beside ziegler-natta and phillips catalysts the development of methylaluminoxane (mao) as cocatalyst incombination with metallocenes or other transition metal complexes for the polymerization of olefins haswidely increased the possibilities in controlling the polymer composition, polymer structure, tacticity and special properties with high precision. these catalysts allow the synthesis of isot...

a two-dimensional (2d) single particle model for the copolymerization of propylene-ethylene with heterogeneous ziegler-natta catalyst is developed. the model accounts for the effects of the initial shape of the catalyst and carck/ pore patterns on the copolymer composition, polymerization rate and the average molecular weight properties. the spherical and oblate ellipsoidal shapes of catalyst p...

A new class of complexes based on titanium(IV) bearing a bisanionic mer-tridentate N-heterocyclic carbene ligand were investigated for the copolymerization of cyclohexene oxide with CO2. Upon addition of [PPN]X' salts, all complexes were found to be active and highly selective toward the formation of poly(cyclohexene oxide-alt-carbon dioxide).

Polyoxometalates (POMs) covalently functionalized with methyl methacrylate groups were applied as surfactants in the emulsion polymerization reaction of styrene. Due to the copolymerization of the methyl methacrylate groups and the styrene monomers, the polyoxometalate clusters are covalently grafted onto the surface of polystyrene latex nanoparticles. Such latex particles are fully covered wit...

The synthesis of poly(VDF-co-TFMA) copolymers (where VDF and TFMA stand for vinylidene fluoride and α-trifluoromethacrylic acid, respectively) by iodine transfer polymerization without any surfactant is presented. First, the synthesis and the control of the copolymerization of VDF and TFMA were investigated in the presence of two chain transfer agents, 1-perfluorohexhyl iodide (C

Supramolecular copolymers, non-covalent analogues of synthetic copolymers, constitute a new and promising class of polymers. In contrast to their covalent counterparts, the details of their mechanism of formation, as well as the factors determining their composition and length, are still poorly understood. Here, the supramolecular copolymerization between two slightly structurally different ben...

Radical ring-opening copolymerization-induced self-assembly (rROPISA) was successfully applied to the synthesis of core-, surface- or surface plus core-degradable nanoparticles in heptane, leading site-specific degradability by rROPISA.