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Nelson A Belitsky JM Vidal S Joiner CS Baum LG Stoddart JF 《Journal of the American Chemical Society》2004,126(38):11914-11922
A self-assembled pseudopolyrotaxane consisting of lactoside-displaying cyclodextrin (CD) "beads" threaded onto a linear polyviologen "string" was investigated for its ability to inhibit galectin-1-mediated T-cell agglutination. The CDs of the pseudopolyrotaxane are able to spin around the axis of the polymer chain as well as to move back and forth along its backbone to alter the presentation of its ligand. This supramolecular superstructure incorporates all the advantages of polymeric structures, such as the ability to span large distances, along with a distinctively dynamic presentation of its lactoside ligands to afford a neoglycoconjugate that can adjust to the relative stereochemistries of the lectin's binding sites. The pseudopolyrotaxane exhibited a valency-corrected 10-fold enhancement over native lactose in the agglutination assay, which was greater than the enhancements observed for lactoside-bearing trivalent glycoclusters and a lactoside-bearing chitosan polymer tested using the same assay. The experimental results indicate that supramolecular architectures, such as the pseudopolyrotaxane, provide tools for investigating protein-carbohydrate interactions. 相似文献
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Measurement of the flux flow noise have been made in foil samples of Pb80In20. The results obtained cannot be explained by previous models which assume direct transit of fluxoids across sample. However, using a model based on the assumption that the flux motion is interrupted by pinning centers it is possible to obtain a good fit to the measured noise curves. Good agreement is also obtained between the calculated and measured critical frequencies using this model. These results may also help explain certain features of noise measurements reported by other workers. 相似文献
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Critical current measurements on a cold rolled Pb60In40 foil show two pinning maxima, one close to Hc2 in the neighborhood of h = 0.95, and the other at low fields around h = 0.15. The high field pinning force maximum shifts to lower fields, and the low field maximum shifts to higher fields with increasing pinning strength. The data is explained in terms of Kramer's pinning force model incorporating Brandt's expression for C>66. 相似文献
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Habibollah Aliabadi Glenn M. Julian S. Jha W. C. H. Joiner J. P. Wang 《Hyperfine Interactions》1994,94(1):2029-2033
Sr
x
Ca1–x
Cu0.99
57Fe0.01O2 was studied forx=0.13, 0.15, and 0.17. Mössbauer spectroscopy and magnetization measurements indicate magnetic ordering characteristic of spin glass systems withT
f70K forx=0.15 and 0.13. 相似文献
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Correlations are observed between reductions in the critical current and the superconducting flux flow noise power as a deformed Pb80In20 foil undergoes room temperature annealing, thus providing evidence that the noise originates from local interactions between moving fluxoids and pinning centers. 相似文献
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Navzer Sachinvala D. V. Parikh Paul Sawhney SeChin Chang Jerzey Mirzawa William Jarrett Beth Joiner 《先进技术聚合物》2007,18(8):620-628
In this paper we discuss the preparation and comparative evaluation of silver (I) [Ag(I)] nonwoven and woven antimicrobial barrier fabrics generated from commercial calcium‐sodium alginates and laboratory prepared sodium carboxymethyl (CM) cotton nonwovens and CM‐cotton printcloth for potential use as wound dressings. Degrees of CM substitution (DS) in cotton nonwoven and printcloth samples by titrimetry were 0.38 and 0.10, respectively. Coordination of Ag(I) with carboxylates on fabrics was effected by ion exchange and nitrates were removed by washing to mitigate nitrate ion toxicity issues. Durability of silver coordinated fabrics was tested by soaking them in deionized water with slight agitation at 50°C. Ag(I) alginates and nonwoven Ag(I)‐CM‐cottons lost structural integrity in water. Ag‐CM‐cotton printcloth samples retained structural integrity even after four soak‐and‐dry cycles, were smooth to the touch when dry, and were smoother when moistened. They could be easily peeled from wound surfaces without inducing trauma. Solid‐state carbon‐13 (13C) nuclear magnetic resonance (NMR) spectrometry was used to observe changes in carbonyl resonances in Ag(I) alginates and Ag(I)‐CM‐printcloth, and the chemical shift positions of carbonyl resonances of uncoordinated and Ag(I) coordinated fabrics did not change. Inductively coupled plasma‐mass spectrometry (ICP‐MS) was used following fabric digestion to determine the total Ag(I) ion content in fabrics. Ag(I) alginates were found to hold about 10–50 mg Ag(I) per gram fabric; and Ag(I) cotton woven and nonwoven fabrics held about 5–10 mg Ag(I) ions per gram fabric. Kinetic release of Ag(I) after soaking once in physiological saline was studied with ICP‐MS to estimate the availability of Ag(I) upon a single exchange with Na(I) ions on wound surfaces. Alginates released between ~13 and 28% of coordinated Ag(I), and CM‐cotton nonwovens and CM‐cotton printcloth released ~14 and 3% of coordinated Ag(I) ions, respectively. Finally, Ag(I) alginates and Ag(I)‐CM‐cotton printcloth samples were evaluated against Gram‐positive Staphylococcus aureus and Gram‐negative Klebsiella pneumoniae. Ag(I) alginates suppressed 99.95% of bacterial growth in vitro. Even after four soak‐and‐dry cycles in deionized water Ag(I)‐CM‐cotton printcloth suppressed 99.99% of bacterial growth in vitro. Published in 2007 by John Wiley & Sons, Ltd. 相似文献
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Experimental flux flow V-I characteristics are compared with our previous model which assumes flux motion is interrupted by local pinning interactions. Quantitative changes in these characteristics occur at the field at which the peak in the pinning force occurs. 相似文献
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The imine bond--formed by the reversible condensation of an amine and an aldehyde--and its applications as a dynamic covalent bond in the template-directed synthesis of molecular compounds, will be the focus of this tutorial review. Template-directed synthesis--or expressed another way, supramolecular assistance to covalent synthesis--relies on the use of reversible noncovalent bonding interactions between molecular building blocks in order to preorganise them into a certain relative geometry as a prelude to covalent bond formation to afford the thermodynamically preferred product. The use of this so-called dynamic covalent chemistry (DCC) in templated reactions allows for an additional amount of reversibility, further eliminating potential kinetic products by allowing the covalent bonds that are formed during the template-directed reaction to be 'proofread for errors', thus making it possible for the reaction to search out its thermodynamic minimum. The marriage of template-directed synthesis with DCC has allowed chemists to construct an increasingly complex collection of compounds from relatively simple precursors. This new paradigm in organic synthesis requires that each individual piece in the molecular self-assembly process is preprogrammed so that the multiple recognition events expressed between the pieces are optimised in a highly cooperative manner in the desired product. It offers an extremely simple way of making complex mechanically interlocked compounds--e.g., catenanes, rotaxanes, suitanes, Borromean rings and Solomon knots--from relatively simple precursors. 相似文献