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Niels ten Brummelhuis Marcus Weck 《Journal of polymer science. Part A, Polymer chemistry》2014,52(11):1555-1559
Reversible addition‐fragmentation chain‐transfer (RAFT) polymerization was used to control the alternating copolymerization of styrene and 2,3,4,5,6‐pentaflurostyrene. The RAFT polymerization yields a high degree of control over the molecular weight of the polymers and does not significantly influence the reactivity ratios of the monomers. The controlled free‐radical polymerization could be initiated using AIBN at elevated temperatures or using a redox couple (benzoyl peroxide/N,N‐dimethylaniline) at room temperature, while maintaining control over molecular weight and dispersity. The influence of temperature and solvent on the molecular weight distribution and reactivity ratios were investigated. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1555–1559 相似文献
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Michèle Fee Spyridon Ntais Arnaud Weck Elena A. Baranova 《Journal of Solid State Electrochemistry》2014,18(8):2267-2277
Thin silver films (100–800 nm) were deposited by physical vapor deposition (PVD) on yttria-stabilized zirconia solid electrolyte. The electric percolation as a function of the film thickness was studied during deposition and annealing using a two-electrode in-situ resistance measurement technique. Electrical percolation was achieved in as-deposited films greater than 5.4?±?0.4 nm; however, thermal treatment (550 °C in air) resulted in film dewetting for Ag films as thick as 500 nm and formation of electronically isolated Ag nanoparticles, as was confirmed by SEM and XPS. In thermally treated samples, stable electronic conductivity associated with a continuous percolated network was only observed in samples greater than 600 nm in thickness. The effect of polarization on the electrochemical reactions at the three-phase (electrode-gas-electrolyte) and two-phase (electrode-electrolyte) boundaries of the electrode was investigated by solid electrolyte cyclic voltammetry (SECV) at 350 °C and P O2?=?6 kPa. With the application of positive potential, silver oxide (Ag2O) was found to form along the three-phase boundary and then extends within the bulk of the electrode with increasing anodic potentials. By changing the hold time at positive potential, passivating oxide layers are formed which results in a shift in favor of the oxygen evolution reaction at the working electrode. This oxide forms according to a logarithmic rate expression with thick oxides being associated with decrease in current efficiency for subsequent oxide formation. 相似文献
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Michele Arcangelo Quinto Juan Manuel Monti Mario Enrique Alcocer Avila Philippe F. Weck Omar Ariel Fojón Roberto Daniel Rivarola Christophe Champion 《X射线光谱测定》2020,49(1):95-98
The present work focuses on studying the contribution of the Auger electron emission in proton-induced interactions in biological matter. The Monte Carlo track-structure code, TILDA-V, was then used for modeling the protons beams of 10 keV to 100 MeV in biological matter, namely, water vapor and hydrated DNA. The main ionizing processes are described by means of an extensive set of ab initio differential and total cross sections computed within a quantum-mechanical CDW-EIS approximation. 相似文献
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Xiaolong Zheng Mingzhu Liu Mingxin He Prof. David J. Pine Prof. Marcus Weck 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(20):5599-5603
A facile method to synthesize shape-shifting patchy particles on the colloidal scale is described. The design is based on the solvent-induced shifting of the patch shape between concave and convex features. The initial concave patchy particles were synthesized in a water suspension by a swelling-induced buckling process. Upon exposure to different solvents, the patches were tuned reversibly to be either concave or convex. These particles can be assembled into chained, branched, zigzag, and cyclic colloidal superstructures in a highly site-specific manner by surface–liquid capillary bridging. The biphasic nature of the particles also enables site-selective surface functionalization. 相似文献
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Poineau F Malliakas CD Weck PF Scott BL Johnstone EV Forster PM Kim E Kanatzidis MG Czerwinski KR Sattelberger AP 《Journal of the American Chemical Society》2011,133(23):8814-8817
Technetium dichloride has been discovered. It was synthesized from the elements and characterized by several physical techniques, including single crystal X-ray diffraction. In the solid state, technetium dichloride exhibits a new structure type consisting of infinite chains of face sharing [Tc(2)Cl(8)] rectangular prisms that are packed in a commensurate supercell. The metal-metal separation in the prisms is 2.127(2) ?, a distance consistent with the presence of a Tc≡Tc triple bond that is also supported by electronic structure calculations. 相似文献
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Weck PF Gong CM Kim E Thuéry P Czerwinski KR 《Dalton transactions (Cambridge, England : 2003)》2011,40(22):6007-6011
The structure of the uranyl-diacetohydroxamate compound, UO(2)(C(2)NO(2)H(4))(2), was elucidated using a combination of single crystal X-ray diffraction measurements and all-electron scalar relativistic density functional calculations. This polymeric compound crystallizes in the C2/c space group (IT No. 15; a = 12.8386(13) ?, b = 7.5661(7) ?, c = 8.9299(9) ?, β = 103.185(2) °; Z = 4), with main-chain repeating units featuring a bidentate structure analogous to that frequently found for d-block as well as lanthanide metal ions. Density functional analysis reveals that this compound is a semiconductor, with a direct band gap of 1.1 eV. 相似文献
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We report first-principles calculations of the structures and properties of technetium nitride phases within the framework of gradient-corrected density functional theory. Specifically, we have investigated the possible existence of hexagonal Tc(3)N and Tc(2)N subnitrides, following the recent discovery of Re nitrides analogues synthesized directly from the elements. These novel Tc subnitride phases, which are predicted to be stable, are also compared with bulk Tc and Tc mononitride in order to shed light on the intrinsic relationships between the structure, Tc/N stoichiometry, and properties in the Tc-N system. 相似文献