Furan ring‐functionalized solid surfaces are achieved by the initiated chemical vapor deposition (iCVD) method, a solvent‐free process to form films under mild conditions. The polymerization of furfuryl methacrylate monomer is initiated by a resistively heated filament wire. The functionality of the furan group in the iCVD film enabled Diels–Alder chemistry with 4‐phenyl‐1,2,3‐triazolin‐3,5‐dione (N‐PTD).
Summary: A water‐soluble gold nanoparticle aggregate 2 was prepared by chloroauric acid and a polypseudorotaxane 1 of mono‐6‐thio‐β‐cyclodextrin with poly(propylene glycol) bis(2‐aminopropyl ether) ( ≈ 2 000) in the presence of sodium borohydride in N,N‐dimethylformamide (DMF) solution. The investigative results indicated that the gold nanoparticle aggregate 2 might act as an efficient DNA‐cleavage reagent.
A typical TEM image of gold nanoparticle aggregate 2 . 相似文献
The use of the molecular imprinting technique to produce polymers with high specificity for a given “molecular template” has undergone a rapid and expansive evolution since the inception of the idea over half a century ago. It was only a matter of time before the seemingly inevitable “marriage” of this concept with another modern research obsession, the generation of “smart” polymers, capable of reacting quickly, accurately and reproducibly to changes in their environment. Many advances have since been made, concerning the quality and diversity of these systems and polymers responsive to temperature, pH and a host of other environmental cues now exist. This article provides a succinct overview of the process and outcomes of “smart” molecular imprinting, followed by a detailed assessment of recent developments and applications in such field.
Supramolecular poly(vinyl acetate) PVAc 3‐arms stars were successfully generated by Reversible Addition–Fragmentation chain Transfer (RAFT)‐polymerized chains bearing hydrogen‐bonding heterocomplementary associating units. Chain Transfer Agents (CTA) bearing thymine‐ and diaminopyridine‐based units were first synthesized and proved to mediate efficiently the polymerization of VAc. The binding ability of the chains in solution was then demonstrated by 1H NMR and GPC measurements, proving the formation of the supramolecular stars.
We report a facile method to accomplish the crosslinking reaction of PVA with SWNTs, MWNTs, and C‐60 using MW irradiation. Nanocomposites of PVA crosslinked with SWNT, MWNT and C‐60 were prepared expeditiously by reacting the respective carbon nanotubes with 3 wt.‐% PVA under MW irradiation, maintaining a temperature of 100 °C, representing a radical improvement over literature methods to prepare such crosslinked PVA composites. This general preparative procedure is versatile and provides a simple route to manufacture useful SWNT, MWNT and C‐60 nanocomposites.
Green nanocomposite coatings based on renewable plant oils have been developed. An acid‐catalyzed curing of epoxidized plant oils with 3‐glycidoxypropyltrimethoxysilane produced transparent nanocomposites. The hardness and mechanical strength improved by incorporating the silica network into the organic polymer matrix, and good flexibility was observed in the nanocomposite. The nanocomposites showed high biodegradability.
Summary: The vapor‐based synthesis and characterization of a reactive polymer, poly[(4‐formyl‐p‐xylylene)‐co‐(p‐xylylene)] ( 1 ), have been reported. The reactive polymer coating enables the immobilization of oligosaccharides via the chemoselective aldehyde‐hydrazide coupling reaction.
Summary: A drop‐on‐demand ink‐jet printer has been used to print a silver‐organic solution onto glass substrates. Conductive silver tracks were obtained by heat treatment of the ink‐jet printed deposits at temperatures ranging from 125 °C–200 °C in air. Resistivity values were found to have dropped to two to three times the theoretical resisitivity of bulk silver after temperatures of 150 °C and above were used.
A novel α,ω‐heterofunctional poly(ethylene oxide) (PEO) macromonomer possessing methacryloyl and thienyl end groups was prepared by ring‐opening polymerization of ethylene oxide initiated by potassium thienylethoxide and termination of the living PEO ends with methacryloyl chloride. Incorporation of methacryloyl and thienyl groups was confirmed by free‐radical and oxidative polymerization processes, respectively, and by means of 1H NMR analysis.
Summary: We describe a simple photochemical process that allows the covalent attachment of a variety of different polymers at room temperature onto aluminium surfaces. The system is based on a photoreactive benzophenone derivative that is bound to aluminium surfaces by a phosphonic acid anchor. The synthesis of the phosphonic acid is described and the immobilization of this compound is studied by X‐ray photoelectron and FT‐IR spectroscopy. After deposition of the polymeric coating, UV light illumination at 365 nm, and solvent extraction of the substrate, polymer monolayers are obtained that are chemically bound to the surface.
