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Molecularly imprinted hydrogel layer SPR sensor chips with lectin-recognition sites, which were prepared via surface-initiated atom transfer radical polymerization (SI-ATRP) combined with molecular imprinting, exhibited not only large SPR signal change in response to a target lectin but also inhibited nonspecific protein adsorption.
The effects of long-term storage of poly(3-hydroxbutyrate-co-3-hydroxyvalerate) were evaluated over a range of temperatures. As the storage temperatures were increased towards 100 °C, secondary crystallisation resulted increasing the melting point, Tg, modulus and strength. At 125 and 150 °C secondary crystallisation and degradation occurred simultaneously; the effects of degradation masked by secondary crystallisation. The significant observation is that the degradation process remains active at storage temperatures well below the melting point and long-term stability of P(3HB-co-3HV) is not only affected by secondary crystallisation, but also sub-melting point degradation.
The alternating conjugated polymer was synthesized with thiophene-substituted aza-boron dipyrromethene. The synthesized polymer had the near-infrared light-absorbing ability (molar extinct coefficient: 48,000 M−1cm−1) in the region over 1300 nm with the peak at 864 nm. From the electrochemical data, it was found that the polymer had the deep lowest unoccupied molecular orbital (LUMO) level. This result means that only the highest occupied molecular orbital level was influenced and the LUMO can be preserved by extension of π-conjugation through the polymer main-chain.
An immiscible blend of isotactic polypropylene (PP) and ethylene-butene-1 copolymer (EB) containing a small amount of N,N'-dicyclohexyl-2,6-naphthalene dicarboxamide as a nucleating agent to generate β-form crystals was prepared by T-die extrusion. We successfully prepared an extruded sheet in which the orientation of the PP molecules is perpendicular to the deformation of the EB particles. It is suggested that EB barely affects the crystalline form and orientation of PP. Since this sheet containing a large amount of β-form crystals exhibits an extraordinary structure, unique mechanical anisotropy is obtained.
To synthesize CO2-derived polycarbonates with high Tg values, epoxides having rigid and bulky 2-norbornyl or 1-adamantyl substituents were selected as comonomers. The alternating copolymer obtained from 1-adamantylethylene oxide showed a Tg above 150 °C. This is the highest Tg among those observed for alternating copolymers obtained from CO2 and a terminal epoxide.
An efficient method to decrease dielectric constant (ɛ) of poly(2,6-dihydroxy-1,5-naphthylene) (PDHN) by introducing bulky alkyl side chains was reported. Poly(2,6-dialkoxy-1,5-naphthylene)s (PDANs) were prepared by the O-alkylation of PDHN with alkyl halides. The ɛ values of PDANs at 10 GHz decreased as the length and size of side chains increased. Especially, PDCHMN exhibited the lowest dielectric constant (ɛ = 2.29). The ε value results were also supported by refractive index measurement.
By simply coating a thin layer of 4,4’-diphenylmethane diisocyanate, polyacrylic acid and borax on the surface of PET film, a transparent PET film with extremely low gas vapor barrier value can be obtained. The oxygen transmission rate can be dramatically decreased to the detection limit of commercial instrumentation (<0.005 cc/m2/day).
Synthesis and properties of borafluorene-containing conjugated polymers with various comonomers are presented. From the comparison with the gallafluorene copolymers, higher luminescent quantum yields were obtained from the borafluorene copolymers. Additionally, from the electrochemical measurements, it was shown that the electron-withdrawing property of the boron atoms led to the stabilization of LUMOs of the borafluorene copolymers. In the X-ray diffraction profiles, the significant peaks originated from π−π stacking and assembly of the side chains were observed. The borafluorene copolymers were more crystalline materials relative to the gallafluorene polymers.
The thermoresponsive copolymer P(MEO2MA-co-OEGMA500) was successfully prepared using a novel photopolymerization procedure. The synthesis was carried out using a user-friendly method with a few ppm of a photoredox iridium-based catalyst. Monomer conversions higher than 50% were achieved in less than 1 h of synthesis showing a faster polymerization rate when compared to the traditional Cu-based ATRP synthesis. The photochemically controlled method here described provides true control over polymer structure, architecture, and properties. Furthermore, the polymer showed no toxicity on four mammalian cell lines at the highest concentration tested (0.4 mg/ml).