n-Propylsulfonic acid-functionalized porous and nonporous silica materials are evaluated in the ring-opening polymerization of -caprolactone. All catalysts allow for the controlled polymerization of the monomer, producing polymers with controlled molecular weights and narrow polydispersities. Polymerization rates are low, with site-time yields generally 1-3 orders of magnitude lower than metalb...

The previously unknown methallylnickel 2-diorganophosphanylphenolates (R=Ph, cHex) were synthesized and found to catalyze the polymerization of ethylene. To explore the potential for ligand-tuning, a variety of P-alkyl- and P-phenyl-2-phosphanylphenols was synthesized and allowed to react with [Ni(cod)(2)] (cod=1,5-cyclooctadiene) or with NiBr(2).DME and NaH. The complexes formed in situ with [...

Poly(ethylene glycol) (PEG)-armed Ru(II)-bearing microgel-core star polymer catalysts were used for the transfer hydrogenation of ketones. The star catalysts (Ru(II)-PEG Star) were one-pot synthesized by ruthenium-catalyzed living radical polymerization of poly(ethylene glycol) methyl ether methacrylate (PEGMA) and a sequential linking reaction with ethylene glycol dimethacrylate (1) and diphen...

the stereospecific polymerization of conjugated dienes began in 1954 with the first catalysts obtained by combining ticl4 or ticl3 with aluminum-alkyls, i.e. the catalytic systems previously employed for ethylene and propylene polymerizations. subsequently, many other catalytic systems were obtained and examined by a combination of transition metal or lanthanide compounds with appropriate alkyl...

supported catalysts synthesized via the interaction of mg(oet)2 with ticl4 in the presence or absence of an internal stereoregulating donor (di-n-butyl phthalate), with different solvents (chlorobenzene, n-undecane, n-heptane) at different titanation temperatures have been studied by a set of physicochemical methods. data on the chemical composition, x-ray structure and pore structure of these ...

We report a catalytic system that produces olefin block copolymers with alternating semicrystalline and amorphous segments, achieved by varying the ratio of alpha-olefin to ethylene in the two types of blocks. The system uses a chain shuttling agent to transfer growing chains between two distinct catalysts with different monomer selectivities in a single polymerization reactor. The block copoly...

A heterobimetallic catalyst, {Ti--Cr}, consisting of a constrained-geometry titanium olefin polymerization center (CGC(Et)Ti) covalently linked to a chromium bis(thioether)amine ethylene trimerization center (SNSCr) was synthesized and fully characterized. In ethylene homopolymerizations it affords linear low-density polyethylene with molecular weights as high as 460 kg·mol(-1) and exclusively ...

Dinickel bisphenoxyiminato complexes based on highly substituted p- and m-terphenyl backbones were synthesized, and the corresponding atropisomers were isolated. In the presence of a phosphine scavenger, Ni(COD)2, the phosphine-ligated syn-dinickel complexes copolymerized α-olefins and ethylene in the presence of amines to afford 0.2-1.3% α-olefin incorporation and copolymerized amino olefins a...

Homogeneous molecular catalysts are immobilzed in a well-defined fashion on individual silica nanoparticles with a narrow particle size distribution by covalent attachment. This synthetic methodology is demonstrated with modified salicylaldiminato-substituted titanium(IV) complexes incorporating a trimethoxysilaneterminated linker: dichloro-bis[κ2-N,O-6-(3-(trimethoxysilyl)propoxyphenylimino)-2...