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ABSTRACT The first use of a new mechanosynthesized copper complex (Cu(acac)(2dppba)) as a initiator for the redox and redox photoactivated polymerization of methacrylates under air is proposed. This paper (i) describes the mechanosynthesis of this complex, (ii) outlines the relative efficiency of the complex for redox polymerization (mechanosynthesized product vs. solvent synthesized product), (iii) follows the polymerization enhancement under a 405 nm light, and (iv) demonstrates the high performance of this complex in near infrared photoactivated redox polymerization where a completely colorless polymer is obtained (unprecedented under NIR irradiations, 785 nm, here). The light activated polymerization exhibit higher conversions, better time controls (activation control) and higher surface conversions than redox polymerization. The mechanosynthesis is well characterized by two solvent-free methods (visual color change and Electron Spin Resonance) and two solvent-based methods (high resolution-electrospray ionization-mass spectrometry (HR-ESI-MS) and UV-vis spectrometry). The involved mechanisms are discussed. Mechanosynthesis of copper complexes opens new perspectives for copper (photo)redox polymerization catalysts as the environmental impact and economical costs of the complex synthesis are significantly reduced. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 3646-3655 [ABSTRACT FROM AUTHOR]

This investigation presents the use of a photoredox catalyst "G1" as a photoinitiating system for free radical/cationic hybrid polymerization under mild irradiation conditions. The G1 system (G1/iodonium salt/ N -vinylcarbazole), can simultaneously initiate the free radical and cationic polymerization reactions upon exposure to a visible (405 nm) light from a Light Emitting Diode (LED) source. The multicomponent G1 system is able to simultaneously generate radical and cationic species through a catalytic photoredox process. The curing of thin samples (25 μm), thick samples (1.4 mm) as well as the manufacture of hybrid system/glass fibers composites (˜2 to 4 mm thickness) was realized and the influence of the ratio of cationic/radical monomer blends on the polymerization kinetics was studied. The use of G1 in visible light photoinitiating system for the access to composites and 3D printing experiments was particularly outlined. G1 was also shown to have low levels of migration from the cured materials. When compared to reference materials ("F1", a similar copper complex and an anthracene derivative, dibutoxy anthracene), G1 showed better polymerization efficiency. The initiation efficiency was investigated through the real-time Fourier transform infrared (RT-FTIR) spectroscopy and optical pyrometry. Dynamical Mechanical Analysis has been used to determine the glass temperature transition of the cured hybrid system as a complementary technique. [ABSTRACT FROM AUTHOR]

Aconitum karacolicum from northern Kyrgyzstan (Alatau area) contains about 0.8–1% aconitine as well as other aconite derivatives that have already been identified. In this paper, we compare several methods for the further purification of an Aconitum karacolicum extract initially containing 80% of aconitine. Reverse-phase flash chromatography, reverse-phase semi-preparative HPLC, centrifugal partition chromatography (CPC) and recrystallization techniques were evaluated regarding first their efficiency to get the highest purity of aconitine (over 96%) and secondly their applicability in a semi-industrial scale purification process (in our case, 150 g of plant extract). Even if the CPC technique shows the highest purification yield (63%), the recrystallization remains the method of choice to purify a large amount of aconitine as i) it can be easily carried out in safe conditions; ii) an aprotic solvent is used, avoiding aconitine degradation. Moreover, this study led us to the identification of lappaconitine in Aconitum karacolicum , a well-known alkaloid never found in this Aconitum species. [ABSTRACT FROM AUTHOR]

Abstract: Light-emitting electrochemical cells (LECs) based on a semiconducting polymer blended with lithium salt and novel polyelectrolytes have been studied. Random copolymers of poly(ethylene glycol) methyl ether methacrylate have been developed in order to increase their glass transition temperature (T g) above room temperature. Devices have been optimized and successfully turned on upon heating. Cooling devices under applied voltage bias down to room temperature leads to frozen PN junctions. The relaxation of these junctions over voltage-free storage is studied. The higher the T g, the longer the shelf-life of the junctions. This research opens the route to room temperature stable organic PN junctions for use in organic electronic devices such as light-emitting diodes, photovoltaic solar cells and other organic electronic devices. [Copyright &y& Elsevier]

Rectifying antennas are often prensented as a potentiel technological breakthrough for energy harvesting. First theorized in the 1970's, the downsizing of an antenna coupled with a rectifier has become technologically achievable with the progresses of fabrication techniques such as electron beam or photolithography. However, reaching infrared or visible region of the electromagnetic spectra still entails challenges on the integration of a rectifier operating in the terahertz range. New bottom up approaches are likely to bring a promising solution to this issue. To improve our understanding of the key points of rectifying antennas' design for the infrared and visible light, and the challenges of device fabrication, this work reviews the progresses of this technology, going back from the first historical RF energy harvesting systems and covering the most innovative trends to this date. [ABSTRACT FROM AUTHOR]