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Triblock Terpolymer (triblock + terpolymer)

Distribution by Scientific Domains

Polymers and Materials Science	100%

Selected Abstracts

Self-Assembled Nanoscale Ring Arrays from a Polystyrene- b -polyferrocenylsilane- b -poly(2-vinylpyridine)Triblock Terpolymer Thin Film

ADVANCED MATERIALS, Issue 37 2009
Vivian P. Chuang
Hollow ring arrays with an outer and inner diameter of 33 and 11,nm, respectively, are formed from a thin film of poly-(styrene- b -ferrocenylethylmethylsilane- b -2-vinyl pyridine) (PS- b -PFS- b -P2VP) triblock terpolymer with a core/shell cylindrical morphology. The PS minority block forms a core surrounded by a PFS shell in a P2VP matrix; the core/shell structure is oriented perpendicularly to the film surface. The PS core and P2VP matrix blocks are partly removed using oxygen reactive ion etching, leaving ring patterns made from oxidized PFS. [source]

Titanium-mediated [CpTiCl2(OEt)] ring-opening polymerization of lactides: A novel route to well-defined polylactide-based complex macromolecular architectures

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2010
Nikolaos Petzetakis
Abstract Among three cyclopentadienyl titanium complexes studied, CpTiCl2(OEt), containing a 5% excess CpTiCl3, has proven to be a very efficient catalyst for the ring-opening polymerization (ROP) of L -lactide (LLA) in toluene at 130 °C. Kinetic studies revealed that the polymerization yield (up to 100%) and the molecular weight increase linearly with time, leading to well-defined PLLA with narrow molecular weight distributions (Mw/Mn , 1.1). Based on the above results, PS- b -PLLA, PI- b -PLLA, PEO- b -PLLA block copolymers, and a PS- b -PI- b -PLLA triblock terpolymer were synthesized. The synthetic strategy involved: (a) the preparation of OH-end-functionalized homopolymers or diblock copolymers by anionic polymerization, (b) the reaction of the OH-functionalized polymers with CpTiCl3 to give the corresponding Ti-macrocatalyst, and (c) the ROP of LLA to afford the final block copolymers. PMMA- g -PLLA [PMMA: poly(methyl methacrylate)] was also synthesized by: (a) the reaction of CpTiCl3 with 2-hydroxy ethyl methacrylate, HEMA, to give the Ti-HEMA-catalyst, (b) the ROP of LLA to afford a PLLA methacrylic-macromonomer, and (c) the copolymerization (conventional and ATRP) of the macromonomer with MMA to afford the final graft copolymer. Intermediate and final products were characterized by NMR spectroscopy and size exclusion chromatography, equipped with refractive index and two-angle laser light scattering detectors. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1092,1103, 2010 [source]

Synthesis of a model cyclic triblock terpolymer of styrene, isoprene, and methyl methacrylate

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 10 2002
Dimitris Pantazis
Abstract The synthesis of a model cyclic triblock terpolymer [cyclic(S- b -I- b -MMA] of styrene (S), isoprene (I), and methyl methacrylate (MMA) was achieved by the end-to-end intramolecular amidation reaction of the corresponding linear ,,,-amino acid precursor [S- b -I- b -MMA] under high-dilution conditions. The linear precursor was synthesized by the sequential anionic polymerization of S, I, and MMA with 2,2,5,5-tetramethyl-1-(3-lithiopropyl)-1-aza-2,5-disilacyclopentane as an initiator and amine generator and 4-bromo-1,1,1-trimethoxybutane as a terminator and carboxylic acid generator. The separation of the unreacted linear polymer from the cyclic terpolymer was facilitated by the transformation of the unreacted species into high molecular weight polymers by the evaporation of the reaction solvent and the continuation of the reaction under high-concentration conditions. The intermediate materials and the final cyclic terpolymer, characterized by size exclusion chromatography, vapor pressure osmometry, thin-layer chromatography, IR and NMR spectroscopy, exhibited high molecular weight and compositional homogeneity. Dilute-solution viscosity measurements were used as an additional proof of the cyclic structure. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 1476,1483, 2002 [source]