Atom aqueous

The reaction is applicable to the preparation of amines from amides of aliphatic aromatic, aryl-aliphatic and heterocyclic acids. A further example is given in Section IV,170 in connexion with the preparation of anthranilic acid from phthal-imide. It may be mentioned that for aliphatic monoamides containing more than eight carbon atoms aqueous alkaline hypohalite gives poor yields of the amines. Good results are obtained by treatment of the amide (C > 8) in methanol with sodium methoxide and bromine, followed by hydrolysis of the resulting N-alkyl methyl carbamate ... 

From the result of Henglein and Gutierrez (162), Mills et al. estimated a value of —1.3 V for the S/SH couple, in which S apparently refers to dissolved S8 (218). If we use Pearson s result for HS and estimate the hydration free energy of atomic sulfur as 16.4 kj/mol, the value for Ar, we obtain a potential of 1.44 V for reduction of atomic aqueous sulfur to HS. 

J. S. Merola, Variation of Central Atoms, Aqueous-Phase Organometallic Catalysis , ed., B. Comils and W. A. Herrmann, Wiley-VCH Verlag GmbH, 1998, p. 59. 

This section discusses the different reactivity of aqueous Fe(II) and Mn(II) by 02. Both metal ions and 02 are formally Lewis acids. This chemical behavior suggests that reactivity may be slow if inner-sphere processes are important. As shown below, Fe(II) oxidation can occur via outer-sphere processes, whereas Mn(II) oxidation must occur via inner-sphere processes. For these oxidation reactions to be facile, it is necessary to enhance the metal ion s ability to lose an electron (become a reducing agent or a base ). This can be accomplished with the appropriate ligating atoms. Aqueous Fe(II) and Mn(II) are both labile cations with d6 and d5 (t2ge2) electron configurations, respectively. This... 

The thiosulfate anion, a soft base, strongly coordinates Ag" ", a soft Lewis acid through the terminal sulfur atom. Aqueous sodium thiosulfate ( hypo ), Na2S203, is therefore used to remove unchanged AgBr from exposed photographic film. The process is called as... 

The use of thermal inkjet spray freeze-drying for fabrication of in-halable, excipient-free salbutamol sulfate was investigated (86). A modified Hewlett-Packard printer was used to atomize aqueous salbutamol sulfate solutions into liquid nitrogen. Then, the frozen droplets were subjected to freeze-drying. 

Notes Also beads, prilled, atomized, aqueous dispersion ... 

Figure 3.3 (on the previous page) shows the electron-dot formulas of the four oxyacids of chlorine. Notice that all of the oxygen atoms are bonded to the chlorine atom. Each hydrogen atom is bonded to an oxygen atom. Aqueous solutions of these molecules are acids because the O-H bonds are broken as the hydrogen is pulled away by water molecules. 

The density of heavy fuels is greater than 0.920 kg/1 at 15°C. The marine diesel consumers focus close attention on the fuel density because of having to centrifuge water out of the fuel. Beyond 0.991 kg/1, the density difference between the two phases —aqueous and hydrocarbon— becomes too small for correct operation of conventional centrifuges technical improvements are possible but costly. In extreme cases of fuels being too heavy, it is possible to rely on water-fuel emulsions, which can have some advantages of better atomization in the injection nozzle and a reduction of pollutant emissions such as smoke and nitrogen oxides. 

This interface is critically important in many applications, as well as in biological systems. For example, the movement of pollutants tln-ough the enviromnent involves a series of chemical reactions of aqueous groundwater solutions with mineral surfaces. Although the liquid-solid interface has been studied for many years, it is only recently that the tools have been developed for interrogating this interface at the atomic level. This interface is particularly complex, as the interactions of ions dissolved in solution with a surface are affected not only by the surface structure, but also by the solution chemistry and by the effects of the electrical double layer [31]. It has been found, for example, that some surface reconstructions present in UHV persist under solution, while others do not. 

The hydration of more inert ions has been studied by O labelling mass spectrometry. 0-emiched water is used, and an equilibrium between the solvent and the hydration around the central ion is first attained, after which the cation is extracted rapidly and analysed. The method essentially reveals the number of oxygen atoms that exchange slowly on the timescale of the extraction, and has been used to establish the existence of the stable [1 10304] cluster in aqueous solution. 

