Search results for "polymerization"
showing 10 items of 1689 documents
Poly(isoglycerol methacrylate)-b-poly(d or l-lactide) Copolymers: A Novel Hydrophilic Methacrylate as Building Block for Supramolecular Aggregates
2010
On the basis of a new acetal-protected glycerol monomethacrylate monomer (cis-1,3-benzylidene glycerol methacrylate/BGMA) a series of potentially biocompatible and partially biodegradable homo- and block copolymers were synthesized. ATRP polymerization of BGMA yielded well-defined polyacrylates with pendant benzylidene acetal groups and high glass transition temperatures (115−130 °C). This hydrophobic poly(cis-1,3-benzylidene glycerol methacrylate) could be readily transformed into the hydrophilic and water-soluble poly(1,3-dihydroxypropyl methacrylate), referred to as poly(isoglycerol methacrylate) (PIGMA). It exclusively contains primary hydroxyl groups and therefore differs significantly…
Multi-Arm Star Poly(L-lactide) with Hyperbranched Polyglycerol Core
2007
Biocompatible multi-arm star block copolymers based on poly(L-lactide) (PLLA) have been prepared by a core-first approach, using hyperbranched polyglycerol (PG), a polyether polyol, as a polyfunctional initiator. The molecular weight of the hyperbranched initiator-core was varied from 2 200 to 5 200 g mol -1 , molecular weights of the resulting multi-arm stars were in the range of 6 700-107 000 g mol -1 (NMR), depending on the amount of dilactide (LA) added. Various monomer/initiator ratios have been employed in the Sn-catalyzed LA polymerization in order to vary the length of the lactide arms from DP n (arm) = 2 to 20 units. Detailed NMR analysis using conventional and 2D-NMR techniques (e…
Molecular organization of a water-insoluble iridium(III) complex in mixed monolayers.
2007
Abstract In this work, organized mixed monolayers containing a cationic water-insoluble iridium(III) complex, Ir-dye, [Ir(ppy)2(tmphen)]PF6, (tmphen = 3,4,7,8-tetramethyl-1,10-phenanthroline, and ppy = 2-phenylpyridine), and an anionic lipid matrix, DMPA, dimyristoyl-phosphatidic acid, with different molar proportions, were formed by the co-spreading method at the air–water interface. The presence of the dye at the interface, as well as the molecular organization of the mixed films, is deduced from surface techniques such as π – A isotherms, Brewster angle microscopy (BAM) and reflection spectroscopy. The results obtained remark the formation of an equimolar mixed film, Ir-dye/DMPA = 1:1. B…
D2/H2 adsorption selectivity on FAU zeolites at 77.4 K: Influence of Si/Al ratio and cationic composition
2018
Abstract Equilibrium D2/H2 adsorption selectivity was determined at 77.4 K below 1000 hPa for a series of FAU type zeolites X exchanged with different cations (Li+, Na+, K+, Mg2+, Ca2+, Ba2+ and Mn2+). In addition NaY, DAY (dealuminated Y) and pure silica CHA and MFI zeolites were studied. Two experimental approaches were used to determine the D2/H2 adsorption selectivity: direct determination at the thermodynamic equilibrium from manometric coadsorption experiments and calculations by Ideal Adsorbed Solution Theory (IAST) from single gas adsorption isotherms. While these two approaches are not in quantitative agreement, they reveal similar trends. At low loading ( MnX > LiX > CaX ≈ NaX > …
Synthesis and X-ray Crystal Structures of (C5HiPr4)Ln(BH4)2(THF)(Ln = Nd and Sm), Versatile Precursors for Polymerization Catalysts
2000
The new half metallocenes [(C5HiPr4)Ln(BH4)2(THF)] [Ln = Sm (1) and Nd (2)], and [(C5HiPr4)U(BH4)3] (3) have been synthesized. The crystal structures of 1 and 2 and of the metallocenes [(C5HiPr4)2Ln(BH4)] [Ln = Sm (4) and Nd (5)] have been determined. The substitution of the BH4 groups of 1 and 2 by a nitrogen-based ligand is possible. In the presence of butyllithium, these complexes show an activity in isoprene and styrene polymerization.
Stereospecific Polymerization of Isoprene with Nd(BH4)3(THF)3/MgBu2 as Catalyst
2004
The neodymium trisborohydride Nd(BH 4 ) 3 - (THF) 3 (THF = tetrahydrofuran) has been used as a catalyst precursor for isoprene polymerization for the first time. Associated to an excess of Al(Et) 3 , the resulting catalyst is moderately active, giving a mixture of cis- and trans- polymer. Addition of a stoichiometric amount of MgBu 2 to Nd(BH 4 ) 3 (THF) 3 affords a stereospecific catalyst providing trans-1,4-polyisoprene, more than 96% regular. That dual component Nd/Mg system also shows a better efficiency and good control of the molecular weights. A molecular structure is tentatively attributed to a bimetallic active species, based on 1 H NMR experiments.
Group 3 and 4 metal alkyl and hydrido complexes containing a linked amido-cyclopentadienyl ligand: “constrained geometry” polymerization catalysts fo…
2002
Abstract In order to understand the nature of the putative cationic 12-electron species [M(η 5 :η 1 -C 5 R 4 SiMe 2 NR′)R″] + of titanium catalysts supported by a linked amido-cyclopentadienyl ligand, several derivatives with different cyclopentadienyl C 5 R 4 and amido substituents R′ were studied systematically. The use of tridentate variants (C 5 R 4 SiMe 2 NCH 2 CH 2 X) 2− (C 5 R 4 =C 5 Me 4 , C 5 H 4 , C 5 H 3 t Bu ; X=OMe, SMe, NMe 2 ) allowed the NMR spectroscopic observation of the titanium benzyl cations [Ti(η 5 :η 1 -C 5 Me 4 SiMe 2 NCH 2 CH 2 X)(CH 2 Ph)] + . Isoelectronic neutral rare earth metal complexes [Ln(η 5 :η 1 -C 5 R 4 SiMe 2 NR′)R″] can be expected to be active for pol…
Effect of the remaining lanthanide catalysts on the hydrolytic and enzymatic degradation of poly-(ε-caprolactone)
2003
Poly-(e-caprolactone) is a biodegradable polymer, which can be used for both medical and environmental applications. Due to its multiple applications the synthesis of such a polymer has been attracting an increasing attention in the past few decades. In our work, the polymers were synthesised by bulk polymerisation, using different lanthanide halides as initiators. The lanthanide derivatives are known as very active catalysts in the ring-opening polymerisation of cyclic esters. Moreover, they are not toxic in comparison of catalysts, which are usually used for this synthesis. In this paper, the influence of the lanthanides on both the hydrolytic and enzymatic degradation of the PCL obtained…
Neutral and cationic trimethylsilylmethyl complexes of the rare earth metals supported by a crown ether: synthesis and structural characterization
2003
The synthesis of a series of thermally robust, isolable trimethylsilylmethyl complexes of the rare earth metals stabilized by 12-crown-4 [Ln(CH2SiMe3)3(12-crown-4)] (Ln = Sc, Y, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) is reported. The crystallographically characterized yttrium and lutetium complexes [Ln(CH2SiMe3)3(12-crown-4)] exhibit facial coordination of the crown ether at the neutral lanthanide trialkyl unit. The coordination geometry can be derived from a capped octahedron. VT NMR spectroscopic studies revealed a labile coordination of the crown ether in thf solution. Reaction of the diamagnetic derivatives with triethylammonium tetraphenylborate in thf results in the clean formation of th…