The properties of an oligomeric cyanate ester polymer were modified by the addition of 0.01–3 wt.‐% multi‐walled carbon nanotube (MWNT) containing particles. The dynamic mechanical behavior and thermal properties of the cyanate ester/MWNT nanocomposites were evaluated. The storage modulus, G′, of the nanocomposite with 1 wt.‐% MWNT particles was nearly 60 and 600% higher than the neat polymer at 100 and 200 °C, respectively. The glass transition temperature of the nanocomposite was also raised by 30 °C and its thermal stability in air and nitrogen was increased by 58 and 25 °C, respectively. The property improvements are attributed to reinforcement of the cyanate ester as a result of good nanotube dispersion and effective polymer‐MWNT interaction.
A simple, economical and high yielding method to prepare poly(1,4‐dihexyloxybenzene), an alkylated derivative of poly(para‐phenylene) (PPP), is reported. We further prepared a composite of poly(1,4‐dihexyloxybenzene) and CdS nanoparticles and studied their structural, optical, stability and transport properties. It was observed that the conductivity of poly(1,4‐dihexyloxybenzene) increased by several orders of magnitude when doped with CdS nanoparticles. Similarly, CdS nanoparticle‐doped PPP showed higher thermal stability, when compared to the neat polymer. As these composites could be processed in the same way as organic polymers, they would find applications in many low‐cost optoelectronic devices.
In this paper the influence of the hyperbranched polyester based on 4,4‐bis(4‐hydroxyphenyl)valeric acid on the properties of an ester diol oligomer will be discussed. The hyperbranched polyester was added to an ester diol in different amounts and the resulting bulk viscosity values were measured. Surprisingly, the resulting viscosity depends on the mixing temperature of both substances. Glass transition temperatures gave an idea about the phase behavior in the blend. H bond formation in the ester diol was intensively studied by temperature dependent IR measurements. The weakening of H bonds in the ester diol oligomer with increasing temperature was proven by IR measurements and correlates with results from viscosity measurements. These changes allow increased interactions between the ester diol and the hyperbranched polyester which causes different viscosity values depending on the mixing temperature. The overall changes in the behavior of the mixture were proven by temperature dependent AFM measurements.
Frequency dependent viscosity measurement for the mixture containing of 20 wt.‐% of the hyperbranched polyester. 相似文献
Summary: A series of poly(ether ester)s containing amide and carbamate groups as H‐bonding units and 13–50 mol‐% of poly(ethylene glycol) (PEG) segments were prepared by polycondensation in bulk using Ti(OBu)4 as a catalyst. The copolymers were obtained starting from PEG/1,4‐butanediol mixtures and a synthetic monomer carrying H‐bonding groups. These polymers were designed for biomedical applications, where material biodegradability is required. The influence of the nature of the H‐bonding units, the length of the polymethylene spacer between the H‐bonding groups and the PEG content on the thermal and solubility properties of the copolymers was investigated. Amide‐containing copolymers were more thermally stable than those containing carbamate groups. The PEG content also slightly affected the polymer thermal stability. The DSC traces of all samples presented multiple transitions, whose shape and peak temperature were strongly dependent on the PEG content. Polymer hydrophilicity, surface free energy and equilibrium swelling in phosphate buffer solution (PBS) at 37 °C were mainly influenced by the PEG content, whereas the nature of the H‐bonding groups had little effect.
Photo‐crosslinkable side‐chain liquid‐crystalline polymers (LCPs) containing photoreactive benzophenone cores are synthesized in order to obtain their corresponding side‐chain liquid‐crystalline elastomers (LCEs). This strategic synthesis allows thin elastomeric films and their integration into microsystems for actuators and micromachines to be obtained. As an example of this principle, a gripper was developed. The position of its arms can be changed by applying voltages from 1.5 to 3.5 V at different rates. Small changes in the liquid‐crystalline elastomer film cause strains of up to 150% in the microdevice and the capacity to move up to 400 times its own mass due to the nematic‐to‐isotropic transformation.
Summary: Solid‐state olefin metathesis of rigid‐rod acyclic diene metathesis (ADMET) polymers and ring‐closing metathesis (RCM) have been investigated. 1,4‐Dipropoxy‐2,5‐divinylbenzene ( 4 ) was synthesized and used in a bulk ADMET polymerization to produce oligomers of dialkoxy poly(phenylene vinylene). The reaction was continued in the solid state, effectively doubling the molecular weight. Solid‐state RCM was investigated with a variety of solid dienes and metathesis catalysts, and demonstrated in low conversions using amide diene 5 with catalysts 9 , 13 , and 14 .
A synthetic route that allows modification of 1‐vinyl‐2‐pyrrolidone with an alcohol or thiol group in its 3‐position in a one‐pot reaction without using protecting groups is described. The strategy used to achieve this goal is the reaction of the carboxamide anion of 1‐vinyl‐2‐pyrrolidone with cyclic precursors of these functionalities. It is furthermore shown that VP‐monomers functionalized with OH groups are suitable for the preparation of the corresponding copolymers with pure VP. As a second application of the new compounds, we also describe the synthesis of the first asymmetric crosslinker based on VP.
