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161.
We study the nonlinear rheological behavior and the microscopic particle dynamics for a colloidal glass, to see whether recently developed models for driven glassy systems can be applied to predict the rheology. Qualitatively, all the findings predicted by the models can be retrieved in our system. Notably, the viscosity decreases strongly with the shear rate. Since it is difficult to predict non-Newtonian viscosities of colloidal systems due to long-ranged hydrodynamic interactions, this shows the promise of this approach for predicting flow behavior. In addition, the measurements allow us to relate the microscopic diffusion dynamics to the macroscopic viscosity of the system.  相似文献   
162.
We study the thickness of wetting layers in the binary-liquid mixture cyclohexane methanol. Far from the bulk critical point, the wetting layer thickness is independent of temperature, resulting from the competition between van der Waals and gravitational forces. Upon approaching the bulk critical temperature [t=(T(c)-T)/T(c)-->0], we observe that the wetting layer thickness diverges as t(-beta) with effective critical exponent beta=0.23+/-0.06. This is characteristic of a broad, intermediate scaling regime for the crossover from van der Waals wetting to critical scaling. We predict beta=beta/3 approximately 0.11, with beta the usual bulk-order parameter critical exponent, showing a small but significant difference with experiment.  相似文献   
163.
The reactivity of 1,2,4-trioxane molecules 2-5, structurally related to the antimalarial drug artemisinin, with a heme model, manganese(II) tetraphenylporphyrin, is reported. With the pharmacologically active drugs 2-4, covalent adducts were obtained by addition of a drug-derived radical onto the porphyrin macrocycle, whereas no reaction was obtained with the nonactive compound 5. This confirms that alkylation is probably one of the key factors of the pharmacological activity of endoperoxide-based antimalarial drugs.  相似文献   
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Direct synthesis of luminescent SiC quantum dots in pure deionized water by laser ablation is reported. A zeta‐potential of –49 mV, higher than for nanoparticles produced by electrochemical etching, suggests a higher colloidal stability of the laser‐produced nanoparticles. IR spectroscopy shows that surface charges related to carboxylate anions ensure long‐term stability of the colloidal solutions based on the as‐prepared SiC quantum dots. Main radiative channel at room temperature corresponds to the recombination of quantumly confined photogenerated charge carriers. Emission from the nanoparticles is mainly centred at 2.75 eV regardless of laser power used for ablation. According to photoluminescence spectra, a partial transformation of the SiC quantum dots from cubic to hexagonal crystalline arrangement is supposed. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
169.
The additivity of nonsimultaneous masking was studied using Gaussian-shaped tone pulses (referred to as Gaussians) as masker and target stimuli. Combinations of up to four temporally separated Gaussian maskers with an equivalent rectangular bandwidth of 600 Hz and an equivalent rectangular duration of 1.7 ms were tested. Each masker was level-adjusted to produce approximately 8 dB of masking. Excess masking (exceeding linear additivity) was generally stronger than reported in the literature for longer maskers and comparable target levels. A model incorporating a compressive input/output function, followed by a linear summation stage, underestimated excess masking when using an input/output function derived from literature data for longer maskers and comparable target levels. The data could be predicted with a more compressive input/output function. Stronger compression may be explained by assuming that the Gaussian stimuli were too short to evoke the medial olivocochlear reflex (MOCR), whereas for longer maskers tested previously the MOCR caused reduced compression. Overall, the interpretation of the data suggests strong basilar membrane compression for very short stimuli.  相似文献   
170.
A mixed‐valence {MnII3MnIIIFeII2FeIII2} cyanide‐bridged molecular cube hosting a caesium cation, Cs?{Mn4Fe4}, was synthesized and structurally characterized by X‐ray diffraction. Cyclic‐voltammetry measurements show that its electronic state can be switched between five different redox states, which results in a remarkable electrochromic effect. Magnetic measurements on fresh samples point to the occurrence of a spin‐state change near room temperature, which could be ascribed to a metal‐to‐metal electron transfer converting the {FeII?CN?MnIII} pair into a {FeIII?CN?MnII} pair. This feature was only previously observed in the polymeric MnFe Prussian‐blue analogues (PBAs). Moreover, this novel switchable molecule proved to be soluble and stable in organic solvents, paving the way for its integration into advanced materials.  相似文献   
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