Degradable dendrimer‐like PEOs were designed using an original ABC‐type branching agent featuring a cleavable ketal group, following an iterative divergent approach based on the anionic ring opening polymerization (AROP) of ethylene oxide and arborization of PEO chain ends. A seventh generation dendrimer‐like PEO carrying 192 peripheral hydroxyls and exhibiting a molar mass of 446 kg · mol−1 was obtained in this way. The chemical degradation of these dendritic scaffolds was next successfully accomplished under acidic conditions, forming linear PEO chains of low molar mass (≈2 kg · mol−1), as monitored by 1H NMR, SEC, and MALDI‐TOF mass spectrometry as well as by AFM.
Summary: Tetraaniline‐block‐poly(L ‐lactide) diblock oligomers are synthesized via ring‐opening polymerization. The diblock oligomers cast from an L ‐lactide selective solvent (chloroform) show spherical aggregates for the leucoemeraldine state, and ring‐like structures that are composed of much smaller spherical aggregates for the emeraldine state. The formation mechanisms of the two different surface morphologies are discussed in detail.
Surface morphology changes induced by oxidation of the aniline segment of tetraaniline‐block‐poly(L ‐lactate) and drying effects. 相似文献
Summary: Bisphenol A solid epoxy serves as an effective reaction compatibilizer to the bisphenol A polycarbonate (PC)/PMMA bilayer systems. Addition of epoxy to the bottom PMMA layer can retard or even prevent the dewetting of PC films by introducing crosslinking between both components at the interface. This is the first investigation of polymer bilayers stabilized by chemical reactions.
AFM topographic image of a representative dewetting hole. 相似文献
A facile one‐step method has been developed to prepare both superhydrophobic and superoleophilic surfaces of polystyrene (PS) without any chemical modification. A rough film consisting of micro‐bead and nano‐fiber mixed structures is formed by spraying a PS solution onto a large area and any type of substrate. The mixed structures with such unique wettability properties can be used in oil/water separation and as oil sorbents.
Tertiary amines were found to remarkably enhance the catalytic activity of ATRP catalysts CuBr/tris[(2‐pyridyl)methyl]amine and CuBr/tris[2‐(dimethylamino)ethylamine]. These two catalysts alone failed to polymerize MA, MMA, and styrene at reduced catalyst concentrations. With tertiary amines such as triethylamine both catalysts could mediate fast polymerizations of the three monomers in a controlled manner at as low as 1 mol‐% catalyst relative to initiator. A mechanism study showed that tertiary amines reduced copper(II) complexes to active copper(I) complexes.
A fast method is presented for the calculation of the MSD and the MWD of polymers obtained via step‐growth polymerization of polyfunctional monomers bearing identical reactive groups (i.e., systems of type “Afi”). Using this method, the complete distribution can be calculated rapidly, not just the statistical averages of the polymer population such as or . The computed MSD and MWD give more insight than these averages and can be compared to similar data measured on actual polymer systems. The low‐ and intermediate molecular size/weight part of the distribution curves are calculated using a recurrence scheme, while the high‐molecular tail (large and very large polymers) of the distributions is derived from an asymptotic approximation of the associated generating functions.
Summary: The first example of a room temperature reversible addition‐fragmentation chain transfer polymerization conducted directly in aqueous media is detailed. Under these conditions acrylamide and N,N‐dimethylacrylamide may be polymerized in a controlled fashion to near quantitative conversions employing a difunctional trithiocarbonate chain transfer agent (CTA). Hydrolysis studies conducted at pH 5.5 suggest that the CTA is stable up to approximately 50 °C.
Cystamine, when employed as a cross‐linking agent, leads to poly(amidoamine) networks, which on reaction with 2,2′‐dithiodipyridine turn into linear poly(amidoamine)s with side dithiopyridyl groups that easily undergo exchange reactions with reduced L ‐glutathione, a model thiol‐containing biologically active peptide. The resultant products represent the first examples of soluble poly(amidoamine)–peptide conjugates in which the peptide moieties are linked to the polymer chain by S S bonds stable in blood, but cleavable inside cells.
An enzymatic tandem reaction is described in which the enzymes phosphorylase and Deinococcus geothermalis glycogen branching enzyme (Dg GBE) catalyze the synthesis of branched polyglucans from glucose‐1‐phosphate (G‐1‐P). Phosphorylase consumes G‐1‐P and polymerizes linear amylose while Dg GBE introduces branching points on the α‐(1 → 6) positions by reshuffling short oligosaccharides. The resulting branched polyglucans have an unusually high degree of branching of 11%.
The mechanistic interpretation of kinetic anomalies in reversible addition–fragmentation chain transfer (RAFT)‐mediated polymerization is critically reviewed. The main conclusion of this exercise is that available data do not allow model discrimination between the two prevailing mechanistic schemes, i.e., the slow fragmentation model and the intermediate radical termination model. However, assessment of the rate parameters reveals that the incompatibilities may not be as large as previously reported in literature. Dedicated kinetic studies on model compounds should be performed to shed further light on the seemingly incompatible data that currently exists in literature.
A new semi‐analytical approach to model simultaneous chain scission and branching is described that assumes the separation of the scission and the branching problem. The required properties of the linear segments or primary polymers forming the branched architectures are found by a kinetic model. The general rules for the construction of branched architectures from populations of linear segments then lead to an analytical expression for the branching distribution and a semi‐analytical expression for the bivariate length/branching distribution. The method is applied to the scission of an initially branched polymer and subsequent terminal branching on scission points and activated terminal double bonds. Exact agreement is found with Monte Carlo sampling results.
Summary: Monodisperse thermosensitive PS‐NIPA core‐shell particles composed of a PS core and a cross‐linked PNIPA shell can be successfully synthesized by a novel method: photoemulsion polymerization. Cryo‐TEM images indicate clearly the core‐shell morphology of the PS‐NIPA particles: A homogeneous regular PNIPA shell has been affixed on the spherical PS core. DLS measurements indicate that the obtained PS‐NIPA latex particles are thermosensitive. The shell of PNIPA networks with different cross‐linking densities can shrink and re‐swell with temperature and the volume transition temperature is around 32 °C in all cases.
Cryo‐TEM image of PS‐NIPA core‐shell particles. 相似文献
This review covers the literature concerning the modification of polysaccharides through controlled radical polymerizations (NMP, ATRP and RAFT). The different routes to well‐defined polysaccharide‐based macromolecules (block and graft copolymers) and graft‐functionalized polysaccharide surfaces as well as the applications of these polysaccharide‐based hybrids are extensively discussed.
Multicomponent phase change microfibers, which can storage and release thermal energy in a stepwise manner, are firstly prepared through a facile one‐step multifluidic compound‐jet electrospinning with temperature control. The multiresponsive effect benefits from a special multichannel tubular microstructure that could controllably encapsulate different phase change materials into the channels independently. Aside from the fabrication of multicomponent phase change microfibers, the melt multifluidic compound‐jet electrospinning is promising for applications related to microencapsulation and multifunctional material fields.
