Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ion special

NITRATIONS WITH NITRONIUM IONS SPECIAL CASES... [Pg.114]

Sutton LE, Jenkin DG, Mitchell AD, Cross LC, editors. Tables of interatomic distances and configuration in molecules and ions. Special Publ No. 11. London The Chemical Society, 1958. [Pg.43]

Because the inner mitochondrial membrane is impermeable to protons and other ions, special exchange transporters span the membrane to allow passage of ions such as OH, Pf, ATP , ADP, and metabo-htes, without discharging the electrochemical gradient across the membrane. [Pg.101]

Of all the metals in the Periodic Table, lanthanide-based coolants are amongst the most suitable as replacements for helium systems as they can operate best in the low-temperature regime. We now describe some theoretical ideas showing how any paramagnet is able to act as a refrigerant, what makes lanthanide(III) ions special for this application and also a brief summary of current technologies. [Pg.294]

Many studies have been carried out on this reaction. Some of the unusual features of this reaction will be described in Chapter 20. Note that in writing the formulas for linkage isomers, it is customary to write the ligand with the atom that functions as the electron pair donor closest to the metal ion. Special consideration will be given in Chapter 20 to the behavior of cyanide complexes because CN-is also an ambidentate ligand. [Pg.590]

Tables of Interatomic Distances and Configurations in Molecules and Ions. Special Pub. 18, Chem. Soc. (London), Oxford Press 1965... Tables of Interatomic Distances and Configurations in Molecules and Ions. Special Pub. 18, Chem. Soc. (London), Oxford Press 1965...
P. C. Burgers and J. K. Terlouw, Structures and Reactions of Gas-phase Organic Ions, Special Periodic Report, Vol. 10, Royal Society of Chemistry, 1989, p. 35. [Pg.292]

Figure 1 shows that photoirradiation of the samples pretreated at 350°, 450°, 550° C causes an increase in intensity of the 540-600-nm H+M-M+ band. This indicates the formation of additional M+ cation radicals under these conditions. The slight increase in intensity of the 540-600-nm band for the sample treated at 550° C, compared with the samples treated at 350° and 450° C, is apparently limited by the number of proton-donating sites and MH+ ions associated with it. The absence of H+M-M+ after M+ cation radicals are formed (sample treated at 750° C) can be caused by the complete absence of proton-donating sites and consequently by the impossibility of forming MH+ ions. Special attention should be paid to the effects caused by photoirradiation of the samples heat treated at 200° and 650°C. The appearance of H+M-M+ in the first case can be explained by assuming that the photoirradiation itself produces some M+ cation radicals from excess of MH+ ions. In the second case excess M+ cation radicals are observed on photoirradiation. The 540-600-nm band was observed after treatment at 650° C in type Y zeolites only (see Table I). [Pg.248]

Molecules and Ions, (Special Publication No. 11), The Chemical Society, London, 1958. [Pg.117]

Magnetic dipole transitions play a role in the luminescence of some lanthanide ions, specially Eu +, when the local symmetry deviates little from inversion symmetry. They are parity-allowed between states ofthe3d or4f configurations but have a low probability. They are subject to selection rules AL = A5" = 0 and AJ = 0, 1 (0 0 forbidden). [Pg.2401]

Besides the use of half-cells involving metal ions, special reference must be made to electrodes capable of measuring [H+] and especially to the modem glass electrode. pH-metry is the most powerful method for the determination of stabihty constants - indeed, 90% or more of stability constant data have been obtained by this method. Values of [H+] are readily obtained by a precalibration method. ... [Pg.4549]

The molecular constants, bond distance, and bond angle were determined by electron diffraction by Pinbak et al. (2, ). The constants reported by Pinbak et al. (3 ) in 1943 were selected. These constants are listed in "Tables of Interatomic Distances and Configuration in Molecules and Ions," Special Publication No. 11, The Chemical Society (London), 1958. The principal moments of inertia calculated from these constants are B C " 10 g cm. ... [Pg.550]

