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Extraction behaviors of catecholamines with a series of calixarene carboxylic acid derivatives were investigated. Relatively large calix[6]arene and calix[8]arene extract catecholamines into the organic solution, while smaller calix[4]arene and the monomer analog do not. The calix[6]arene, which has a cavity that fits a protonated amino group well, selectively extracts a primary amino compound dopamine over other catecholamines. Slope analysis and Job’s method confirmed formation of a 1:1 complex between the calix[6]arene and dopamine. On the other hand, the calix[8]arene extracts both dopamine and adrenaline, due to the large cavity for induced-fit recognition. Dopamine extracted with the calixarene is quantitatively stripped by contacting the organic solution with a fresh acidic solution.  相似文献   
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A study on the adsorption characteristics of Pb(II) and Cr(III) cations onto C‐4‐methoxyphenylcalix‐[4]resorcinarene (CMPCR) in batch and fixed bed column systems has been conducted. CMPCR was produced by one step synthesis from resorcinol, 4‐methoxybenzaldehyde, and HCl. The synthesis was carried out at 78 °C for 24 hours and afforded the adsorbent in 85.7% as a 3:2 mixture of C:C isomer. Most parameters in batch and fixed bed column systems confirm that CMPCR is a good adsorbent for Pb(II) and Cr(III), though Pb(II) adsorption was more favorable than that of Cr(III). The adsorption kinetic of Pb(II) and Cr(III) adsorptions in batch and fixed bed column systems followed a pseudo 2n order kinetics model. The rate constant of Pb(II) was higher than that of Cr(III) in the batch system, but this result was contrary to the result obtained in a fixed bed column system. Desorption studies to recover the adsorbed Pb(II) and Cr(III) were performed sequentially with distilled water and HCl, and the results showed that the adsorption was dominated by chemisorption.  相似文献   
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A cone confomational p-t-octylcalix[4]arene with four methylenephosphonic acids at the lower rim as well as its monomeric analog have been synthesized as a new extraction reagent to investigate the extraction behavior of the nine trivalent rare earth elements: Y, La, Pr, Nd, Sm, Eu, Gd, Ho and Er. The new calix[4]arene exhibited significantly higher extraction capacity than not only the monomeric derivative and the commercial extraction reagent, 2-ethylhexyl hydrogen 2-ethylhexylphosphonate, but also the cone conformational calix[4]arene extractants employed in our previous work, composed of a tetrapropylenephosphonic acid with a longer spacer, a tetraphosphonic acid at the upper rim, and tetraacetic acid at the lower rim. A dependence on the pH was observed for the new extractant in the highly acidic region, and the extraction took place via a simple ion-exchange mechanism. Using slope analysis, the stoichiometries of tetrameric and monomeric extractants to rare earth metal ions were determined to be 2:1 and 3:1, respectively. Using the proposed extraction equations, extraction equilibrium constants and separation factors were estimated. The extremely high extraction ability and moderate separation efficiency were attributed to the chelating effect of the phosphonic acid and the phenoxy oxygen atom. The effect of the phenoxy oxygen atom on extraction ability and separation efficiency of calix[4]arene derivatives was found to be significant.  相似文献   
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The notion of a toric origami manifold, which weakens the notion of a symplectic toric manifold, was introduced by A. Cannas da Silva, V. Guillemin and A.R. Pires. They showed that toric origami manifolds bijectively correspond to origami templates via moment maps, where an origami template is a collection of Delzant polytopes with some folding data. Like a fan is associated to a Delzant polytope, a multi-fan introduced by A. Hattori and M. Masuda can be associated to an oriented origami template. In this paper, we discuss their relationship and show that any simply connected compact smooth 4-manifold with a smooth action of T 2 can be a toric origami manifold. We also characterize products of even dimensional spheres which can be toric origami manifolds.  相似文献   
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Several rigidity problems in toric topology are addressed in the survey paper by the second and third authors, “Classification Problems of Toric Manifolds via Topology” (in Toric Topology, Am. Math. Soc., Providence, RI, 2008, pp. 273–286). In the present paper, we survey the results on those problems including recent developments.  相似文献   
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Adhikari BB  Gurung M  Kawakita H  Ohto K 《The Analyst》2011,136(21):4570-4579
The solvent extraction behavior of multiple proton ionizable p-tert-butylcalix[4]arene and [6]arene carboxylic acid derivatives towards indium has been investigated along with an acyclic monomeric analogue from weakly acidic media into chloroform. The extraction mechanism is ion exchange and carboxylic acid groups are adequate ligating sites for extraction. The cyclic structure of calixarene ligands to accommodate the potential guest species and the cooperativity effect of multifunctional groups significantly affect the complexation behavior and calixarene derivatives are found to be excellent extractants over the monomeric analogue. The composition of the extracted complex depends on the solution pH and attempts to determine the composition of the extracted complex for the extraction of indium have been stymied by complications arising from the formation of polynuclear species of indium and bridged polymeric species of calixarene carboxylic acid derivatives. One mole of calix[4]arene derivative extracts 2.5 moles of indium whereas the calix[6]arene derivative tends to extract 4.0 moles of indium. The loaded indium is back extracted with 1 mol dm(-3) hydrochloric acid solution. Though quantitative back extraction of indium was achieved from the fully loaded calix[6]arene derivative, it was only achieved up to 85% in the case of the calix[4]arene derivative.  相似文献   
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The permeation fluxes of phenol, benzene sulfonate (BS) and benzene disulfonate (BDS) through a porous anodic alumina membrane with the perpendicularly oriented silica-surfactant nanochannel assembly membrane (NAM) were measured in water-ethanol mixture media. The permeation flux depended on solute charges and on solvent composition. As the ethanol ratio increased, the fluxes of BS and BDS increased and the flux of phenol decreased. The results of extraction/elution experiments also depended on the solute charges and the solvent composition. Chromatographic experiments in n-hexane showed that dipole and hydrophobic interactions affect the retention of solutes. Permeation of the solute across the NAM in water-ethanol mixture is likely to be determined by various factors such as dipole interaction, hydrophobic interaction, solvation, and anion-exchange efficiencies.  相似文献   
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