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131.
Dr. Allison M. Latshaw Dr. W. Michael Chance Dr. Gregory Morrison Karl D. zur Loye Branford O. Wilkins Mark D. Smith Dr. Pamela S. Whitfield Dr. Melanie J. Kirkham Dr. Sebastian A. Stoian Prof. Dr. Hans‐Conrad zur Loye 《Angewandte Chemie (International ed. in English)》2016,55(42):13195-13199
Crystals of the first sodalite‐type zeolite containing an all‐iron framework, a ferrolite, Ba8(Fe12O24)Nay(OH)6?x H2O, were synthesized using the hydroflux method in nearly quantitative yield. Ba8(Fe12O24)Nay(OH)6?x H2O crystallizes in the cubic space group with a=10.0476(1) Å. Slightly distorted FeO4 tetrahedra are linked to form Fe4O4 and Fe6O6 rings, which in turn yield channels and internal cavities that are characteristic of the sodalite structure. Barium, sodium, and hydroxide ions and water molecules are found in the channels and provide charge balance. Magnetic measurements indicate that the ferrolite exhibits magnetic order up to at least 700 K, with the field‐cooled and zero‐field‐cooled curves diverging. Analysis of the 57Fe Mössbauer spectra revealed two spectral components that have equal spectral areas, indicating the presence of two subsets of iron centers in the structure. Dehydrated versions of the ferrolite were also prepared by heating the sample. 相似文献
132.
Quantitative,In Situ Visualization of Metal‐Ion Dissolution and Transport Using 1H Magnetic Resonance Imaging 下载免费PDF全文
Dr. Joshua M. Bray Prof. Alison J. Davenport Prof. Karl S. Ryder Dr. Melanie M. Britton 《Angewandte Chemie (International ed. in English)》2016,55(32):9394-9397
Quantitative mapping of metal ions freely diffusing in solution is important across a diverse range of disciplines and is particularly significant for dissolution processes in batteries, metal corrosion, and electroplating/polishing of manufactured components. However, most current techniques are invasive, requiring sample extraction, insertion of an electrode, application of an electric potential or the inclusion of a molecular sensor. Thus, there is a need for techniques to visualize the distribution of metal ions non‐invasively, in situ, quantitatively, in three dimensions (3D) and in real time. Here we have used 1H magnetic resonance imaging (MRI) to make quantitative 3D maps showing evolution of the distribution of Cu2+ ions, not directly visible by MRI, during the electrodissolution of copper, with high sensitivity and spatial resolution. The images are sensitive to the speciation of copper, the depletion of dissolved O2 in the electrolyte and show the dissolution of Cu2+ ions is not uniform across the anode. 相似文献
133.
Jackson T Woo LW Trusselle MN Chander SK Purohit A Reed MJ Potter BV 《Organic & biomolecular chemistry》2007,5(20):2940-2952
The synthesis and biological evaluation of a series of novel Dual Aromatase-Sulfatase Inhibitors (DASIs) are described. It is postulated that dual inhibition of the aromatase and steroid sulfatase enzymes, both responsible for the biosynthesis of oestrogens, will be beneficial in the treatment of hormone-dependent breast cancer. The compounds are based upon the Anastrozole aromatase inhibitor template which, while maintaining the haem ligating triazole moiety crucial for enzyme inhibition, was modified to include a phenol sulfamate ester motif, the pharmacophore for potent irreversible steroid sulfatase inhibition. Adaption of a synthetic route to Anastrozole was accomplished via selective radical bromination and substitution reactions to furnish a series of aromatase inhibitory pharmacophores. Linking these fragments to the phenol sulfamate ester moiety employed SN2, Heck and Mitsunobu reactions with phenolic precursors, from where the completed DASIs were achieved via sulfamoylation. In vitro, the lead compound, 11, had a high degree of potency against aromatase (IC50 3.5 nM), comparable with that of Anastrozole (IC50 1.5 nM) whereas, only moderate activity against steroid sulfatase was found. However, in vivo, 11 surprisingly exhibited potent dual inhibition.Compound 11 was modelled into the active site of a homology model of human aromatase and the X-ray crystal structure of steroid sulfatase. 相似文献
134.
