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Complexation in polymerization

Independently of the interest of the CG complexes in polymerization catalysis, similar reactivity to that of metallocenes can be observed. For instance, the metathetical reaction of [(C5H4)SiMe2(Nt-Bu)]ZrCl2 with [Mg(C4H6)(thf)2] affords the Zr-butadiene complex (39)." ... [Pg.5297]

The general catalytic performance of these metal complexes in polymerization of olefins was screened by the following standard procedure The complexes (50 or 100 pmol) were activated with 100 mole equivalents of methylalumoxane (MAO) in toluene solution. The polymerization reaction was carried out at a temperature of 30°C, during which ethene was added with a flow of 40 L h"t After 4.5 h, the mixture was quenched with methanol, the solid polymer isolated, washed and dried. For benchmarking a nickel diimine complex [12a] with 2,6-(di-isopropyl) phenyl substituents at the imine nitrogen atoms (133) was also included. Tab. 3.2 shows the activity and polymer data. [Pg.83]

Collective structure factor 194-203, 214, 233, 251, 259, 272, 273, 280 Complexation in polymerization 148 Convective term 226 Crown ethers 9 Cyclohexane/methanol 213... [Pg.305]

Schultz R. G Chemistry of palladium complexes, in. Polymerization of norbornene systems catalyzed by palladium chloride. J. Polym. Sci., Part B Polym. Lett. 1966, 4, 541-546. [Pg.441]

Sophie M. Guillaume, Laurent Maron, and Peter W. Roesky, Catalytic Behavior of Rare-Earth Borohydride Complexes in Polymerization of Polar Monomers 1... [Pg.362]

Rutherford backscattering is ideal for investigations of diffusion near surfaces. An example is the RBS study of the diffusion of Cu(II) ions in polypropylene film oxidised between Cu foils [238]. Also the diffusion rates of copper carboxylate complexes in polymeric matrices have been studied [239] and that of iodoalkanes into polystyrene [240]. [Pg.446]

Mashima K, Nakayama Y and Nakamura A 1997 Recent trends in polymerization of a-olefins catalyzed by organometallic complexes of early transition metals Adv. Polym. Sc/. 133 1-54... [Pg.2538]

Beryllium Hydride. BeryUium hydride [13597-97-2] is an amorphous, colorless, highly toxic polymeric soHd (H = 18.3%) that is stable to water but hydroly2ed by acid (8). It is insoluble in organic solvents but reacts with tertiary amines at 160°C to form stable adducts, eg, (R3N-BeH2 )2 (9). It is prepared by continuous thermal decomposition of a di-/-butylberylhum-ethyl ether complex in a boiling hydrocarbon (10). [Pg.299]

Halophenols without 2,6-disubstitution do not polymerize under oxidative displacement conditions. Oxidative side reactions at the ortho position may consume the initiator or intermpt the propagation step of the chain process. To prepare poly(phenylene oxide)s from unsubstituted 4-halophenols, it is necessary to employ the more drastic conditions of the Ullmaim ether synthesis. A cuprous chloride—pyridine complex in 1,4-dimethoxybenzene at 200°C converts the sodium salt of 4-bromophenol to poly(phenylene oxide) (1) ... [Pg.330]

Other THF polymerization processes that have been disclosed in papers and patents, but which do not appear to be in commercial use in the 1990s, include catalysis by boron trifluoride complexes in combination with other cocatalysts (241—245), modified montmorrillonite clay (246—248) or modified metal oxide composites (249), rare-earth catalysts (250), triflate salts (164), and sulfuric acid or Aiming sulfuric acid with cocatalysts (237,251—255). [Pg.365]

The neat resin preparation for PPS is quite compHcated, despite the fact that the overall polymerization reaction appears to be simple. Several commercial PPS polymerization processes that feature some steps in common have been described (1,2). At least three different mechanisms have been pubUshed in an attempt to describe the basic reaction of a sodium sulfide equivalent and -dichlorobenzene these are S Ar (13,16,19), radical cation (20,21), and Buimett s (22) Sj l radical anion (23—25) mechanisms. The benzyne mechanism was ruled out (16) based on the observation that the para-substitution pattern of the monomer, -dichlorobenzene, is retained in the repeating unit of the polymer. Demonstration that the step-growth polymerization of sodium sulfide and /)-dichlorohenzene proceeds via the S Ar mechanism is fairly recent (1991) (26). Eurther complexity in the polymerization is the incorporation of comonomers that alter the polymer stmcture, thereby modifying the properties of the polymer. Additionally, post-polymerization treatments can be utilized, which modify the properties of the polymer. Preparation of the neat resin is an area of significant latitude and extreme importance for the end user. [Pg.442]

Economic considerations in the 1990s favor recovering butadiene from by-products in the manufacture of ethylene. Butadiene is a by-product in the C4 streams from the cracking process. Depending on the feedstocks used in the production of ethylene, the yield of butadiene varies. Eor use in polymerization, the butadiene must be purified to 994-%. Cmde butadiene is separated from C and C components by distillation. Separation of butadiene from other C constituents is accomplished by salt complexing/solvent extraction. Among the solvents used commercially are acetonitrile, dimethyl acetamide, dimethylform amide, and /V-methylpyrrolidinone (13). Based on the available cmde C streams, the worldwide forecasted production is as follows 1995, 6,712,000 1996, 6,939,000 1997, 7,166,000 and 1998, 7,483,000 metric tons (14). As of January 1996, the 1995 actual total was 6,637,000 t. [Pg.494]

Studies of the copolymerization of VDC with methyl acrylate (MA) over a composition range of 0—16 wt % showed that near the intermediate composition (8 wt %), the polymerization rates nearly followed normal solution polymerization kinetics (49). However, at the two extremes (0 and 16 wt % MA), copolymerization showed significant auto acceleration. The observations are important because they show the significant complexities in these copolymerizations. The auto acceleration for the homopolymerization, ie, 0 wt % MA, is probably the result of a surface polymerization phenomenon. On the other hand, the auto acceleration for the 16 wt % MA copolymerization could be the result of Trommsdorff and Norrish-Smith effects. [Pg.430]

Cyclopentadiene itself has been used as a feedstock for carbon fiber manufacture (76). Cyclopentadiene is also a component of supported metallocene—alumoxane polymerization catalysts in the preparation of syndiotactic polyolefins (77), as a nickel or iron complex in the production of methanol and ethanol from synthesis gas (78), and as Group VIII metal complexes for the production of acetaldehyde from methanol and synthesis gas (79). [Pg.435]

A living cationic polymeriza tion of isobutylene and copolymeriza tion of isobutylene and isoprene has been demonstrated (22,23). Living copolymerizations, which proceed in the absence of chain transfer and termination reactions, yield the random copolymer with narrow mol wt distribution and well-defined stmcture, and possibly at a higher polymerization temperature than the current commercial process. The isobutylene—isoprene copolymers are prepared by using cumyl acetate BCl complex in CH Cl or CH2CI2 at —30 C. The copolymer contains 1 8 mol % trans 1,4-isoprene... [Pg.480]

The conjugated stmcture of 1,3-butadiene gives it the abiUty to accept nucleophiles at both ends and distribute charge at both carbon 2 and 4. The initial addition of nucleophiles leads to transition states of TT-ahyl complexes in both anionic and transition-metal polymerizations. [Pg.530]


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See also in sourсe #XX -- [ Pg.148 ]




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Complexes polymeric

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