In addition, excellent treatment of this topic may be found in the books by MuUin (2001) and Mersmann (2001). The major part of this literature is focused on the study of precipitation of inorganic compounds by reactions between ions. Specialized studies of organic compounds are also treated including, for example, ethyicncdiaminctctraacctic acid (EDTA) (Myerson et al. 2001) and calcium oxalate (Marcant and David 1991). [Pg.208]

Table of Interatomic Distance and Configuration in Molecules and Ions. Special Pub. [Pg.241]

The pH electrode may be used to make measurements of the hydrogen ion activity by directly immersing the electrodes in the water flow. In this case, it is not possible to buffer the solution and since the pH measurement is normally made in this way there is no problem for pH measurement. Other ion-selective electrodes tend not to be used in this way as activity measurements are not normally used for other ions. Special cells are required for pH measurements, which are carried out in situ. These are of two types cells for use in pipework where the cell is part of the pipe that carries the water, and dip cells that are used to dip the electrodes into ponds, lakes, reservoirs, and other water supplies. [Pg.2388]

Mn04 ions, specially when dealing with small concentrations of the latter. [Pg.304]

The apparent volume data show that is indeed possible to estimate the position of the CMC based solely on volumetric data. Moreover, compared to other methods (ST, FL, NMR) that are frequently used to estimate CMCs,such analysis also provides some insights concerning the behavior of the solute in the midst of the water molecules. As was mentioned before, the increase in the solutions density is caused by the partial breakup of the hydrogen-bonded network of water molecules due to the intrusion of the solute ions, specially the aliphatic moieties that cause the existence of hydrophobic effects. The small apparent molar volumes of the solutes at the most diluted solutions (around 226cm. mok for [CgCpmJCl solutions below CMC at 298 K (ct Fig. 5.7), as compared to 229cm. moF for pure [CgC imJCl at the same temperature)... [Pg.112]

Theory of outer-sphere electron transfer reactions between ions. Special features of electron tranter between ions... [Pg.267]

In the development of these techniques, it is important to remember that lanthanide ions, specially those doped into solids, have played a leading role initially as laser sources themselves and later as prototypical optical systems on which to carry out and demonstrate laser spectroscopy technique. This is principally because (4f) systems basically have attractive properties which are amenable to such studies. [Pg.474]

Chemical transformations of MCMs in aqueous and polar solvents are accompanied by ionization and dissociation. This also can result in the formation of products devoid of the metal. The degree of dissociation depends both on the nature of solvent and the temperature (Fig. 9). This is especially so in the case of transition metal carboxylates, which are strong electrolytes in water. In aqueous or water-oiganic media at pH > 7, salts of unsaturated carboxylic acids are almost completely dissociated (the molar electrical conductivity at infinite dilution, A, , is 146-154cmOhm mol ) hence instead of MCMs, other species such as acrylate and methacrylate ions (specially, metal acrylates and methacrylates) act as monomers. Similarly, in the acrylonitrile-sodium prop-2-enesulfonate system, which undergoes copolymerization in DMSO-H2O mixtures at various pH values (at 45°C with AIBN as the initiator), the relative reactivities of the comonomers change in different media due to the increase in the solvation capacity of water. Actually, copolymerization in these systems involves three types of monomers CH2=CH CH2SO3 Na... [Pg.175]


See other pages where Ion special is mentioned: [Pg.115]    [Pg.241]    [Pg.42]    [Pg.37]    [Pg.115]    [Pg.283]    [Pg.4]    [Pg.249]    [Pg.42]    [Pg.726]    [Pg.299]    [Pg.7195]    [Pg.298]    [Pg.78]    [Pg.87]   


SEARCH



Nitrations with nitronium ions special cases

Special Considerations in the Use of Ion-Selective Electrodes

Special case of negative ions

Special ion exchange materials

Special possibilities of ion exchange

© 2024 chempedia.info