Search results for "polymerization"
showing 10 items of 1689 documents
Oxovanadium(IV) complexes with [ONNO]-chelating ligands as catalysts for ethylene homo- and copolymerization
2014
Oxovanadium(IV) complexes with (ONNO)-type tetradentate Schiff base ligands: salen, acacen, aceten, acetph (H2salen = N,N'-ethylenebis(salicylideneimine), H2aceten = N,N'-ethylenebis(2-hydroxyacetophenoneimine), H2acacen = N,N'-ethylenebis(acetylacetonimine), H 2 acetph = N ,N ' -phenylene-1,2-b is (2-hydroxyacetophenoneimine)), were the first time investi- gated in ethylene polymerization and ethylene/1-octene copo- lymerization processes. In general, all these complexes are moderately active precatalyst for ethylene polymerization up- on activation with EtAlCl2 and they give high molecular weight linear polyethylenes. Their activity in copolymeriza- tion was found relatively low. However,…
Synthesis and characterization of a novel dicyanamide-bridged Co(II) 1-D coordination polymer with a N 4 -donor Schiff base ligand
2017
The synthesis, structure and magnetic properties of a novel Co(II) 1D coordination polymer, [Co(L)(µ1,5-dca)(ClO4)2·MeOH]n (1) are described. Compound 1 contains two independent cationic Co(II) chains (CoA and CoB) which are parallel to the c direction and present short π-π and C-H⋯π interactions with two neighbouring chains along the b direction, giving rise to alternating layers of chains A and B in the bc plane. Variable-temperature magnetic susceptibility measurements shows a weak antiferromagnetic coupling among the adjacent cobalt(II) centres mediated through μ1,5-dca− bridge.
ATRP of Methacrylates Catalysed by Homo- and Heterobimetallic Ruthenium Complexes
2009
The catalytic activity of a series of ruthenium-based homo-and heterobimetallic complexes was determined by investigating the atom transfer radical polymerisation of methyl methacrylate. The complexes under investigation were [(arene)Ru(μ-Cl) 3 RuCl(C 2 H 4 )-(L)] (L = PCy 3 or a N-heterocyclic carbene ligand), [(p-cymene )-Ru(/l-Cl) 3 RuCl(=C=CHR)(PCy 3 )] (R = Ph or t-Bu), and [RuCl 2 -(p-cymene) {PCy 2 (CH2) 2 (n 5 -C 5 H 4 )TiX 2 (n 5 -C 5 H 5 )}] (X = Cl, F, and OBz). The catalytic activity of a variety of related [(p-cymene)-ClRu(μ-Cl) 2 Ru(O/\N)(=CHPh)] complexes (O^N is a Schiff base ligand) is also reported. The results clearly demonstrate that the ligands strongly affect the abili…
Ethylene homo- and copolymerization catalyzed by vanadium, zirconium, and titanium complexes having potentially tridentate Schiff base ligands
2021
Abstract New potentially tridentate Schiff base ligands, 2-[({4-[(3-N,N-dimethylamino)propyl] phenyl}imino)methyl]-4,6-di-tert-butylphenol (L1H) and 2-[{2-(N-phenyl-N-methylaminomethyl)-phenylimino}-methyl]-4,6-di-tert-butylophenol (L2H) were prepared and after deprotonation they were reacted with VOCl3 or MCl4 (where M = Zr or Ti) to produce corresponding complexes (L1-V, L2-V, L1-Zr, L2-Ti) with good yields. All new compounds were characterized by the 1H and 13C NMR as well as FTIR spectroscopic methods. Upon activation with Et2AlCl or EtAlCl2, both the vanadium complexes exhibited exceptionally high catalytic activities in the ethylene polymerization (up to 69,000 kg/(molV⋅h) for L1-V an…
Ring opening polymerization of ε-caprolactone initiated by titanium and vanadium complexes of ONO-type schiff base ligand
2021
AbstractA phenoxy-imine proligand with the additional OH donor group, 4,6-tBu2-2-(2-CH2(OH)-C6H4N = CH)C6H3OH (LH2), was synthesized and used to prepare group 4 and 5 complexes by reacting with Ti(OiPr)4 (LTi) and VO(OiPr)3 (LV). All new compounds were characterized by the FTIR, 1H and 13C NMR spectroscopy and LTi by the single-crystal X-ray diffraction analysis. The complexes were used as catalysts in the ring opening polymerization of ε-caprolactone. The influence of monomer/transition metal molar ratio, reaction time, polymerization temperature as well as complex type was investigated in detail. The complexes showed high (LTi) and moderate (LV) activity in ε-caprolactone polymerization a…
