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401.
402.
The development of efficient methods for stereocontrolled synthesis of polyol derivatives has been of continuing interest for the synthetic community. We describe herein tandem olefin cross‐metathesis/hemiacetalization/intramolecular oxa‐Michael addition of allylic/homoallylic alcohols, α,β‐unsaturated ketones, and aldehydes, which enabled the synthesis of syn‐1,2‐ and syn‐1,3‐diol derivatives in a step‐economical manner. A series of differentially protected polyol derivatives could be obtained in subsequent transformations via chemoselective/regioselective cleavage of the acetal moiety of the tandem reaction products.  相似文献   
403.
404.
Inorganic chemical cells (iCHELLs) are compartment structures consisting of polyoxometalates (POMs) and cations, offering structured and confined reaction spaces bounded by membranes. We have constructed a system capable of efficient anisotropic and hierarchical photo‐induced electron transfer across the iCHELL membrane. Mimicking photosynthesis, our system uses proton gradients between the compartment and the bulk to drive efficient conversion of light into chemical energy, producing hydrogen upon irradiation. This illustrates the power of the iCHELL approach for catalysis, where the structure, compartmentalisation and variation in possible components could be utilised to approach a wide range of reactions.  相似文献   
405.
In a class of supersymmetric flavor models predictions are based on residual symmetries of some subsectors of the theory such as those of the charged leptons and neutrinos. However, the vacuum expectation values of the so-called flavon fields generally modify the Kähler potential of the setting, thus changing the predictions. We derive simple analytic formulae that allow us to understand the impact of these corrections on the predictions for the masses and mixing parameters. Furthermore, we discuss the effects on the vacuum alignment and on flavor changing neutral currents. Our results can also be applied to non-supersymmetric flavor models.  相似文献   
406.
Isotopic signatures of atmospheric methanol and acetaldehyde have the potential to improve our ability to quantitatively assess their importance in atmospheric chemistry. However, isotopic measurements of atmospheric methanol and acetaldehyde and their individual source and sink processes have been limited. In this study, we examined gas chromatography-isotope ratio mass spectrometry combined with headspace solid-phase microextraction to measure the carbon isotope ratios of methanol and acetaldehyde in air samples. The method enabled us to determine carbon isotope ratios with a precision (1 standard deviation) of±0.6 ‰ for 20 ml of air sample containing more than 3 ppm of methanol and±0.7 ‰ for 20 ml of air sample containing more than 2 ppm of acetaldehyde. Moreover, the applicability of this method to determine isotope ratios of methanol and acetaldehyde emitted from detached plant leaves was demonstrated.  相似文献   
407.
408.
The step-terrace structures at the interface between the Si layer and the buried SiO2 layer of a Separation by IMplanted OXygen substrate has been observed by using atomic force microscopy (AFM) after removing the SiO2 and Si layers. The time evolution of the Si–SiO2 interface roughness during high-temperature annealing was analyzed by the scaling analysis of AFM data. The correlation length exhibited a nice correspondence to the size of square domain structures. Decreasing in the index of the length scale indicates that the growth mechanism changes as the annealing proceeds.  相似文献   
409.
The pump performance of a small air-lift system in transporting solid particles is investigated experimentally. Three types of riser pipe were used to examine the effect of local bends of riser pipes on the flow characteristics of a three-phase air–water–solid particles mixture. Two of them were locally S-shaped either below or above a gas injector. The other was vertically straight. Alumina particles of 3 or 5 mm diameter were used as solid particles. It is indicated that the pump performance is appreciably reduced when the pipe bend is above the gas injector. The critical condition under which solid particles are vertically lifted is discussed from a practical viewpoint. In addition, the particle motion in the region of a pipe bend is investigated by photographic observations.  相似文献   
410.
We first prepared polymer‐bound photoluminescent iridium complexes bearing a cyclometalated 2,2′‐biphenylene ligand via an easy procedure in which the metallopolymer was synthesized by the reaction of a metal precursor with a polymer ligand. The iridium compound, [Ir(cod)(biph)Cl]2 (where cod and biph are 1,5‐cyclooctadiene and biphenyl‐2,2′‐diyl, respectively), was used as the iridium material, and a copolymer built by the radical copolymerization of 4‐styryldiphenylphosphine and methyl methacrylate was employed as the polymer ligand. The obtained metallopolymers were highly crosslinked by iridium atoms forming P? Ir? P bonds. The content of the iridium was experimentally clarified to be in the range of 0.06–0.6 mmol/g of the polymer. Photoluminescence of the iridium polymer in the solid state was observed at 597 nm when the polymer was irradiated at 350 nm. As the Ir content in the copolymer increased to 0.2 mmol/g, the intensity of the luminescence also increased, but more iridium content decreased the intensity. Furthermore, the intensity of the photoluminescence in these photoluminescent polymers depended on the molecular weight of the copolymer ligands. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4204–4213, 2006  相似文献   
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