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61.
Being able to bind, select, and transport species is central to a number of fields, including medicine, materials, and environmental science. In particular, recognizing a specific species from one phase and transporting it across, or into another phase, has obvious applications in environ-mental science, for example, removal of unwanted or toxic materials from an aqueous or organic phase. In this paper, we describe an approach that uses a functionalized dendritic polymer to bind and transport a small anionic molecule across an organic phase (and between two aqueous phases). The design was based on encapsulation principles borrowed from nature, where anions are bound and transported by proteins that have specific sites within their globular ordered structures. For the work reported here, a globular dendritic polymer functionalized with an isophthalamide-based receptor was used to replace the protein structure and anion-binding site. Along with control experiments, the binding and transport properties of two functionalized HBPs were assessed using a Pressman U tube experiment. Both HBPs demonstrated an enhanced ability to bind and transport anions (when compared to the anion-binding site used in isolation). Furthermore, optimum binding and transport occurred when the smaller of the two HBPs were used. This supports our previous observations regarding the existence of a dense packed limit for HBPs. 相似文献
62.
Egan L Kamenev K Papanikolaou D Takabayashi Y Margadonna S 《Journal of the American Chemical Society》2006,128(18):6034-6035
The flexibility of the structure of Prussian blue analogues and its ability to incorporate a variety of competing magnetic interactions have allowed the design of mixed ferro-ferrimagnets, which span the whole spectrum of magnetic behavior, including the rare phenomenon of magnetization reversal in response to a change in temperature. Hydrostatic pressure is used here to induce multiple reversals of the direction of the spontaneous magnetization in the trimetallic Prussian blue analogue, Rb0.64Ni0.31Mn0.87[Fe(CN)6].2.8H2O. Remarkably, the magnetic response is extremely sensitive to pressure, and the magnetization flips from positive to negative and back to positive in a very narrow pressure range (0 < P < 0.6 kbar). A further increase in pressure to 4.0 kbar induces an internal redox reaction, and the magnetic order switches from ferrimagnetic to bulk ferromagnetism. 相似文献
63.
Papanikolaou D Margadonna S Kosaka W Ohkoshi S Brunelli M Prassides K 《Journal of the American Chemical Society》2006,128(25):8358-8363
The effect of X-ray illumination on the structural properties of the mixed valence Prussian blue analogue CsFe(II)[Cr(III)(CN)6] has been studied by time-dependent high-resolution synchrotron X-ray diffraction. Abrupt isosymmetric phase transitions, accompanied by dramatic volume collapse, were found in the temperature range 245-265 K, induced by sudden Fe(II) spin transitions from the high spin (HS) (4t(2g)2e(g), S = 2) to the low spin (LS) (6t(2g)0e(g), S = 0) configuration. Absorption of X-ray photons generates photoexcited Fe(II)(LS) domains whose size rapidly grows with time until the percolation threshold is reached and the structure collapse is triggered. The persistent character of the optically excited spin crossover states derives from the strong electron-phonon coupling, associated with the large lattice relaxations, which accompany the internal spin rearrangements. It is thus possible to use X-ray light in a controllable and efficient way to induce photoswitching between the ground and hidden or inaccessible excited states in suitably selected multistable materials in the bulk. 相似文献
64.
Mouchlis VD Melagraki G Mavromoustakos T Kollias G Afantitis A 《Journal of chemical information and modeling》2012,52(3):711-723
Molecular docking, classification techniques, and 3D-QSAR CoMSIA were combined in a multistep framework with the ultimate goal of identifying potent pyrimidine-urea inhibitors of TNF-α production. Using the crystal structure of p38α, all the compounds were docked into the enzyme active site. The docking pose of each compound was subsequently used in a receptor-based alignment for the generation of the CoMSIA fields. "Active" and "inactive" compounds were used to build a Random Tree classification model using the docking score and the CoMSIA fields as input parameters. Domain of applicability indicated the compounds for which activity estimations can be accepted with confidence. For the active compounds, a 3D-QSAR CoMSIA model was subsequently built to accurately estimate the IC(50) values. This novel multistep framework gives insight into the structural characteristics that affect the binding and the inhibitory activity of these analogues on p38α MAP kinase, and it can be extended to other classes of small-molecule inhibitors. In addition, the simplicity of the proposed approach provides expansion to its applicability such as in virtual screening procedures. 相似文献
65.
66.
Georgia‐Paraskevi Nikoleli Muhammad Q. Israr Nikolaos Tzamtzis Dimitrios P. Nikolelis Magnus Willander Nikolas Psaroudakis 《Electroanalysis》2012,24(6):1285-1295
The present article describes a miniaturized potentiometric urea lipid film based biosensor on graphene nanosheets. Structural characterization of graphene nanosheets for miniaturization of potentiometric urea lipid film based biosensors have been studied through atomic force microscopy (AFM) and transmission electron microscopy (TEM) measurements. UV‐Vis and Fourrier transform IR (FTIR) spectroscopy have been utilized to study the pre‐ and postconjugated surfaces of graphene nanosheets. The presented potentiometric urea biosensor exhibits good reproducibility, reusability, selectivity, rapid response times (~4 s), long shelf life and high sensitivity of ca. 70 mV/decade over the urea logarithmic concentration range from 1×10?6 M to 1×10?3 M. 相似文献
67.
George Ioannou Gregory Prastacos Georgia Skintzi 《Annals of Operations Research》2004,126(1-4):195-213
In this paper we address the problem of inventory positioning, i.e., the determination of the supply chain node where inventory should be held, to minimize holding costs given a pre-specified order fill rate. A single-echelon inventory system with multiple products models the problem. The value of inventory is assumed to be an increasing function of the amount of processing performed at upstream nodes, while achieved fill-rates are dependent on the distance or time between the inventory storage and customer locations. We propose a novel analytical approach to solve the problem for the case of normally distributed demand that is based on iterative calculations of inventory holding costs at the various potential inventory locations. 相似文献
68.
69.
George Linardatos Georgia Tsoukleri John Parthenios Costas Galiotis Orietta Monticelli Saverio Russo Constantinos Tsitsilianis 《Macromolecular rapid communications》2011,32(4):371-377
In this communication an extended “in–out” polymerization method is presented, which leads to the synthesis of novel heteroarm star block terpolymers of the type An(B‐b‐C)n. A four step/one‐pot synthetic procedure is pursued using anionic polymerization under an inert atmosphere. The resulted star‐shaped terpolymer consists of a divinyl benzene nodule bearing pure polystyrene and poly(hexyl methacrylate)‐block‐poly(methyl methacrylate) diblock copolymer arms. It is shown that this kind of star terpolymers can self‐assemble in the bulk forming lamellae mesophase by arm and block segregation. The mechanical properties of the terpolymer have been examined in detail. Finally, the proposed synthetic procedure can be easily employed in other controlled polymerization methods.
70.
Georgia M. Arvanitis Michael E. Berardini Douglas M. Ho 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(3):m126-m128
The title complex [systematic name: trans‐bis(3‐isopropyl‐7‐oxocyclohepta‐1,3,5‐trienolato)copper(II)], [Cu(C10H11O2)2],is a substance possessing antimicrobial activity. The compound crystallizes in a number of polymorphic forms, the structures for two of which are reported here. Stacks of square‐planar molecules exhibiting weak intermolecular copper–olefin π interactions (not observed in earlier reports on this substance) are described. The molecules have crystallographically imposed inversion symmetry, with stacking and copper–olefin π distances ranging from 3.226 (2) to 3.336 (1) Å. 相似文献