Dichlorovanadium (IV) complexes with salen-type ligands for ethylene polymerization
2008
Vanadium complexes with tetradentate salen-type ligands were first time explored in ethylene polymerizations. The effects of the vanadium complex structure, the alkyl aluminum cocatalysts type (EtAlCl2, Et2AlCl, Et3Al, and MAO), and the polymerization conditions (Al/V molar ratio, temperature) on polyethylene yield were explored. It was found that EtAlCl2 in conjunction with investigated vanadium complexes produced the most efficient catalytic systems. It was shown, moreover, that the structural changes of the tetradentate salen ligand (type of bridge which bond donor nitrogen atoms and type of substituent on aryl rings) affected activity of the catalytic system. The complexes containing li…
Ethylenebis(5-chlorosalicylideneiminato)vanadium dichloride immobilized on MgCl2 -based supports as a highly effective precursor for ethylene polymer…
2009
Ethylenebis(5-chlorosalicylideneiminato)vanadium dichloride supported on MgCl2(THF)2 or on the same carrier modified by EtnAlCl3−n, where n = 1–3, was used in ethylene polymerization in the presence of MAO or a common alkylaluminium compounds as a cocatalyst. The support type alter vanadium loading and also change the characteristic of the catalytic active sites. Et2AlCl is the best activator for a catalyst which has been immobilized on a nonmodified support, whereas the systems which contain a carrier which has been modified by an organoaluminium compound reveal the highest activity in conjunction with MAO. That difference, together with different temperature effects on polymerization effi…
Aggregation behavior of cationic nanohydrogel particles in human blood serum.
2014
For systemic siRNA delivery applications, well-defined drug carriers are required that guarantee stability for both carrier and cargo. Among various concepts progressing in market or final development, cationic nanohydrogel particles may serve as novel transport media especially designed for siRNA-in vivo experiments. In this work, the interaction of nanohydrogel particles with proteins and serum components was studied via dynamic light scattering in human blood serum as novel screening method prior to applications in vivo. The formation of larger aggregates mostly caused by charge interaction with albumin could be suppressed by nanogel loading with siRNA affording a neutral zeta potential …
The necessary chances of a thermodynamically metastable protein: inactivation and polymeritzation of human neuroserpin
2009
Serpins are a wide class of proteins with high structural similarity, characterized by a unique substrate-like inhibitory mechanism that resembles a "molecular mousetrap". The active serpin is characterized by a main 5-stranded β-sheet and an exposed Reactive Centre Loop, which acts as a bait for the target protease. The cleavage of the loop by the protease triggers the insertion of the loop into the β-sheet as a strand and the disruptive translocation of the protease. This peculiar conformational mobility is achievable since serpins fold into a metastable native conformation. This feature gives a selective advantage to the serpin family to develop inhibitory activities, but leaves these pr…
Sub-micron structured Polymethyl Methacrylate/Acrylonitrile-Butadiene rubber blends obtained via gamma radiation induced “in situ” polymerisation
2004
The morphology and properties of PMMA/rubber blends, obtained through gamma radiation induced “in situ” polymerization of methyl methacrylate (MMA) in the presence of small quantities of an acrylonitrile–butadiene based rubber (ABN), are presented. Different systems have been obtained by irradiating at a fixed irradiation dose rate and temperature, varying the integrated dose. All the blends obtained were characterized with respect to their melt state and solid state dynamic-mechanical response and mechanical tensile properties. In particular, the effect on the blend properties of prolonging the irradiation time was investigated. Furthermore, a morphological characterization through atomic …