排序方式: 共有39条查询结果,搜索用时 27 毫秒
1.
2.
3.
Bharat Kumar Ruth L. Viboh Margel C. Bonifacio William B. Thompson Jonathan C. Buttrick Babe C. Westlake Min‐Soo Kim Robert W. Zoellner Sergey A. Varganov Philipp Mrschel Jaroslav Teteruk Martin U. Schmidt Benjamin T. King 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2012,124(51):13071-13071
4.
R.L. Rasera G.K. Shenoy B.D. Dunlap D.G. Westlake 《Journal of Physics and Chemistry of Solids》1979,40(1):75-77
Time-differential perturbed γ-ray angular correlation experiments have been carried out on 181Ta impurities in ?-phase zirconium hydride over the temperature range from 20 to 588 K. A static, slightly asymmetric electric quadripole interaction is found at all temperatures. The static nature of the pattern indicates the absence of significant hydrogen diffusion at these temperatures on the time scale of the experiment (0.1 μsec). The temperature dependence of the static quadrupole frequency is given by the relation vq(t) = 130[1 ? (1.9 × 10?5)T1.5] MHz. 相似文献
5.
Sundberg TB Darricarrere N Cirone P Li X McDonald L Mei X Westlake CJ Slusarski DC Beynon RJ Crews CM 《Chemistry & biology》2011,18(10):1300-1311
Identification of methionine aminopeptidase-2 (MetAP-2) as the molecular target of the antiangiogenic compound TNP-470 has sparked interest in N-terminal Met excision's (NME) role in endothelial cell biology. In this regard, we recently demonstrated that MetAP-2 inhibition suppresses Wnt planar cell polarity (PCP) signaling and that endothelial cells depend on this pathway for normal function. Despite this advance, the substrate(s) whose activity is altered upon MetAP-2 inhibition, resulting in loss of Wnt PCP signaling, is not known. Here we identify the small G protein Rab37 as a MetAP-2-specific substrate that accumulates in the presence of TNP-470. A functional role for aberrant Rab37 accumulation in TNP-470's mode of action is demonstrated using a Rab37 point mutant that is resistant to NME, because expression of this mutant phenocopies the effects of MetAP-2 inhibition on Wnt PCP signaling-dependent processes. 相似文献
6.
Richard L. Carlin Robert D. Chirico Kyong O. Joung G.K. Shenoy D.G. Westlake 《Physics letters. A》1980,75(5):413-414
In contrast to a previous report, GdH3 is found to order antiferromagnetically at 1.8 K. 相似文献
7.
Westlake P Siozos P Philippidis A Apostolaki C Derham B Terlixi A Perdikatsis V Jones R Anglos D 《Analytical and bioanalytical chemistry》2012,402(4):1413-1432
Wall paintings spanning two millennia of Cretan painting history and technology were analysed in an effort to determine similarities
and evolutions of painting materials and technology. A multi-technique approach was employed that combined the use of (a)
laser-induced breakdown spectroscopy (LIBS) and Raman microspectroscopy, based on mobile instrumentation, appropriate for
rapid, routine-level object characterization, and (b) non-destructive X-ray diffractometry (XRD), performed directly on the
wall painting fragment, which provides detailed information on the minerals constituting the paint. Elemental analysis data
obtained through LIBS were compared with molecular and crystal structure information from Raman spectroscopy and XRD. Cross-sections
from selected samples were also investigated by means of optical microscopy and scanning electron microscopy coupled to micro-probe
analysis and X-ray mapping that enabled identification of several mineral components of the paint confirming the results of
the XRD analysis. In parallel, replica wall paintings, created with known pigments and binding media for reference purposes,
were examined with optical microscopy and stain tested for organic materials. The overall study shows that the LIBS and Raman
techniques offer key advantages, such as instrument mobility and speed of data collection and interpretation that are particularly
important when dealing with on-site investigations. Thus, they are capable of providing important compositional information
in an effective manner that enables quick surveying of wall paintings and permit targeted sample selection for further analysis
by advanced laboratory techniques. 相似文献
8.
9.
10.
Christopher J. Gagliardi Brittany C. Westlake Caleb A. Kent Jared J. Paul John M. Papanikolas Thomas J. Meyer 《Coordination chemistry reviews》2010,254(21-22):2459-2471
In many of the chemical steps in photosynthesis and artificial photosynthesis, proton coupled electron transfer (PCET) plays an essential role. An important issue is how excited state reactivity can be integrated with PCET to carry out solar fuel reactions such as water splitting into hydrogen and oxygen or water reduction of CO2 to methanol or hydrocarbons. The principles behind PCET and concerted electron–proton transfer (EPT) pathways are reasonably well understood. In Photosystem II antenna light absorption is followed by sensitization of chlorophyll P680 and electron transfer quenching to give P680+. The oxidized chlorophyll activates the oxygen evolving complex (OEC), a CaMn4 cluster, through an intervening tyrosine–histidine pair, YZ. EPT plays a major role in a series of four activation steps that ultimately result in loss of 4e?/4H+ from the OEC with oxygen evolution. The key elements in photosynthesis and artificial photosynthesis – light absorption, excited state energy and electron transfer, electron transfer activation of multiple-electron, multiple-proton catalysis – can also be assembled in dye sensitized photoelectrochemical synthesis cells (DS-PEC). In this approach, molecular or nanoscale assemblies are incorporated at separate electrodes for coupled, light driven oxidation and reduction. Separate excited state electron transfer followed by proton transfer can be combined in single semi-concerted steps (photo-EPT) by photolysis of organic charge transfer excited states with H-bonded bases or in metal-to-ligand charge transfer (MLCT) excited states in pre-associated assemblies with H-bonded electron transfer donors or acceptors. In these assemblies, photochemically induced electron and proton transfer occur in a single, semi-concerted event to give high-energy, redox active intermediates. 相似文献