Search results for "Ziegler-Natta polymerization"
showing 8 items of 8 documents
Polypropylene and poly(ethylene-co-1-octene) effective synthesis with diamine-bis(phenolate) complexes: Effect of complex structure on catalyst activ…
2017
A series of group 4 metal complexes bearing amine-bis(phenolate) ligands with the amino side-arm donor: (μ-O)[Me2N(CH2)2N(CH2-2-O-3,5-tBu2-C6H2)2ZrCl]2 (1a), R2N(CH2)2N(CH2-2-O-3-R1-5-R2-C6H2)2TiCl2 (R = Me, R1, R2 = tBu (2a), R = iPr, R1, R2 = tBu (2b), R = iPr, R1 = tBu, R2 = OMe (2c)), and Me2N(CH2)2N(CH2-2-O-3,5-tBu2-C6H2)(CH2-2-O-C6H4)TiCl2 (2d) are used in ethylene and propylene homopolymerization, and ethylene/1-octene copolymerization. All complexes, upon their activation with Al(iBu)3/Ph3CB(C6F5)4, exhibit reasonable catalytic activity for ethylene homo- and copolymerization giving linear polyethylene with high to ultra-high molecular weight (600·× 103–3600·× 103 g/mol). The activi…
Dichlorovanadium(IV) diamine-bis(phenolate) complexes for ethylene (co)polymerization and 1-olefin isospecific polymerization
2018
Abstract Two vanadium complexes bearing amine-bis(phenolate) ligands with the amino side-arm donor, [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)2}Cl2] (1) and [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)(CH2-2-O-C6H4)}Cl2] (2), were synthesised and characterized by FTIR and 1H NMR spectroscopy. Upon activation with Al(iBu)3/Ph3CB(C6F5)4, these complexes became active catalysts for 1-octene polymerization giving highly stereoregular polymers (mmmm ∼ 90%) having regioirregularly arranged units. The catalytic activity of the catalysts in ethylene homo- and copolymerization, and their ability to incorporate a comonomer were highly dependent on both the activator type and the complex structure. 1/EtAlCl2 exhi…
Synthesis and catalytic performance in ethylene and 1-octene polymerization of chlorotitanium(IV) silsesquioxane complexes. Effect of increasing liga…
2016
Abstract The series of titanasilsesquioxanes that differ in a way of binding to the transition metal ( via one, two or three oxygen atoms) and type of nonreactive substituents bonded to inorganic oxygen-silicon cage ( i -Bu, Ph, c -C 6 H 11 ) were prepared by reacting of TiCl 4 with 1 eqv. of the silsesquioxane ligand. Upon treatment with an appropriate cocatalyst, all titanium precatalysts are active in ethylene and 1-octene polymerization and produce from low to high molecular weight polyethylenes and moderately ([ mmmm ] = 44–74%) isotactic poly(1-octene)s. The influence of polymerization parameters, type of cocatalyst and the silsesquioxane structure on the catalytic behavior of the tit…
Olefin polymerization and copolymerization by complexes bearing [ONNO]-Type salan ligands: Effect of ligand structure and metal type (titanium, zirco…
2014
A series of novel titanium(IV) complexes bearing tetradentate [ONNO] salan type ligands: [Ti{2,2′-(OC6H3-5-t-Bu)2-NHRNH}Cl2] (Lig1TiCl2: R = C2H4; Lig2TiCl2: R = C4H8; Lig3TiCl2: R = C6H12) and [Ti{2,2′-(OC6H2-3,5-di-t-Bu)2-NHC6H12NH}Cl2] (Lig4TiCl2) were synthesized and used in the (co)polymerization of olefins. Vanadium and zirconium complexes: [M{2,2′-(OC6H3-3,5-di-t-Bu)2-NHC6H12NH}Cl2] (Lig4VCl2: M = V; Lig4ZrCl2: M = Zr) were also synthesized for comparative investigations. All the complexes turned out active in 1-octene polymerization after activation by MAO and/or Al(i-Bu)3/[Ph3C][B(C6F5)4]. The catalytic performance of titanium complexes was strictly dependent on their structures an…
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…
A comparative study on the polymerization of 1-octene promoted by vanadium and titanium complexes supported by phenoxyimine and salen type ligands
2013
Polymerizations of 1-octene were carried out in the presence of vanadium and titanium complexes bearing salen-type or phenoxyimine ligands activated with various co-catalysts. Vanadium complexes turned out active only in conjunction with MAO, whereas the titanium ones were active in combination with Al(i-Bu)3/Ph3CB(C6F5)4. The activity of all catalysts was moderate or low and it was dependent on the ligand type: bis(phenoxyimine) complexes were more active than the salen ones. Both vanadium and titanium catalytic systems produced poly(1-octene)s possessing atactic structures with [mmmm] sequences in the range from 12 to 56 % at room temperature. A temperature decrease to 0.5 °C for the reac…
Novel diamine-bis(phenolate) Ti(IV) complexes – tuning the complex structure to control catalytic properties in α-olefin polymerization
2016
Abstract Four monomeric titanium(IV) dichloride complexes of amine-bis(phenolate) ligands having an extra donor arm (2a–2d) and one oxo-bridged complex 3 were successfully synthesized in the reaction of TiCl4 with a sodium salt of the appropriate ligand, and they were characterized by 1H NMR spectroscopy. The ligands had either a dimethylamino side‐arm donor and t-Bu substituents on both (1a) and one (1d) phenolate rings or a diisopropylamino side-arm donor and t-Bu (1b) and t-Bu along with OMe (1c) phenolate substituents. All complexes upon activation with [Ph3CB(C6F5)4] and MAO were used to catalyze polymerization of 1-octene (in liquid monomer) into poly(1-octene). Their activities as we…
Synteza bimetalicznego silseskwioksanowego kompleksu tytanu(IV) i jego polimerycznego odpowiednika oraz ich właściwości katalityczne w polimeryzacji …
2016
Zsyntetyzowano, a następnie scharakteryzowano dwa tytanosilseskwioksany: nowy, nieznany dotąd z literatury, tetrachloroditytanosilseskwioksan (2) i jego polimeryczny odpowiednik (3). Zbadano właściwości katalityczne otrzymanych związków w polimeryzacji etylenu i 1-oktenu. Obydwa prekatalizatory, po aktywacji za pomocą Et2AlCl lub EtAlCl2, katalizują polimeryzację etylenu do polietylenu (PE) o małej masie molowej, która zmniejsza się zarówno ze wzrostem temperatury reakcji, jak i stosunku molowego Al:Ti. Kompleks (2) w połączeniu z metyloaluminoksanem lub związkami boru jest także aktywny w polimeryzacji 1-oktenu.