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Angle-resolved low-energy ion scattering is a valuable technique for examining the topmost surface layers of materials. Using this technique, information about both composition and structure can be obtained. We discuss the physical basis of this technique and present our findings for the fivefold surface of icosahedral (i-) Al–Pd–Mn. Our results clearly show that the exposed surface has a higher Al content than the bulk and can have fivefold periodicity. Information about frequently occurring interatomic distances on the surface can also be obtained by this technique. We discuss the results and compare them to recent scanning tunneling microscopy studies and to bulk structure models. 相似文献
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Photolysis of (R(S),S(C))-1-deuterio-2,2-dimethylpropyl p-tolyl sulfoxide provides mainly (S(S),S(C))-1-deuterio-2,2-dimethylpropyl p-tolyl sulfoxide at low conversion, though the other two stereoisomers are formed to smaller extents. Thus, the predominant process leading to sulfur inversion yields only sulfur inversion, without inversion of the adjacent CHD stereogenic center. This is taken as evidence for a mechanism for photochemical epimerization of sulfoxides that does not involve homolytic alpha-cleavage chemistry. 相似文献
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Gas chromatography/mass spectrometry (GC/MS), with an ion trap mass analyzer, was used to examine the very-long-chain cuticular acid and certain non-acid wax constituents on the leaf sheath surface of Sorghum bicolor before and during 36 hours of light exposure. The mass spectra of the trimethylsilylated acids and alcohols did not match any of those published in searchable mass spectral libraries. The observed differences can be related to the interaction between water and the trimethylsilylated acids and alcohols. Understanding the observed mass spectra of the very-long-chain plant waxes is critical for studies that employ GC/MS with the ion trap mass analyzer to elucidate cuticular wax compositions on plants. 相似文献
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Ina Vollmer Michael J. F. Jenks Mark C. P. Roelands Robin J. White Toon van Harmelen Paul de Wild Gerard P. van der Laan Florian Meirer Jos T. F. Keurentjes Bert M. Weckhuysen 《Angewandte Chemie (International ed. in English)》2020,59(36):15402-15423
Increasing the stream of recycled plastic necessitates an approach beyond the traditional recycling via melting and re‐extrusion. Various chemical recycling processes have great potential to enhance recycling rates. In this Review, a summary of the various chemical recycling routes and assessment via life‐cycle analysis is complemented by an extensive list of processes developed by companies active in chemical recycling. We show that each of the currently available processes is applicable for specific plastic waste streams. Thus, only a combination of different technologies can address the plastic waste problem. Research should focus on more realistic, more contaminated and mixed waste streams, while collection and sorting infrastructure will need to be improved, that is, by stricter regulation. This Review aims to inspire both science and innovation for the production of higher value and quality products from plastic recycling suitable for reuse or valorization to create the necessary economic and environmental push for a circular economy. 相似文献
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Melanie J. Heying Mrinmoy Nag William S. Jenks 《Journal of Physical Organic Chemistry》2008,21(11):915-924
Photolysis of substituted thiophene‐S‐oxides in solution results in the formation of either the corresponding thiophene or furan, in addition to uncharacterized materials. No good rationalization is available for the choice of which pathway may predominate, but it is demonstrated that the photolysis of 2,5‐bistrimethylsilylthiopene‐ S‐oxide produces O(3P) in the same manner as the well‐established photolysis of dibenzothiophene‐S‐oxide. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
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Stoldt CR Caspersen KJ Bartelt MC Jenks CJ Evans JW Thiel PA 《Physical review letters》2000,85(4):800-803
Ag(100) homoepitaxy constitutes one of the simplest systems in which to study thin-film growth. Yet we find that the roughness variation with temperature is extraordinarily complex. Specifically, as the deposition temperature is reduced from 300 to 50 K, the roughness of 25 monolayer films first increases, then decreases, then increases again. A transition from mound formation to self-affine (semifractal) growth occurs at approximately 135 K. The underlying mechanisms are postulated. An atomistic model incorporating these mechanisms reproduces the experimental data quantitatively. 相似文献
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Summary The enantioselectivity of native and derivatized cyclodextrin stationary phases for aromatic and aliphatic chiral sulfoxides
was evaluated using high performance liquid chromatography (HPLC). Many sulfoxide enantiomers could be baseline resolved using
the derivatized cyclodextrin stationary phases in the reverse phase mode. The most important factor influencing enantioselectivity
is the presence of steric bulk alpha to the chiral center. However, substituents on an aromatic ring bonded to the sulfoxide
have less pronounced effects on enantioselectivity. The 2,3-dimethyl β-cyclodextrin exhibits the broadest anantioselectivity
for neutral chiral sulfoxides. Native cyclodextrins and hydroxypropyl-β-cyclodextrins were much less effective in separating
this class of molecules. The hydrogen bonding ability of the organic modifier does not significantly affect enantioselectivity. 相似文献
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A detailed survey of 26 scientific journals showed that journal editors and a majority of authors of the reviewed papers seem unconcerned by the importance of correctly reporting their use of certified reference materials (CRMs). Only around 55% of the abstracts surveyed mention the use of CRMs described in these papers. This, however, is of key importance as the abstract of a paper is most widely available in electronic media. Many authors mentioned the use of CRMs in passing, often in incomplete form and without giving any details of the results obtained. Some are confused about the source of the reference material used, as they fail to report the type or the producer of CRMs applied. Others use materials that do not match the samples analyzed or do not see the need to use any CRM, despite the availability of suitable materials. Even in cases where correct data were given for type and producer of the CRMs, frequently the proper use and statistical evaluation are questionable. To improve this situation it is necessary that publishers should give recommendations where and how the use of CRMs should be described. 相似文献