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The self-assembly characteristics in aqueous solutions of cationic bolaamphiphiles with systematic changes in their chemical structure is described with respect to their interfacial properties within water and at the air/water interface. Six cationic bolaamphiphiles were synthesized from multifunctional vernonia oil with the following variations: (a) two different alkyl chain lengths connecting the head groups, (b) polar ester or hydrogen bonding amide groups within the hydrophobic domain, and (c) an acetylcholine cationic head group with different conjugation sites to the alkyl chain. Surface tension measurements were used for determining critical aggregation concentration (CAC) values and air/water interfacial parameters such as 'effectiveness', surface excess concentration and area occupied by one molecule in the air/water interface. Fluorescent studies with pyrene were used to characterize CAC properties within the aqueous volume and transmission electron microscopy (TEM) for determining the aggregate structure's size, homogeneity and morphology. A bolaamphiphile molecular structure vs. interfacial property relationship was derived from this data which could be used to determine the molecular structure properties needed to generate interfacial forces to form either spherical vesicles or fibrous networks. The effects of the aliphatic chain length, head group orientation and functional groups within the hydrophobic domain on CAC, surface tension properties and self-aggregate morphology are described. Most bolaamphiphiles studied had CAC values in the 10-190 μM range, while two out of the six were found to assemble into MLM spherical vesicles with diameters ranging up to 120 nm suitable for drug delivery applications. Others formed a gelatinous network of fibers or multi-lamellar vesicles. 相似文献
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Let
be a dense sub-semigroup of ℝ+, and let X be a separable, reflexive Banach space. This note contains a proof that every weakly continuous contractive semigroup of
operators on X over
can be extended to a weakly continuous semigroup over ℝ+. We obtain similar results for nonlinear, nonexpansive semigroups as well. As a corollary we characterize all densely parametrized
semigroups which are extendable to semigroups over ℝ+.
O.M. Shalit was partially supported by the Gutwirth Fellowship. 相似文献
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Eliahu Cohen Yair Avny Albert Zilkha 《Journal of polymer science. Part A, Polymer chemistry》1971,9(6):1469-1479
The anionic graft polymerization of propylene sulfide on cellulose membrane was studied. Alkali cellulosates were used to initiate graft polymerization, and graft polymers of high polypropylene sulfide content were obtained in good yields. The graft polymerization was accompanied by a certain extent of homopolymerization. The effects of reaction solvent, monomer concentration, cellulosate degree of substitution, and type of the alkali metal cellulosate on the graft polymer composition, yield, and on the molecular weight of the grafted side chains were investigated. 相似文献
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A method for enzymatic determination of pyridostigmine is considered. The nonlinear calibration graphs obtained are functions of nine independent variables. The optimization of the curves is discussed, with the relative error as the criterion of optimization. A graphical method is suggested, which allows easy determination of the relative error, of the best concentration for sampling, and of the limit of response. A shortcut method of optimization for asymptotic calibration curves is suggested, and illustrated by optimizing the time of hydrolysis of acetylcholine by cholinesterase. Some determinations of pyridostigmine in water, urine and bovine serum are presented, employing the suggested method. 相似文献
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Eliahu Cohen Yair Avny Albert Zilkha 《Journal of polymer science. Part A, Polymer chemistry》1971,9(6):1481-1492
The adsorption of iodine, silver nitrate, and mercuric chloride by cellulosic membranes grafted with polypropylene sulfide was investigated. It was found that the grafted polypropylene sulfide adsorbed iodine by complexation from aqueous solution or from gaseous phase. Adsorption from water led to the formation of a complex with molar ratio of I2 to propylene sulfide units of 1, and that while the complex formed from gaseous iodine had a molar ratio I2 to propylene sulfide approaching 2. Most of the sulfide groups participated in complexation. It was found that the complexation of the polysulfide was accompanied by degradation which was attributed to halogenation of the polysulfide at the tertiary carbon atoms. The iodine complex was more stable in water than in organic solvents, where most of the iodine was desorbed. The graft polymers adsorbed also by complexation silver nitrate and mercuric chloride. Adsorption could be described by a Freundlich type isotherm. At low concentrations most of the silver nitrate present in solution was adsorbed. 相似文献
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A Gedanken experiment is presented where an excited and a ground-state atom are positioned such that, within the former’s half-life time, they exchange a photon with 50% probability. A measurement of their energy state will therefore indicate in 50% of the cases that no photon was exchanged. Yet other measurements would reveal that, by the mere possibility of exchange, the two atoms have become entangled. Consequently, the “no exchange” result, apparently precluding entanglement, is non-locally established between the atoms by this very entanglement. This quantum-mechanical version of the ancient Liar Paradox can be realized with already existing transmission schemes, with the addition of Bell’s theorem applied to the no-exchange cases. Under appropriate probabilities, the initially-excited atom, still excited, can be entangled with additional atoms time and again, or alternatively, exert multipartite nonlocal correlations in an interaction free manner. When densely repeated several times, this result also gives rise to the Quantum Zeno effect, again exerted between distant atoms without photon exchange. We discuss these experiments as variants of interaction-free-measurement, now generalized for both spatial and temporal uncertainties. We next employ weak measurements for elucidating the paradox. Interpretational issues are discussed in the conclusion, and a resolution is offered within the Two-State Vector Formalism and its new Heisenberg framework. 相似文献
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David E. Portlock Anil C. Ghosh William E. Schwarzel Richard R. Kurtz Eliahu Boger Haldean C. Dalzell Raj K. Razdan 《Journal of heterocyclic chemistry》1976,13(4):781-788
Novel cyclol derivatives (Table 1, 15, 16 ) similar in structure to the peptide portion of ergocornine were synthesized. Detailed experimental procedures are given for the preparation of the cis- 13a and the unknown trans- 14a cyclol esters. 相似文献
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