A new dithienyl benzotriazole‐based conjugated polymer was synthesized by Suzuki coupling reaction. The polymer was found to be soluble in common organic solvents, such as chloroform, tetrahydrofuran and chlorobenzene, with excellent film‐forming properties. The structure of the polymer was confirmed by 1H NMR, the molecular weights determined by GPC and the thermal properties investigated by TGA and DSC. The polymer films exhibited an absorption band in the wavelength range 300 to 610 nm. Preliminary photovoltaic cells based on the composite structure of indium tin oxide (ITO)/PEDOT:PSS/ PCDTBTz:PC 60 BM (1:2 w/w)/Al showed an open‐circuit voltage of 0.92 V, a power conversion efficiency of 2.2% and a short circuit current of 5.33 mA cm?2.
Thermo‐ and photosensitive gold nanoparticles (AuNPs) coated with an azobenzene‐contained P(DMA‐PAPA‐MAEL) copolymer are prepared by ligand exchange reactions. The photoisomerization of azobenzene moiety on the surface of P(DMA‐PAPA‐MAEL)‐coated AuNPs is detected by means of UV‐Vis spectroscopy with the presence or absence of free α‐cyclodextrin. When subjected to visible and UV light irradiation alternately, P(DMA‐PAPA‐MAEL)‐coated AuNPs in the presence of free α‐CD display a light‐tunable lower critical solution temperature through light‐controlled molecular recognition between the azobenzene moiety on the surface of AuNPs and free α‐CD.
The optimization of photorefractivity (PR) based on a poly(N‐vinylcarbazole) (PVCz) composite devise is proposed from the perspectives of chemistry and physics. The device's PR chemistry (dependence of PVCz's molecular weight) and physics (dependence of grating periodicity and laser wavelength) are studied. Increasing the molecular weight of PVCz from 23 000 to 1 270 000 g mol?1 significantly increases diffraction efficiency, grating build‐up speed (inverse of response time), and sensitivity. Narrowing grating period from 5.1 to 1.1 μm gives faster response time and larger optical gain. Shorter wavelength of writing laser from 633 to 532 nm provides higher diffraction efficiency, faster response time, and larger optical gain.
Novel polyureas are synthesized from lysinyl residues. The polyurea thus prepared yields a durable self‐standing membrane that can be converted into a molecular recognition material by using Z‐D ‐Glu or Z‐L ‐Glu as a print molecule. The Z‐D ‐Glu molecularly imprinted membrane adsorbes the D ‐isomer of Glu in preference to the corresponding L ‐Glu and vice versa. Even though the polyurea consists of L ‐lysinyl residues, both Z‐D ‐Glu and Z‐L ‐Glu work as print molecules to construct molecular (chiral) recognition sites in the membrane. Those molecularly imprinted membranes show chiral separation abilities when a concentration gradient or an applied potential difference is applied as a driving force for membrane transport.
D‐A‐D‐type polymers are of high interest in the field of photovoltaics and electrochromism. In this study we report the synthesis and electrochemical properties of PPyBT along with its photophysical properties and photovoltaic performance. PPyBT is soluble in common organic solvents and both n‐ and p‐type dopable, which is a desired property for conjugated polymers. During electrochemistry studies, the onset potentials of the polymer were determined as +0.2 V for oxidation and ?1.4 V for reduction. Using these values, HOMO and LUMO energy levels were calculated. The photovoltaic properties of PPyBT were also studied. PL studies showed that there is a charge transfer between PPyBT (donor) and PCBM (acceptor).
Summary: The polycondensation of 1‐ethynyl‐2,5‐dihexyl‐4‐iodobenzene in the presence of 1‐ethynyl‐2,5‐dihexyl‐4‐(2‐phenylethynyl)benzene proceeds according to the mechanism of initiated chain growth polycondensation. It has allowed the synthesis of oligomers with a desired molecular weight and a narrow molecular weight distribution. The reasons for the side reaction leading to the formation of diyne compounds are revealed and the presumed mechanism is given. This opens prospects for the preparation of defectless poly(p‐phenyleneethynylene)s with required molecular weights and narrow molecular weight distributions.
Biodegradable and photocurable block copolymers of ε‐caprolactone and L ‐lactide were synthesized by polycondensation of PLLA diol ( = 10 000 g · mol?1), PCL diol ( = 10 000 g · mol?1), and a chain extender bearing a coumarin group. The effect of copolymer composition on the thermal and mechanical properties of the photocured copolymers was studied by means of DSC and cyclic tensile tests. An increase in Young's modulus and a decrease in the tensile strain with increasing PLLA content was observed for the block copolymers. Block copolymers with high PCL content showed good to excellent shape‐memory properties. Random copolymers exhibited Rf and Rr values above 90% at 45 °C for an extremely large tensile strain of 1 000%.
