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Cross-coupling reactions, such as Buchwald-Hartwig arylamination and direct intramolecular biaryl coupling by C–H activation, were carried out using various Palladium-N-heterocyclic carbenes (Pd–NHC) as catalysts. The yields were good to excellent. The latter strategy was adopted to transform two dibenzylbutane lignans, isolated from the leaves of Ocotea macrophylla (Lauraceae), into the corresponding dibenzocyclooctane lignans in good overall yields. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications® to view the free supplemental file. 相似文献
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Coy L. May 《代数通讯》2013,41(11):4078-4095
Let G be a finite group. The symmetric genus σ (G) is the minimum genus of any compact Riemann surface on which G acts faithfully as a group of automorphisms. Here we classify the groups of symmetric genus σ, for all values of σ such that 4 ≤ σ ≤ 8. In addition, we obtain some general results about the partial presentations that groups acting on surfaces must have. We show that a group with even genus and no “large order” elements in its Sylow 2-subgroup has restrictions on its Sylow 2-subgroup. As a consequence, we show that if G is a 2-group with positive symmetric genus, then σ(G) is odd. The software package MAGMA was employed to help with the calculations, and the MAGMA library of small groups was essential to the classification. 相似文献
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M.W. Todd R.A. Provencal T.G. Owano B.A. Paldus A. Kachanov K.L. Vodopyanov M. Hunter S.L. Coy J.I. Steinfeld J.T. Arnold 《Applied physics. B, Lasers and optics》2002,75(2-3):367-376
A novel instrument, based on cavity-ringdown spectroscopy (CRDS), has been developed for trace gas detection. The new instrument
utilizes a widely tunable optical parametric oscillator (OPO), which incorporates a zinc–germanium–phosphide (ZGP) crystal
that is pumped at 2.8 μm by a 25-Hz Er,Cr:YSGG laser. The resultant mid-IR beam profile is nearly Gaussian, with energies
exceeding 200 μJ/pulse between 6 and 8 μm, corresponding to a quantum conversion efficiency of approximately 35%. Vapor-phase
mid-infrared spectra of common explosives (TNT, TATP, RDX, PETN and Tetryl) were acquired using the CRDS technique. Parts-per-billion
concentration levels were readily detected with no sample preconcentration. A collection/flash-heating sequence was implemented
in order to enhance detection limits for ambient air sampling. Detection limits as low as 75 ppt for TNT are expected, with
similar concentration levels for the other explosives.
Received: 1 April 2002 / Revised version: 13 June 2002 / Published online: 12 September 2002
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ID="*"Corresponding author. Fax: +1-408/524-0551, E-mail: mtodd@picarro.com 相似文献
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S. Feliu Jr M. C. Merino R. Arrabal A. E. Coy E. Matykina 《Surface and interface analysis : SIA》2009,41(3):143-150
The surface characteristics and corrosion behaviour of the AZ31 magnesium alloy exposed to a high relative humidity (RH) atmosphere were investigated. During the first 15 days of humidity test at 98% RH and 50 °C, a significant increase of magnesium carbonate and a decrease of magnesium oxide were detected on the surface film by XPS; after this stage, increased exposure times did not produce substantial changes on the relative amounts of these compounds. The surface film of commercially pure magnesium, also examined for comparison purposes, revealed more magnesium carbonate and less magnesium oxide compared with the AZ31 alloy. Unlike the AZ31 alloy, the surface of pure Mg disclosed almost complete substitution of MgO by magnesium carbonate after 30 days of exposure time. Mass gain values of tested specimens and scanning electron microscope characterisation of corroded surfaces indicated lower corrosion susceptibility of the AZ31 alloy compared with the commercially pure Mg, suggesting superior chemical stability of the oxide/hydroxide film formed over the magnesium–aluminium alloy surface. XPS and energy dispersive X‐ray (EDX) analyses did not revealed any substantial enrichment of aluminium in the corrosion products film on the AZ31 alloy after 30 days of testing. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
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Ericsson D. Coy‐Barrera Luis E. Cuca‐Surez Michael Sefkow Uwe Schilde 《Acta Crystallographica. Section C, Structural Chemistry》2012,68(8):o320-o322
The structure of naturally‐occurring cinerin C [systematic name: (7S,8R,3′R,4′S,5′R)‐Δ8′‐4′‐hydroxy‐5,5′,3′‐trimethoxy‐3,4‐methylenedioxy‐2′,3′,4′,5′‐tetrahydro‐2′‐oxo‐7.3′,8.5′‐neolignan], isolated from the ethanol extract of leaves of Pleurothyrium cinereum (Lauraceae), has previously been established by NMR and HRMS spectroscopy, and its absolute configuration established by circular dichroism measurements. For the first time, its crystal strucure has now been established by single‐crystal X‐ray analysis, as the monohydrate, C22H26O7·H2O. The bicyclooctane moiety comprises fused cyclopentane and cyclohexenone rings which are almost coplanar. An intermolecular O—H...O hydrogen bond links the 4′‐OH and 5′‐OCH3 groups along the c axis. 相似文献
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W. Prandtl A. Brukl L. Pauling H. N. Mc Coy Ida Noddack J. K. Marsh L. Holleck W. Noddack G. Urbain F. Bourion G. Jantsch H. Albers H. Grubitsch P. W. Selwood J. A. C. Bowles H. M. Partridge H. C. Fogg L. Hess H. H. Williard N. K. Tang E. A. Werner C. James H. C. Holden A. J. Grant J. P. Bonardi Leonid Kuhlberg F. M. Semiakin 《Analytical and bioanalytical chemistry》1938,113(3-4):121-135