Polyaniline nanostructures (nanosheets, nanofibers, and nanoparticles) can be assembled at the organic/aqueous interface or in solution by controlling the diffusion rate and the polymerization induction time of aniline. The quality of polyaniline nanostructures is determined by the polymerization solution conditions. Polyaniline nanosheets formation mechanism was proposed. Under certain polymerization conditions, polyaniline nanofibers or/and nanoparticles were obtained.
Summary: Polypyrrole nanotubes with high electric conductivity and azo function have been fabricated in high yield via an in‐situ polymerization. During the process fibrillar complex of FeCl3 and methyl orange (MO), acting as a reactive self‐degraded template, directed the growth of polypyrrole on its surface and promoted the assembly into hollow nanotubular structures.
TEM image of uncompleted PPy nanotubes synthesized in MO solutions after reaction for 40 min. 相似文献
Summary: Polyaniline‐vanadium oxide nanocomposite nanosheets with thickness between 10 and 20 nm, and lateral dimensions in the range of hundreds of nanometers to several microns have been synthesized by in situ intercalation polymerization of aniline with layered V2O5 under hydrothermal conditions. The product was characterized by field‐emission scanning electron microscopy (FE‐SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT‐IR) spectroscopy, and X‐ray diffractometer (XRD). The effects of the concentration of aniline and reaction temperature on the morphologies of polyaniline‐vanadium oxide nanocomposites have also been investigated.
SEM image of tremella‐like polyaniline‐vanadium oxide nanocomposite nanosheets. 相似文献
FTIR microspectrometry with in situ temperature variation and IR‐peak‐mapping capability, and POM characterization were used to study the crystal distribution in dual spherulites in poly(heptamethylene terephthalate). By tracing the crystalline IR bands of the α‐crystal and β‐crystal to get the crystal distribution, the techniques resolve that the ringed and ringless spherulites comprise α‐ and β‐crystals, respectively. In addition, temperature‐dependent IR analyses on the spots related to the two crystals also reveal the α‐ and β‐crystals melt at 98 and 104 °C, respectively. The ringed and ringless spherulites were proven to be correlated with the α‐ and β‐crystal forms, respectively.
Amphiphilic polymer brushes grafted onto gold nanoparticles impart distinct solvent‐responsive behavior via the change to particle size and surface chemistry and, therefore, wide application prospects can be expected. Coarse‐grained simulations are performed for block and/or mixed polystyrene (PS)/poly(ethylene oxide) (PEO)‐modified amphiphilic gold nanoparticles (AuNP) to investigate their responsive behavior in five different solvents by analyzing their morphology, distribution density profiles, and gyration radii. Typical core–shell, Janus‐type, buckle‐like, ring‐like, jellyfish‐like, and octopus‐like morphologies are formed. Influence of block sequence, mixing mode, and several other effects are discussed. Responsive particle size and surface hydrophilicity can be successfully reproduced by altering solvents.
This feature article briefly highlights some of the recent advances in polymers in which phosphorus is an integral part of the backbone, with a focus on the preparation of functional, highly branched, soluble polymers. A comparison is made between the related families of materials polyphosphazenes, phosphazene/phosphorus‐based dendrimers and polyphosphoesters. The work described herein shows this to be a rich and burgeoning field, rapidly catching up with organic chemistry in terms of the macromolecular synthetic control and variety of available macromolecular architectures, whilst offering unique property combinations not available with carbon backbones, such as tunable degradation rates, high multivalency and facile post‐polymerization functionalization. As an example of their use in advanced applications, we highlight some investigations into their use as water‐soluble drug carriers, whereby in particular the degradability in combination with multivalent nature has made them useful materials, as underlined by some of the recent studies in this area.
A generalized silica coating scheme is used to functionalize and protect sub‐micron and micron size dicyclopentadiene monomer‐filled capsules and polymer‐protected Grubbs' catalyst particles. These capsules and particles are used for self‐healing of microscale damage in an epoxy‐based polymer. The silica layer both protects the capsules and particles, and limits their aggregation when added to an epoxy matrix, enabling the capsules and particles to be dispersed at high concentrations with little loss of reactivity.
A rod‐coil block copolymer consisting of poly(3‐hexylthiophene) (P3HT) and poly(N‐vinylcarbazole) (PVK) ( P3HT‐ b ‐PVK ) in a single molecular architecture is prepared as the first example for WOLEDs. By obtaining the phase separated domains in thin film of the resulting block copolymer, it is possible to suppress energy transfer from PVK as wide bandgap units to P3HT as low bandgap blocks, yielding dual emissions for white electroluminescence with CIE coordination of (0.34, 0.33).