Summary: The successful incorporation of hydroquinone in thermal polyesterifications to prepare rigid linear copolyesters is hindered by the leaving group ability of phenols in nucleophilic acyl substitution reactions, the low nucleophilicity of phenols relative to aliphatic alcohols, and its volatility. To overcome these obstacles, with particular regard to improving the properties of poly(ethylene terephthalate), PET, we chose an approach whereby dyad‐based AB‐type mono(acetoxyphenyl) terephthalate monomers are transesterified into PET. In contrast to attempts to copolymerize terephthalic acid, ethylene glycol (EG) and hydroquinone, the transterification of small amounts (<10 mol‐%) of the preformed dyad in the absence of aliphatic diol, provides homogeneous random copolymers. Incorporation of larger amounts of aromatic diol gave only partly soluble materials. NMR analysis of the soluble fraction (in 20 vol.‐% TFA:CHCl3) indicated that the copolymers are substantially random. Transesterification of mono(4‐acetoxyphenyl) terephthalate (hydroquinone‐terephthalic acid, 1 ) and mono(3‐acetoxyphenyl) terephthalate (resorcinol‐terephthalic acid, 2 ) into PET allows us to further explore the effect of mesogen structure on the development of liquid crystalline copolyesters.
Benzo[1,2‐b:4,5‐b′]diselenophene (BDS) has been incorporated for the first time in a polymer. bis(Stannyl)‐functionalized BDS was copolymerized with 3,3′‐bis(alkyl)‐5,5′‐bithiophenes (dodecyl and tetradecyl side chains) through Stille copolymerization, to yield p‐type polymer semiconductors for organic field‐effect transistor application. The electronic and structural effect of the selenium atoms, compared to sulphur atoms in analogous copolymers, is described. The molecular weight has a decisive influence on the photophysical properties and supramolecular ordering, expressed in field‐effect transistor measurements. Saturation mobilities around 10?2 cm2 · V?1s?1 are obtained on standard silicon substrates.
A new series of disubstituted polyacetylene derivatives that contain multi‐fluorine atoms on the pendent phenyl ring have been synthesized and characterized. The results reveal a greater red‐shift in UV‐vis absorption and PL emission upon incorporating more fluorine atoms on the pendent phenyl ring. Among them, disubstituted polyacetylene with a difluorophenyl group ( PDPA‐2F ) showed the highest luminescent efficiency. The device performance can be promoted by blending a hole‐transporting material TM‐TPD into PDPA‐2F as the active layer or by using a light‐emitting copolymer in which PDPA‐2F was copolymerized with a carbazole group ( PDPA‐2Fcab ). A light‐emitting diode of ITO/PEDOT/ PDPA‐2Fcab /Ca/Al revealed a maximum luminescence of 4230 cd · m?2 at 14 V and a maximum current efficiency of 3.37 cd · A?1 at 7 V.
A general approach to construct one‐dimensional face‐to‐face alignment of porphyrin/fullerene nanowires has been developed. This system uses extended trans‐dihydroxotin(IV) porphyrin and trans‐dicarboxylate‐substituted [60]fullerenoacetic diacid compounds. The nanowires are arranged in regular one‐dimensional linear arrays with lengths in the range 50–300 nm. In the nanowires, each fullerene unit is axially coordinated to the central metal ion of a Sn(IV) porphyrin unit via Sn‐carboxylate coordination and forms a face‐to‐face aligned structure. The synthesis and the hierarchical structure of nanowires have been investigated. They could have potential applications for photoelectronic devices, organic solar cells and so on.
Summary: A cationic polymerization of isobutylene, isobutyl vinyl ether, ethyl vinyl ether, vinylcarbazole and α‐methylstyrene was induced by mixing with poly(vinylidene fluoride) (PVDF) powder. The polymerization was an exothermic reaction and gave a high yield. An electron was abstracted from the monomer by PVDF. By the abstraction of the electron, the monomer was converted to a cation radical which induced polymerization. The generation of the cation radicals of the vinyl ethers was confirmed by an ESR spin trapping method, although the cation radicals could be coupled immediately. The resulting polymer was isolated from PVDF (not grafted) and characterized by size exclusion chromatography, IR, UV‐Vis and NMR spectroscopy. The copolymerization of vinyl ethers or vinyl ether/vinylcarbazole was carried out successfully to obtain their random copolymer. PVDF is regarded as a reusable catalyst for cationic polymerizations.
Reaction mechanism of the cationic polymerization of iBVE. 相似文献
Cross‐linked poly(3,4‐ethylenedioxythiophene) (PEDOT) films were synthesized by the oxidative polymerization of 3,4‐ethylenedioxythiophene in the presence of five different conjugated and non‐conjugated cross‐linkers. The concentration and structure of the cross‐linker was systematically varied to explore the influence on the electrical conductivity. Optimized compositions displayed an electrical conductivity of up to ≈800 S · cm?1; this corresponds to a conductivity increase of up to 36% compared to linear PEDOT prepared under identical conditions. An increase in the conductivity was only observed for the conjugated cross‐linkers that were incorporated in low concentrations, typically at a level of less than 2 mol‐%. Attempts to incorporate higher concentrations of cross‐linker led to phase separation and crystallization of the cross‐linker and afforded materials in which a significant reduction of the electrical conductivity was observed. The optical properties of the polymer were only marginally affected upon cross‐linking, even at high cross‐linker concentrations.
