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A partial formation

Chloro-triphenylmethane constitutes a classical example for distinguishing the ionizing and dissociating ability of a solvent. In 1902, Walden used it in liquid sulfur dioxide in the first demonstration of the existence of carbenium ions [147]. The colourless chloro-triphenylmethane dissolves in liquid sulfur dioxide (fir = 15.6 at 0 °C), giving an intense yellow colour (2max = 430 nm). This is caused by a partial formation of ion pairs, which do not conduct electricity. At low concentrations, the ion pairs partially dissociate into free ions, which do conduct electricity [148, 149]. [Pg.49]

In all the preceding structures, the sheets of [R4X] tetrahedra - hexagonal, tetragonal or with lower symmetries - are separated from one another by double layers of the Z anions. The only exception is the Te atoms in the (TbS)2Te structural type, which are in a single layer, with a disordered arrangement and a partial formation of Te2 pairs. [Pg.76]

Oxaloacetate is then decarboxylated into pyruvate in Oenococcus, the most important bacteria in enology. In certain lactobacillus, it can also lead to a partial formation of succinate and formate. Pyruvate is the source of acetoin compounds diacetyl, acetoin and 2,3-butanediol. The first is particularly important organoleptically. It is the very aromatic molecule that gives butter its smell. The olfac-tive intensity of acetoin and butanediol, which are derived from diacetyl by reduction of the ketonic functions, is much lower (Figure 5.6). [Pg.150]

More recent developments are based on the finding, that the d-orbitals of silicon, sulfur, phosphorus and certain transition metals may also stabilize a negative charge on a carbon atom. This is probably caused by a partial transfer of electron density from the carbanion into empty low-energy d-orbitals of the hetero atom ( backbonding ) or by the formation of ylides , in which a positively charged onium centre is adjacent to the carbanion and stabilization occurs by ylene formation. [Pg.6]

The flows of gas and liquid need not be concentric for aerosol formation and, indeed, the two flows could meet at any angle. In the cross-flow nebulizers, the flows of gas and sample solution are approximately at right angles to each other. In the simplest arrangement (Figure 19.11), a vertical capillary tube carries the sample solution. A stream of gas from a second capillary is blown across this vertical tube and creates a partial vacuum, so some sample solution lifts above the top of the capillary. There, the fast-flowing gas stream breaks down the thin film of sample... [Pg.144]

Any discussion based on reactivity ratios is kinetic in origin and therefore reflects the mechanism or, more specifically, the transition state of a reaction The transition state for the addition of a vinyl monomer to a growing radical involves the formation of a partial bond between the two species, with a corre sponding reduction of the double-bond character of the vinyl group in the monomer ... [Pg.436]

Emissions from methanol vehicles are expected to produce lower HC and CO emissions than equivalent gasoline engines. However, methanol combustion produces significant amounts of formaldehyde (qv), a partial oxidation product of methanol. Eormaldehyde is classified as an air toxic and its emissions should be minimized. Eormaldehyde is also very reactive in the atmosphere and contributes to the formation of ozone. Emissions of NO may also pose a problem, especiaHy if the engine mns lean, a regime in which the standard three-way catalyst is not effective for NO reduction. [Pg.195]

A critical component of the G-protein effector cascade is the hydrolysis of GTP by the activated a-subunit (GTPase). This provides not only a component of the amplification process of the G-protein cascade (63) but also serves to provide further measures of dmg efficacy. Additionally, the scheme of Figure 10 indicates that the coupling process also depends on the stoichiometry of receptors and G-proteins. A reduction in receptor number should diminish the efficacy of coupling and thus reduce dmg efficacy. This is seen in Figure 11, which indicates that the abiUty of the muscarinic dmg carbachol [51 -83-2] to inhibit cAMP formation and to stimulate inositol triphosphate, IP, formation yields different dose—response curves, and that after receptor removal by irreversible alkylation, carbachol becomes a partial agonist (68). [Pg.278]

TOCSY Total correlation spectroscopy, in the homonuclear COSY format, e.g. HH TOCSY traces out all proton-proton coimectivities of a partial structure in addition to the coimectivities (V, V, V, J) as detected by HH COSY... [Pg.267]

In 1931 Winterfeld and Kneuer, as a result of their observation that jS-lupinane can be obtained from lupanine, and the formation of 2-methyl-pyrrolidine by the oxidation of sparteine, combined these two features in a partial formula (II) for lupanine, which could be developed in various ways depending on the mode of attachment of the methylpyrrolidine residue. In view, however, of Ing s demonstration of the relationship of anagyrine, CJ5H20ON2, to Z-lupanine, CJ5H24ON2, and d-sparteine, C15H28N2, it was elearly neeessary to consider formul for lupanine derivable from the two alternati-ves, which Ing had proposed for anagyrine and which are shown below as (III) and (IV) with the formul for lupanine derived from them (V) by Ing and (VI) by Clemo and Raper. Sparteine would be represented by (V) or (VI) with the change CO CH2. [Pg.130]

The formation of cotar none from cotar nine methine methiodide by the action of potash (IX—X) led Roser to represent cotarnine and its salts by the following formulae, the loss of a molecule of water in the formation of cotarnine salts being explained by the production of a partially reduced pyridine ring, which is fully hydrogenated in the reduction of cotarnine to hydrocotarnine. In the reverse process, oxidation of liydrocotarnine to cotarnine, Roser assumed the scission of the ring at the point indicated, with the formation of a hydration product, and oxidation of the latter to cotarnine thus —... [Pg.203]

A partial explanation, at least, can be provided for the relative abundances and ease of formation of the above stereochemical varieties of Ni complexes. It can be seen from Table 26.6 that the CFSEs of the d configuration, unlike those of the d configuration (e.g. Co ), favour an... [Pg.1157]

On-off control of steam systems can result in the formation of a partial vacuum, leading to condensate locking... [Pg.411]


See other pages where A partial formation is mentioned: [Pg.445]    [Pg.250]    [Pg.533]    [Pg.601]    [Pg.408]    [Pg.707]    [Pg.233]    [Pg.212]    [Pg.445]    [Pg.250]    [Pg.533]    [Pg.601]    [Pg.408]    [Pg.707]    [Pg.233]    [Pg.212]    [Pg.224]    [Pg.165]    [Pg.216]    [Pg.525]    [Pg.202]    [Pg.4]    [Pg.274]    [Pg.243]    [Pg.165]    [Pg.287]    [Pg.336]    [Pg.534]    [Pg.42]    [Pg.1313]    [Pg.176]    [Pg.248]    [Pg.634]    [Pg.369]    [Pg.259]    [Pg.83]    [Pg.195]    [Pg.216]    [Pg.186]    [Pg.58]    [Pg.180]    [Pg.21]    [Pg.309]    [Pg.1336]    [Pg.576]    [Pg.96]   
See also in sourсe #XX -- [ Pg.14 , Pg.194 ]




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