives, the retention may be too high, and the peaks be broad and asymmetric. The performance is improved by addition to the mobile phase of ionic liquids, from which 1-hexyl-3-methylimidazolium chloride ([C6MIm][Cl]) has especially good characteristics. A recent report has also revealed that the use of the phosphate system as buffer, at varying concentration and pH, may have a significant role in the chromatograph…
Effect of hydrogen on the ethylene polymerization process over Ziegler–Natta catalysts supported on MgCl2(THF)2. I. Studies of the chain‐transfer rea…
2001
The effect of hydrogen on the molecular weight of polyethylene obtained over vanadium catalysts (based on VCl4 and VOCl3) supported on MgCl2(THF)2 was studied and the results were compared to those obtained for similar titanium catalysts. It was confirmed that the dependencies of the transfer reaction on the hydrogen concentration are a half‐order in all investigated systems. However, the transition metal of the catalytic site affects the ratio of the transfer rate with hydrogen to the propagation rate (ktr,H/kp) and the results showed that hydrogen is a more effective agent of polyethylene molecular weight control in vanadium‐based systems as compared to the titanium catalyst.
Quadruply-bonded dimolybdenum compounds: Reactivity towards TCNE. Structural evidences for the 1-D polymer [Mo2(O2 CCF3)4(TCNE)]∞
2005
cited By 3; International audience; Reaction of [Mo2(O2CR)4] (R = CF 3, 1) with TCNE in toluene affords the new compound [Mo2(O2CCF3)4 (TCNE)·6H5CH3 (2). The structure of 2 is built on [Mo2(O2 CCF3)4] fragments having the usual paddlewheel structure of 1 (Mo-Mo 2.1117(8) Å) and TCNE units. Each polynitrile moiety acts as a bridging ligand between two Mo2 fragments (Mo-N 2.875(4) Å) affording 1-D polymeric chains crossing in the crystal; the toluene molecules occupy the cavities between the chains. 13C NMR, IR and electrochemical data clearly show that formation of 2 does not involve electron density transfer from dimolybdenum fragment to the TCNE unit, which remains in 2 in its neutral stat…
Electro-conversion as sustainable method for the fine chemical production from the biopolymer lignin
2018
Lignin, one of the most abundant polymers in nature, qualifies itself by the polyphenolic structure as potential renewable feedstock for the production of bio-based aromatic fine chemicals. However, the natural complexity and degradation stability of lignin make the depolymerization a highly challenging task. Several efforts have been pursued for the selective degradation of the biopolymer into suitable compounds. However, there are only a few technical approaches for the degradation of lignin to aromatic fine chemicals. Organic electrosynthesis is the synthetic method that enables the direct use of electricity for the production of valuable compounds. Moreover, electro-organic synthesis re…
Intermolecular interactions in dictating the self-assembly of halogen derivatives of bis-(N-substituted oxamato)palladate(ii) complexes
2016
Three palladium(II) complexes of formula (n-Bu4N)2[Pd(4-Fpma)2] (1), (n-Bu4N)2[Pd(4-Clpma)2]·4H2O (2) and (n-Bu4N)2[Pd(4-Brpma)2]·4H2O (3) [n-Bu4N+ = tetra-n-butylammonium cation, 4-Fpma = N-4-fluorophenyloxamate, 4-Clpma = N-4-chlorophenyloxamate and 4-Brpma = N-4-bromophenyloxamate] have been prepared and their structures determined by single crystal X-ray diffraction. Each palladium(II) ion in 1–3 is four-coordinate with two oxygen and two nitrogen atoms from two fully deprotonated oxamate ligands building PdO2N2 square planar surroundings, the oxamate ligands exhibiting trans (1 and 2) and cis (3) dispositions. The fluoro substituent and the organic counterion in 1 are involved in C–H⋯F…
On Demand One-Pot Mild Preparation of Layered Double Hydroxides and Their Hybrid Forms: Advances through the Epoxide Route.
2019
Epoxide ring opening driven alkalinization process was explored with the aim of preparing layered double hydroxide (LDH) phases on demand, at room temperature. Employing iodide as nucleophilic agent, the precipitation reaction can be driven under much lower halide concentrations. This scenario favors the selective intercalation of concomitant bulky oxo anions as nitrate or perchlorate in the LDH products, allowing for the one-pot synthesis of an LDH able to delaminate in formamide. Even large dicarboxylic acids, - O2 C-(CH2 )n -CO2 - , with n up to 8, can be quantitively intercalated within the growing LDH phase, providing a versatile one-pot route for hybrid LDHs as well. Under the mild co…
Silintaphin-1 - interaction with silicatein during structure-guiding bio-silica formation
2011
Silicateins are unique enzymes of sponges (phylum Porifera) that template and catalyze the polymerization of nanoscale silicate to siliceous skeletal elements. These multifunctional spicules are often elaborately shaped, with complex symmetries. They carry an axial proteinaceous filament, consisting of silicatein and the scaffold protein silintaphin-1, which guides silica deposition and subsequent spicular morphogenesis. In vivo, the synthesis of the axial filament very likely proceeds in three steps: (a) assembly of silicatein monomers to form one pentamer; (b) assembly of pentamers to form fractal-like structures; and finally (c) assembly of fractal-like structures to form filaments. The …