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991.
Daowan LaiYongxin Li Minjuan XuZhiwei Deng Leen van OfwegenPeiyuan Qian Peter ProkschWenhan Lin 《Tetrahedron》2011,67(33):6018-6029
Chemical examination of a Chinese soft coral Sinularia rigida resulted in the isolation and characterization of 19 new cembrane-type diterpenoids, designated as sinulariols A-S (1-19). Their structures were determined on the basis of extensive spectroscopic (2D NMR, IR, and MS) analysis in association with modified Mosher’s method. All compounds featured unusual 19-oxygenated functionalities, which are rarely found from cembranoid family. The biogenetic transformation of the isolated compounds is postulated. Part of the isolated cembranoids showed significant anti-fouling activity. 相似文献
992.
Prof. Dr. Bo Xiao Qian‐Qian Li Yu‐Ting Wang Chun‐Sen Liu Min Hu Shao‐Ming Fang 《无机化学与普通化学杂志》2011,637(2):317-322
A 1D double‐helical coordination polymer {[Cd(pbbm)2]2(ClO4)4(H2O)2}n ( 1 ) was successfully constructed by the reaction of Cd(ClO4)2 · 6H2O with 1,1′‐(1,5‐pentanediyl)bis‐1H‐benzimidazole (pbbm). Interestingly, polymer 1 exhibits highly selective capacity for the ionic exchange of Zn2+ and Cu2+ over Co2+ and Ni2+ ions in the crystalline solid state when the crystals of 1 are immersed in the aqueous solutions of the perchlorate salts of Cu2+, Zn2+, Co2+, and Ni2+ ions, respectively, which indicates that central CdII ion exchange might be considered as being dominated by the coordination ability of metal ions to free functional groups, ionic radii of exchanged metal ions, and the solution concentration of adsorbed metal salts. The parent material‐ and ion‐exchange‐induced products are identified by FT‐IR spectroscopy, PXRD patterns as well as SEM and EDS measurements. In addition, the thermal stability of 1 was also investigated. 相似文献
993.
994.
Electrokinetic particle translocation through a nanopore containing a floating electrode 总被引:1,自引:0,他引:1
Electrokinetic particle translocation through a nanopore containing a floating electrode is investigated by solving a continuum model, composed of the coupled Poisson-Nernst-Planck (PNP) equations for the ionic mass transport and the modified Stokes equations for the flow field. Two effects due to the presence of the floating electrode, the induced-charge electroosmosis (ICEO) and the particle-floating electrode electrostatic interaction, could significantly affect the electrokinetic mobility of DNA nanoparticles. When the electrical double layers (EDLs) of the DNA nanoparticle and the floating electrode are not overlapped, the particle-floating electrode electrostatic interaction becomes negligible. As a result, the DNA nanoparticle could be trapped near the floating electrode arising from the induced-charge electroosmosis when the applied electric field is relatively high. The presence of the floating electrode attracts more ions inside the nanopore resulting in an increase in the ionic current flowing through the nanopore; however, it has a limited effect on the deviation of the current from its base current when the particle is far from the pore. 相似文献
995.
Himstedt HH Yang Q Dasi LP Qian X Wickramasinghe SR Ulbricht M 《Langmuir : the ACS journal of surfaces and colloids》2011,27(9):5574-5581
Presented here is a radically novel approach to reduce concentration polarization and, potentially, also fouling by colloids present in aqueous feeds: magnetically responsive micromixing membranes. Hydrophilic polymer chains, poly(2-hydroxyethyl methacrylate) (PHEMA), were grafted via controlled surface-initiated atom transfer radical polymerization (SI-ATRP) on the surface of polyamide composite nanofiltration (NF) membranes and then end-capped with superparamagnetic iron oxide magnetite (Fe(3)O(4)) nanoparticles. The results of all functionalization steps, that is, bromide ATRP initiator immobilization, SI-ATRP, conversion of PHEMA end groups from bromide to amine, and carboxyl-functional Fe(3)O(4) nanoparticle immobilization via peptide coupling, have been confirmed by X-ray photoelectron spectroscopy (XPS) and field emission scanning electron microscopy (FESEM). These nanoparticles experience a magnetic force as well as a torque under an oscillating external magnetic field. It has been shown, using particle image velocimetry (PIV), that the resulting movement of the polymer brushes at certain magnetic field frequencies induces mixing directly above the membrane surface. Furthermore, it was demonstrated that with such membranes the NF performance could significantly be improved (increase of flux and salt rejection) by an oscillating magnetic field, which can be explained by a reduced concentration polarization in the boundary layer. However, the proof-of-concept presented here for the active alteration of macroscopic flow via surface-anchored micromixers based on polymer-nanoparticle conjugates has much broader implications. 相似文献
996.
