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Herein, we consider Müller’s spherical, porous, anionic, molybdenum oxide based capsule, (NH4)42‐ [{(MoVI)MoVI5O21(H2O)6}12{MoV2O4(CH3COO)}30]?10 CH3COONH4? 300 H2O≡(NH4)42? 1 a ?crystal ingredients≡ 1 , {Mo132}, as an effective sugar‐decorated nanoplatform for multivalent lectin recognition. The ion‐exchange of NH4+ ions of 1 with cationic‐sugars, D ‐mannose‐ammonium chloride ( 2 ) or D ‐glucose‐ammonium chloride ( 3 ) results in the formation of glyconanocapsules (NH4)42?n 2 n? 1 a and (NH4)42?m 3 m? 1 a . The Mannose (NH4)42?n 2 n? 1 a capsules bind selectively Concanavalin A (Con A) in aqueous solution, giving an association avidity constant of ${K{{{\rm multi}\hfill \atop {\rm a}\hfill}}}$ =4.6×104 M ?1 and an enhancement factor of β=K${{{{\rm multi}\hfill \atop {\rm a}\hfill}}}$ /K${{{{\rm mono}\hfill \atop {\rm ass}\hfill}}}$ =21.9, reminiscent of the formation of “glycoside clusters” on the external surface of glyconanocapsule. The glyconanocapsules (NH4)42?n 2 n? 1 a and (NH4)42?m 3 m? 1 a self‐assemble in “hybrid multilayers” by successive layer‐by‐layer deposition of (NH4)42?n 2 n? 1 a or (NH4)42?m 3 m? 1 a and Con A. These architectures, reminiscent of versatile mimics of artificial tissues, can be easily prepared and quantified by using quartz crystal microgravimetry (QCM). The “biomimetic hybrid multilayers” described here are stable under a continual water flow and they may serve as artificial networks for a greater depth of understanding of various biological mechanisms, which can directly benefit the fields of chemical separations, sensors or storage‐delivery devices.  相似文献   
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The transition to a hydrogen economy requires the development of cost-effective methods for purifying hydrogen from CO. In this study, we explore the possibilities of Cu/ZSM-5 as an adsorbent for this purpose. Samples obtained by cation exchange from aqueous solution (AE) and solid-state exchange with CuCl (SE) were characterized by in situ EPR and FTIR, H2-TPR, CO-TPD, etc. The AE samples possess mainly isolated Cu2+ cations not adsorbing CO. Reduction generates Cu+ sites demonstrating different affinity to CO, with the strongest centres desorbing CO at about 350 °C. The SE samples have about twice higher Cu/Al ratios, as one H+ is exchanged with one Cu+ cation. Although some of the introduced Cu+ sites are oxidized to Cu2+ upon contact with air, they easily recover their original oxidation state after thermal treatment in vacuum or under inert gas stream. In addition, these Cu+ centres regenerate at relatively low temperatures. It is important that water does not block the CO adsorption sites because of the formation of Cu+(CO)(H2O)x complexes. Dynamic adsorption studies show that Cu/ZSM-5 selectively adsorbs CO in the presence of hydrogen. The results indicate that the SE samples are very perspective materials for purification of H2 from CO.  相似文献   
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Natural Aquaporin (AQP) channels are efficient water translocating proteins, rejecting ions. Inspired by this masterpiece of nature, Artificial Water Channels (AWCs) with controlled functional structures, can be potentially used to mimic the AQPs to a certain extent, offering flexible avenues toward biomimetic membranes for water purification. The objective of this paper is to trace the historical development and significant advancements of current reported AWCs. Meanwhile, we attempt to reveal important structural insights and supramolecular self-assembly principles governing the selective water transport mechanisms, toward innovative AWC-based biomimetic membranes for desalination.  相似文献   
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We correct an error in Theorem 12 of the original article concerning the edge scaling limit of the law of real eigenvalues for the real Ginibre ensemble.  相似文献   
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Let (0 < < 1) be the Hölder class on the semi-axis [0,). We characterize the class by rates of approximation of its functions by entire functions of order 1/2 belonging to a special class (similarly to the classical JacksonBernstein theorem). Bibliography: 4 titles.  相似文献   
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