Biggs S, Mulvaney P, Zukoski C F and Grieser F 1994 Study of anion adsorption at the gold-aqueous solution interface by atomic force microscopy J. Am. Chem. Soc. 116 9150... 

A selection of important anionic surfactants is displayed in table C2.3.1. Carboxylic acid salts or tire soaps are tire best known anionic surfactants. These materials were originally derived from animal fats by saponification. The ionized carboxyl group provides tire anionic charge. Examples witlr hydrocarbon chains of fewer tlran ten carbon atoms are too soluble and tliose witlr chains longer tlran 20 carbon atoms are too insoluble to be useful in aqueous applications. They may be prepared witlr cations otlrer tlran sodium. 

The alkali metals have the interesting property of dissolving in some non-aqueous solvents, notably liquid ammonia, to give clear coloured solutions which are excellent reducing agents and are often used as such in organic chemistry. Sodium (for example) forms an intensely blue solution in liquid ammonia and here the outer (3s) electron of each sodium atom is believed to become associated with the solvent ammonia in some way, i.e. the system is Na (solvent) + e" (sohem). 

The method has severe limitations for systems where gradients on near-atomic scale are important (as in the protein folding process or in bilayer membranes that contain only two molecules in a separated phase), but is extremely powerful for (co)polymer mixtures and solutions [147, 148, 149]. As an example Fig. 6 gives a snapshot in the process of self-organisation of a polypropylene oxide-ethylene oxide copolymer PL64 in aqueous solution on its way from a completely homogeneous initial distribution to a hexagonal structure. 

Although extraction of lipids from membranes can be induced in atomic force apparatus (Leckband et al., 1994) and biomembrane force probe (Evans et al., 1991) experiments, spontaneous dissociation of a lipid from a membrane occurs very rarely because it involves an energy barrier of about 20 kcal/mol (Cevc and Marsh, 1987). However, lipids are known to be extracted from membranes by various enzymes. One such enzyme is phospholipase A2 (PLA2), which complexes with membrane surfaces, destabilizes a phospholipid, extracts it from the membrane, and catalyzes the hydrolysis reaction of the srir2-acyl chain of the lipid, producing lysophospholipids and fatty acids (Slotboom et al., 1982 Dennis, 1983 Jain et al., 1995). SMD simulations were employed to investigate the extraction of a lipid molecule from a DLPE monolayer by human synovial PLA2 (see Eig. 6b), and to compare this process to the extraction of a lipid from a lipid monolayer into the aqueous phase (Stepaniants et al., 1997). 

When this equation is applied to a system composed of a macromolecule immersed in an aqueous medium containing a dissolved electrolyte, the fixed partial charges of each atom of the macromolecule result in a charge density described by p, and the mobile charges of the dissolved electrolyte are described by /O , which i derived from a Boltzmann distribution of the ions and coions. 

Chambers C C, G D Hawkins, C J Cramer and D G Tmlilar 1996. Model for Aqueous Solvation Ba sed on Class IC Atomic Charges and First Solvation Shell Effects. Journal of Physical Chemistry 100 16385-16398. 

Sodium me/aperiodate (NalO ) in cold aqueous solution readily oxidises 1,2-diols with splitting of the molecule and the consequent formation of aldehydes or ketones thus ethylene glycol gives formaldehyde and pinacol gives acetone. In the case of a 1,2,3-triol, the central carbon atom of the triol... 

The conversion of a carbonyl compound by ammonium polysulphide solution into an amide with the same number of carbon atoms is known as the Willgerodt reaction. The procedure has been improved by the addition of about 40 per cent, of dioxan or of pyridine to increase the mutual solubility of the ketone and aqueous ammonium polysulphide the requisite temperature is lowered to about and the yield is generally better. 

Aromatic aldehydes, and also aliphatic aldehydes containing no a-hydrogen atom, undergo the Cannizzaro reaction (see Section IV,123) when treated with aqueous alkali, for example ... 

In 1965, the Dubna workers found a longer-lived lawrencium isotope, 256Lr, with a half-life of 35 s. In 1968, Thiorso and associates at Berkeley used a few atoms of this isotope to study the oxidation behavior of lawrencium. Using solvent extraction techniques and working very rapidly, they extracted lawrencium ions from a buffered aqueous solution into an organic solvent — completing each extraction in about 30 s. 

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