Search results for "plastics"

Connectivity Defects and Collective Assemblies in Model Metallo‐Supramolecular Dual‐Network Hydrogels

2019

Formation and Characterization of Self-Assembled Films of Thiol-Derivatized Poly(Dimethylsiloxane) on Gold

1997

Poly(dimethylsiloxane) (PDMS) copolymers containing propanethiol side chain “stickers” for forming self-assembled films on gold surfaces have been studied by various experimental techniques including ellipsometry, contact angle measurements, FT-IR, angle-dependent XPS, and ToF−SIMS. The results show that the thiol-containing side chains do not all chemisorb to the gold surfaces. In addition, the concentration of these sticker units was found to have a dominant effect on the polymer film thickness, the surface wetting properties, and the orientation of the PDMS backbone. Ab initio calculations reveal that the IR-active PDMS Si−O stretching bands can be used as indications of chain orientatio…

An All-ROMP Route to Graft Copolymers

2007

A new versatile synthesis strategy for macromonomers has been developed that uses the living ring-opening metathesis polymerization (ROMP) with commercial Grubbs first generation ruthenium initiators. Homopolymers as well as diblock copolymers were end-functionalized with norbornene derivatives to serve as macromonomers. The graft copolymerization of the macromonomers was also carried out employing ROMP. Well-defined and highly functional graft copolymers are accessible by this new synthetic route.

RAFT Polymerization of Pentafluorophenyl Methacrylate: Preparation of Reactive Linear Diblock Copolymers

2005

Reversible addition fragmentation chain transfer (RAFT) polymerization of pentafluorophenyl methacrylate (PFMA) was carried out in the presence of cumyldithiobenzoate and 4-cyano-4-((thiobenzoyl)sulfanyl)pentanoic acid, respectively. These chain transfer agents with 2,2'-azoisobutyronitrile (AIBN) as initiator yielded the active ester polymer poly(PFMA) with M n up to 17000 g . mol -1 and low polydispersity index (M w /M n <1.2). Kinetic analysis using 19 F NMR spectroscopy and gel permeation chromatography (GPC) measurements showed controlled polymerization behavior for both chain transfer agents. Successful preparation of linear diblock copolymers consisting of an active ester block and m…

Amphipolar Core−Shell Cylindrical Brushes as Templates for the Formation of Gold Clusters and Nanowires

2002

Methacryloyl end-functionalized block copolymers consisting of styrene and vinyl-2-pyridine were polymerized to poly(block co-macromonomer)s with a much higher main chain than side chain degree of ...

Local and Subchain Relaxation of Polyisoprene in Multiblock Copolymers with a Tapered Interface

2020

We report on the local and (sub-) chain dynamics in a new class of tapered multiblock copolymers synthesized by the repeated statistical living anionic copolymerization of a mixture of isoprene and...

Synthesis of a polystyrene-arm-polybutadiene-arm-poly(methyl methacrylate) triarm star copolymer

1996

The straightforward synthesis of a polystyrene-arm-polybutadiene-arm-poly(methyl methacrylate) triarm star copolymer has been successfully realized by a sequence of reactions which involves the sequential addition of a living polybutadienyllithium to a polystyrene macromonomer with a terminal 1,1-diphenylethylene unit and subsequent polymerization of methyl methacrylate. The high-molecular-weight polystyrene-arm-polybutadiene-arm-poly(methyl methacrylate) star copolymer shows microphase separation into three phases.

Synthesis of Amphiphilic Block Copolypept(o)ides by Bifunctional Initiators: Making PeptoMicelles Redox Sensitive.

2015

In this work, the synthesis of polypeptoid-block-polypeptide copolymers (block copolypept(o)ides) based on bifunctional initiators is described, which introduces a distinct chemical entity at the connection between both blocks. With a view towards redox-sensitive block copolypept(o)ides, a cystamine-based initiator was used to synthesize polysarcosine macroinitiators with degrees of polymerization (Xn) between 100 and 200 displaying monomodal molecular weight distributions and dispersities (Đ) around 1.1 as determined by size exclusion chromatography. Block copolypept(o)ides with a poly(γ-t-butyloxycarbonyl-L-glutamate) (PGlu(O(t) Bu)) block (Xn = 25 or 50) were synthesized by controlled N-…

Critical Micelle Concentration of Micelles with Different Geometries in Diblock Copolymer/Homopolymer Blends

2011

Summary In this paper, we have investigated the shape transition ofanisolatedmicelleformedintheAB-diblockcopolymerandA-homopolymer blends. SCFT has been employed tocompute the CMC for three different morphologies:lamellar, cylindrical and spherical. By comparing theCMC for different shapes, we can determine the preferredmicelle geometry. Several factors can influence the micellemorphology,andwehaveexploredtheeffectsofthediblockasymmetry, the homopolymer/copolymer length ratio andthe monomer–monomer interaction, on the micelle shapetransitions. It is found the micelle undergoes a sequenceof shape transitions, lamellar ! cylindrical ! spherical,when the A-block of the copolymer becomes longer.…

Rheology of a Lower Critical Solution Temperature Binary Polymer Blend in the Homogeneous, Phase-Separated, and Transitional Regimes

1996

Small amplitude oscillatory shear rheology is employed in order to investigate the linear viscoelastic behavior of the lower critical solution temperature blend polystyrene/poly(vinyl methyl ether), PS/PVME, as a function of temperature and composition. At low temperatures, where the mixture is homogeneous, the dependence of the zero shear viscosity (η0) on concentration is measured and is well-described by means of a new mixing rule, based on surface fractions instead of volume fractions. Shift factors from time-temperature superposition (TTS) exhibit a Williams−Landel−Ferry (WLF) behavior. As the macrophase separation temperature is approached (the phase diagram being established by turbi…