Zhou Q Ristenpart WD Stroeve P 《Langmuir : the ACS journal of surfaces and colloids》2011,27(19):11747-11751
We report a magnetic technique for altering the apparent contact angle of aqueous droplets deposited on a nanostructured surface. Polymeric tubes with embedded superparamagnetic magnetite (Fe(3)O(4)) nanoparticles were prepared via layer-by-layer deposition in the 800 nm diameter pores of polycarbonate track-etched (PCTE) membranes. Etching away the original membrane yields a superparamagnetic film composed of mostly vertical tubes attached to a rigid substrate. We demonstrate that the apparent contact angle of pure water droplets deposited on the nanostructured film is highly sensitive to the ante situm strength of an applied magnetic field, decreasing linearly from 117 ± 1.3° at no applied field to 105 ± 0.4° at an applied field of approximately 500 G. Importantly, this decrease in contact angle did not require an inordinately strong magnetic field: a 15° decrease in contact angle was observed even with a standard alnico bar magnet. We interpret the observed contact angle behavior in terms of magnetically induced conformation changes in the film nanostructure, and we discuss the implications for reversibly switching substrates from hydrophilic to hydrophobic via externally tunable magnetic fields. 相似文献
997.
Qian Tang Chengbin Gong Michael Hon-Wah Lam Xiangkai Fu 《Journal of Sol-Gel Science and Technology》2011,59(3):495-504
A photo-responsive molecularly imprinted sol–gel organic-inorganic hybrid material prepared by covalent imprinting of the
template-functional monomer complex formed between 4,4′-dihydroxylazobenzene and ibuprofen was developed to explore the photo-regulated
uptake and release of drug by a silicate-based smart molecularly imprinted materials. After imprinting, the template molecules
(ibuprofen) were removed via hydrolysis in acid, and accurate cavities were left, which could be used as the receptor recognition
sites for ibuprofen. The new organic–inorganic hybrid material shows specific affinity to ibuprofen and reversible uptake
and release of ibuprofen upon alternate irradiation at 365 and 440 nm, respectively. The favorable binding strength of the
imprinted receptor sites in the molecularly imprinted polymer (MIP) for ibuprofen is found to be 2.28 × 103 M−1. Density of receptor sites in the MIP material was 4.0 μmol/g—MIP. 相似文献
998.
Hirotaka Fujita Qingrong Qian Takao Fujii Kazuhiro Mochizuki Akiyoshi Sakoda 《Adsorption》2011,17(5):869-879
A novel bioethanol separation process was proposed in this study employing molecular sieving carbon (MSC) as an adsorbent,
whose pore diameter is close to molecular size of ethanol. In the proposed process, fermentation broth is first introduced
to the adsorption bed packed with MSC. In this step, ethanol is selectively adsorbed onto MSC, with highly enriching ethanol
in the micropore of MSC. Subsequently, the concentrated ethanol is desorbed from MSC to gaseous phase, resulting in further
purification of ethanol owing to a considerable difference in desorption rate between water and ethanol; Because of molecular
sieving effect of MSC, the desorption rate of ethanol is much smaller than that of water. To establish this process, adsorption
equilibrium and kinetics of ethanol on various MSCs were investigated in aqueous phase as the first step. Also, desorption
kinetics of ethanol and water in gaseous phase were investigated. As a result, it was suggested that highly concentrated ethanol
could be obtained with high recovery ratio through these simple operations, meaning the proposed process is quite promising. 相似文献
999.
1000.
This Concept article provides an elementary discussion of a special class of large‐sized gold compounds, so‐called Au nanoclusters, which lies in between traditional organogold compounds (e.g., few‐atom complexes, <1 nm) and face‐centered cubic (fcc) crystalline Au nanoparticles (typically >2 nm). The discussion is focused on the relationship between them, including the evolution from the Au???Au aurophilic interaction in AuI complexes to the direct Au? Au bond in clusters, and the structural transformation from the fcc structure in nanocrystals to non‐fcc structures in nanoclusters. Thiolate‐protected Aun(SR)m nanoclusters are used as a paradigm system. Research on such nanoclusters has achieved considerable advances in recent years and is expected to flourish in the near future, which will bring about exciting progress in both fundamental scientific research and technological applications of nanoclusters of gold and other metals. 相似文献