Polyaniline‐polypyrrole (PANI‐PPy) nanofibers with high aspect ratios have been synthesized by a one‐step, surfactant‐assisted chemical oxidative polymerization from mixtures of aniline (An) and pyrrole (Py) monomers. PANI‐PPy nanofibers synthesized with an excess of either PANI or PPy show similar spectral (UV‐vis and FT‐IR) characteristics as the individual homopolymers, whereas nanofibers from an equimolar mixture of An and Py display unique spectral characteristics. PANI‐PPy nanofibers undergo a spontaneous redox reaction with metal ions to produce metal nanoparticles with various morphologies and/or sizes. These findings may open new opportunities for synthesizing functional polymer nanofibers and metal nanoparticles with controllable sizes and/or morphologies.
Perfectly alternating copolymers can be synthesised by reacting diacrylates with terminal dienes using alternating diene metathesis polycondensation (ALTMET). This novel method is very versatile and allows preparation of diverse structures of polymers, including main‐chain liquid crystalline polymers.
Main‐chain liquid crystalline polymer obtained by ALTMET. 相似文献
Large scale of well‐ordered macroporous π‐conjugated polymer monoliths have been successfully prepared through a new approach using micrometer‐sized naphthalene crystals as templates. The macroporous monoliths of poly(p‐phenylenevinylene) (PPV) and poly(p‐phenyleneethynylene) (PPE) grew along the unidirectional freezing direction inside the template naphthalene crystals which lead to the formation of controlling morphologies and homogeneous diameters. The polymer monoliths show straight and lamella macroporous structures. The diameters of pores and the thickness of pore walls can be controlled by tuning the freezing temperature.
A new chromophore, C1 , based on a similar DπA‐structure as in the FTC ‐chromophore but with a hydroxyalkyl spacer perpendicular to the direction of the dipole moment was synthesized. Both chromophores and the CLD ‐chromophore were used to prepare high Tg nonlinear optical vinyl polymers. The influence of the position of the spacer on the DπA‐system on the NLO response of the resulting polymers was investigated.
Summary: We describe a way to obtain biomimetic, hierarchical surface morphologies. In order to mimic natural surfaces more accurately such as lotus leaves and gecko feet, we employ a strategy that bears many of the attractive characteristics of natural materials synthesis. The system in question consists of a photocurable monomer and water. To this quasi‐two‐component system we add polymer latex spheres. The monomer–water interface is then manipulated according to the well‐established science of complex fluids. Drawing from the rich phase behavior of particle‐stabilized emulsions, we demonstrate the creation of complex biomimetic morphologies over many length scales. The resulting structures are then solidified by crosslinking the monomer with UV light.
Comparison of an AFM image of a PMMA colloidosome assembly with that of the textured surface of a superhydrophobic Hygoryza aristata leaf (inset). 相似文献
Functionalizing and controlling nanostructures resulting from block copolymer self‐assembly are key factors in defining their application. In this work, a simple but quite general route to achieve both goals simultaneously is discussed. In thin films of polystyrene‐block‐poly(vinyl pyridine) (PS‐b‐PVP) with small concentrations of a gold salt, the salt is found to complex with the PVP block which leads to an orientation of the microdomains normal to the surface after solvent annealing together with functionalization. By increasing the amount of gold salt, on the other hand, micelles are found to form in solutions leading to a range of different morphologies in the thin films.
One‐dimensional methyl orange fibrils can be easily prepared. They are stable in acidic aqueous solutions and soluble in neutral water. When used to synthesize conducting polymer microtubules, the fibrils act as “hard templates” formally but as “soft templates” effectively. Microtubular structures of polypyrrole, polyaniline, and poly(3,4‐ethylenedioxythiophene) have been achieved successfully via such water‐soluble versatile templates.
While network‐like assemblies are formed by amphiphilic polyphosphazenes with poly(N‐isopropylacrylamide) and ethyl tryptophan as side groups in aqueous solution, a significant morphology transformation is observed when small molecules that exhibit hydrogen‐bonding interactions with amphiphilic copolymers are introduced during the preparation of polymeric assemblies through a dialysis procedure. Depending on copolymer composition and the content of small molecules introduced, aggregates ranging from general vesicles, high‐genus vesicles, to well‐defined nanospheres can be prepared successfully as clearly evidenced by TEM observation, which suggests this procedure should be a novel approach to prepare composite vesicles.
