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101.
Sarah E. Walker Dr. James A. Jordan‐Hore Dr. David G. Johnson Prof. Dr. Stuart A. Macgregor Dr. Ai‐Lan Lee 《Angewandte Chemie (International ed. in English)》2014,53(50):13876-13879
A direct Pd‐catalyzed C? H functionalization of benzoquinone (BQ) can be controlled to give either mono‐ or disubstituted BQ, including the installation of two different groups in a one‐pot procedure. BQ can now be directly functionalized with aryl, heteroaryl, cycloalkyl, and cycloalkene groups and, moreover, the reaction is conducted in environmentally benign water or acetone as solvents. 相似文献
102.
Xiaonan Duan Dr. Stéphane C. Corgié Prof. Daniel J. Aneshansley Prof. Peng Wang Prof. Larry P. Walker Prof. Emmanuel P. Giannelis 《Chemphyschem》2014,15(5):974-980
We report a new family of hierarchical hybrid catalysts comprised of horseradish peroxidase (HRP)–magnetic nanoparticles for advanced oxidation processes and demonstrate their utility in the removal of phenol from water. The immobilized HRP catalyzes the oxidation of phenols in the presence of H2O2, producing free radicals. The phenoxy radicals react with each other in a non‐enzymatic process to form polymers, which can be removed by precipitation with salts or condensation. The hybrid peroxidase catalysts exhibit three times higher activity than free HRP and are able to remove three times more phenol from water compared to free HRP under similar conditions. In addition, the hybrid catalysts reduce substrate inhibition and limit inactivation from reaction products, which are common problems with free or conventionally immobilized enzymes. Reusability is improved when the HRP–magnetic nanoparticle hybrids are supported on micron‐scale magnetic particles, and can be retained with a specially designed magnetically driven reactor. The performance of the hybrid catalysts makes them attractive for several industrial and environmental applications and their development might pave the way for practical applications by eliminating most of the limitations that have prevented the use of free or conventionally immobilized enzymes. 相似文献
103.
Harry J. Whitlow Margaretha Andersson Mikael Hult Leif Persson Mohamed El Bouanani Mikael Östling Carina Zaring Nils Lundberg David D. Cohen Nick Dytlewski Peter N. Johnston Ian F. Bubb Scott R. Walker Erik Johanson Sture Hogmark P. Anders Ingemarsson 《Mikrochimica acta》1995,120(1-4):171-181
Recoil Spectrometry covers a group of techniques that are very similar to the well known Rutherford backscattering Spectrometry technique, but with the important difference that one measures the recoiling target atom rather than the projectile ion. This makes it possible to determine both the identity of the recoil and its depth of origin from its energy and velocity, using a suitable detector system. The incident ion is typically high-energy (30–100MeV)35C1,81Br or127I. Low concentrations of light elements such as C, O and N can be profiled in a heavy matrix such as Fe or GaAs. Here we present an overview of mass and energy dispersive recoil Spectrometry and illustrate its successful use in some typical applications. 相似文献
104.
D. Greig M. J. Hall C. Hammond B. J. Hickey H. P. Ho M. A. Howson M. J. Walker N. Wiser D. G. Wright 《Journal of magnetism and magnetic materials》1992,110(3):L239-L246
We report the first observation of a giant magnetoresistance (MR) in Co/Cu superlattices grown by MBE. The maximum value of the MR is - 26% and this is found in a specimen for which the copper layers are about 7 Å thick and which includes a thin 10 Å layer of gold in the buffer region between the substrate and the superlattice. From RHEED and X-ray diffraction it is shown that the metallic layers in the specimens grown in this way are extremely flat and that the orientation of the copper is (111). 相似文献
105.
106.
107.
Bennett N. Walker Jessica A. Stolee Deanna L. Pickel Scott T. Retterer Akos Vertes 《Applied Physics A: Materials Science & Processing》2010,101(3):539-544
Experimental assessment of the thermal load induced by fast laser pulses on micro- and nanostructures through IR imaging is
currently too slow and lacks the spatial resolution to be useful. In this paper, we introduce a method based on measuring
the laser-induced yields of ions to compare the thermal loads on nanofabricated silicon structures, when exposed to nanosecond
laser pulses. The laser fluences at which the ion yields of, for example, sodiated and potassiated peptides ions are equal
for two different structures correspond to equivalent thermal loads. Using alkalinated peptides is a convenient choice because
the corresponding ion intensities are easily measured up to the melting point of silicon. As an example, we compare the nanosecond
laser heating of silicon nanopost arrays with diverse post diameters and periodicities. Assessment of the thermal load through
ion yield measurements can also be used to verify model assumptions for heat transport regimes in nanostructures. 相似文献
108.
109.
Under sections 73 and 74 of the revised Canadian Environmental Protection Act (CEPA 1999), Environment Canada and Health Canada must "categorize" and "screen" about 23,000 substances on the Domestic Substances List (DSL) for persistence (P), bioaccumulation (B), and inherently toxic (iT) properties. Since experimental data for P, B and iT are only available for a few DSL substances, a workshop was held to address issues associated with the use of Quantitative Structure-Activity Relationships (QSARs) to categorize these substances. This paper describes the results of an 11-12 November 1999 International Workshop sponsored by Environment Canada to discuss potential uses and limitations of QSARs to categorize DSL substances as either persistent or bioaccumulative and iT to non-human organisms and to recommend future research needed to develop methods for predicting the P, B and iT of difficult-to-model substances. 相似文献
110.
A pulsed jet cavity Fourier transform microwave spectrometer has been used to measure the rotational spectra of OCAgX (X = F, Cl, Br) in the frequency range 5-22 GHz. Metal atoms were generated via laser ablation and were allowed to react with CO and a halide precursor, prior to stabilization of the products within a supersonic jet of argon. These are the first experimental observations of OCAgF and OCAgBr, and the first high resolution spectroscopic study of OCAgCl. All three molecules are linear. Accurately determined rotational constants have been used to evaluate the various internuclear distances, which are found to be consistent with trends established for OCAuX and OCCuX species. The C-O distances are short, and the M-C distances are significantly longer than those in other molecules containing a metal-carbonyl bond. Precise values of centrifugal distortion constants and halogen nuclear quadrupole coupling constants have also been determined. The coupling constants are compared with the results of previous studies of OCCuX and OCAuX and are used to infer trends in the electron distributions of the molecules. Ab initio calculations have been performed and employed to predict the geometries, vibrational frequencies, and Mulliken valence orbital populations of the various species. 相似文献