Jackson T Woo LW Trusselle MN Chander SK Purohit A Reed MJ Potter BV 《Organic & biomolecular chemistry》2007,5(18):2940-2952
The synthesis and biological evaluation of a series of novel Dual Aromatase-Sulfatase Inhibitors (DASIs) are described. It is postulated that dual inhibition of the aromatase and steroid sulfatase enzymes, both responsible for the biosynthesis of oestrogens, will be beneficial in the treatment of hormone-dependent breast cancer. The compounds are based upon the Anastrozole aromatase inhibitor template which, while maintaining the haem ligating triazole moiety crucial for enzyme inhibition, was modified to include a phenol sulfamate ester motif, the pharmacophore for potent irreversible steroid sulfatase inhibition. Adaption of a synthetic route to Anastrozole was accomplished via selective radical bromination and substitution reactions to furnish a series of inhibitory aromatase pharmacophores. Linking these fragments to the phenol sulfamate ester moiety employed S(N)2, Heck and Mitsunobu reactions with phenolic precursors, from where the completed DASIs were achieved via sulfamoylation. In vitro, the lead compound, 11, had a high degree of potency against aromatase (IC(50) 3.5 nM), comparable with that of Anastrozole (IC(50) 1.5 nM) whereas, only moderate activity against steroid sulfatase was found. However, in vivo, 11 surprisingly exhibited potent dual inhibition. Compound 11 was modelled into the active site of a homology model of human aromatase and the X-ray crystal structure of steroid sulfatase. 相似文献
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138.
Preparation and coordination complex of the first imine-bridged tetrathiafulvalene-pyridine donor ligand 总被引:1,自引:0,他引:1
Chahma M Hassan N Alberola A Stoeckli-Evans H Pilkington M 《Inorganic chemistry》2007,46(10):3807-3809
The first imine-bridged pyridyltetrathiafulvalene building block (TTF-CH=N-Py, 1) has been synthesized via the Schiff base condensation of formyltetrathiafulvalene and 2-aminopyridine. The preparation, X-ray crystal structure, electrochemical and magnetic characterization of a 1:1 copper complex [CuII(hfac)2(TTF-CH=N-Py)] (2) are reported. The crystal structure reveals that the imine N atom participates in chelation to the paramagnetic center, thus making this ligand an attractive precursor for the assembly of pi-d systems. 相似文献
139.
Perkell JS Denny M Lane H Guenther F Matthies ML Tiede M Vick J Zandipour M Burton E 《The Journal of the Acoustical Society of America》2007,121(1):505-518
The role of auditory feedback in speech production was investigated by examining speakers' phonemic contrasts produced under increases in the noise to signal ratio (N/S). Seven cochlear implant users and seven normal-hearing controls pronounced utterances containing the vowels /i/, /u/, /e/ and /ae/ and the sibilants /s/ and /I/ while hearing their speech mixed with noise at seven equally spaced levels between their thresholds of detection and discomfort. Speakers' average vowel duration and SPL generally rose with increasing N/S. Average vowel contrast was initially flat or rising; at higher N/S levels, it fell. A contrast increase is interpreted as reflecting speakers' attempts to maintain clarity under degraded acoustic transmission conditions. As N/S increased, speakers could detect the extent of their phonemic contrasts less effectively, and the competing influence of economy of effort led to contrast decrements. The sibilant contrast was more vulnerable to noise; it decreased over the entire range of increasing N/S for controls and was variable for implant users. The results are interpreted as reflecting the combined influences of a clarity constraint, economy of effort and the effect of masking on achieving auditory phonemic goals-with implant users less able to increase contrasts in noise than controls. 相似文献
140.