Covalent attachment of polymers to the aluminium‐bound benzophenone phosphonic acid. 相似文献
Population balance equations in terms of generating functions (GF) are used to predict chain length distributions (CLD) of linear and non‐linear ideal controlled radical polymerization (CRP) systems. It is here shown that under simplified conditions analytical solutions for the CLD can be found and moreover the fundamental CLD derived by H. Tobita in 2006 is a limiting case of the more general solutions here presented. In order to deal with more complex CRP systems, solutions based upon the numerical inversion of GF are presented. These studies are also extended to the non‐linear CRP of vinyl/divinyl monomers where multimodal CLDs are predicted to occur.
We report for the first time the preparation of single polypyrrole (PPy) molecule chains using a “metal‐organic framework” with 1 nm channels as a template. The obtained one‐dimensional (1‐D) PPy has highly structure order and excellent conductivity, which has improved by as much as five orders of magnitude in comparison with that of 2‐D PPy.
Well‐defined poly(ethylene oxide)s (PEOs) bearing reactive sites regularly distributed along the chain have been synthesized by the polycondensation of PEO containing a central tertiary amino group with dichloromethane, followed by quaternization with suitable reagents to obtain polyzwitterionic or cationic PEOs with alkyl, allyl, or fluorocarbon pendant groups. The pendant allyl groups have been converted into primary amino groups by reaction with 2‐aminoethanethiol hydrochloride to obtain polyamino‐functionalized PEO.
Polyfunctional PEOs bearing different pendant groups. 相似文献
Summary: A class of new, soluble, π‐conjugated polymers containing a fumaronitrile unit in the main chain were synthesized by the reaction between di(4‐bromophenyl)fumaronitrile and bis(2,2‐dimethylpropane‐1,3‐diyl)‐1,4‐dialkoxyphenylene‐2,5‐diborate employing palladium catalysts. All the polymers were photoluminescent and electrochemically active.
The new soluble π‐conjugated polymers 1a – d with photoluminescence and electrochemical activity synthesized here. 相似文献
Summary: We describe an interesting approach to the fabrication of wettability gradients from hydrophobicity to superhydrophobicity in low‐density polyethylene (LDPE) films by first forming high porosity surfaces and placing the specimens onto linear temperature gradients. While the polymer chosen for the study is non‐polar, its microporous layer provides sufficient superhydrophobicity. Lateral gradient heating of the layer results in partial melting of the polymer and correspondingly decreases porosity thus decreasing hydrophobicity.
13C solid‐state exchange NMR is applied to study the influence of morphology on chain diffusion between crystalline and noncrystalline regions in ultrahigh molecular weight linear polyethylene (PE). Lamellar‐doubling reduces the exchange rate by a factor of two indicating that the chain diffusion coefficient is largely independent of the lamellar thickness. This is discussed in terms of molecular processes in the crystallites leading to chain diffusion, confirming that the role of defects is minor compared to helical jumps of extended stems. Hindrance of the chain diffusion resulting from chain entanglements was only observed after the chains diffuse over long distances. Moreover, the role of the interphase between the noncrystalline and the crystalline regions on chain diffusion is discussed.
We report syntheses of phenylene‐, biphenylene‐, and terphenylene‐layered polymers with a xanthene scaffold by the modified Suzuki‐Miyaura coupling reaction. Their optical properties were studied in detail. The polymer end‐capped by nitrobenzene units, which act as fluorescence quenchers, exhibited the photo‐excited energy transfer from the layered oligophenylenes to the terminal units.
A novel top‐surface imaging process was successfully established using selective chemisorption of amine‐functionalized poly(dimethyl siloxane) onto the carboxylic groups formed on the surface of diazoketo‐functionalized polymer film by UV light irradiation. The chemisorbed poly(dimethyl siloxane) worked as an efficient etch mask for the subsequent oxygen plasma etching process for pattern generation. High‐resolution patterns were resolved with the new imaging process.
Summary: Amphiphilic graft polyphosphazenes (EtTrp/PNIPAm‐PPP) with different mole ratios of hydrophobic groups to hydrophilic segments were synthesized by ring‐opening polymerization and subsequent substitution reactions. The self‐assembly behavior of these graft copolymers was studied in detail by TEM, SEM, CLSM, and AFM. Depending on the copolymer composition and common organic solvent employed in dialysis process, supramolecular aggregates ranging from network, nanospheres, high‐genus particles to macrophage‐like aggregates were produced with graft copolymers.
