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Ring ionizations

Their antioxidant potential caused by the ability to turn into stable radicals after scavenging deleterious ones is determined by the number and position of free hydroxyl groups. Catechol arrangement at B ring also enhances their ability to chelate metal ions [127]. However, it depends on factors such as pH and reactive species [128] at moderate pH, they can chelate metal ions with B ring ionized hydroxyl groups [129]. [Pg.285]

The best-known equation of the type mentioned is, of course, Hammett s equation. It correlates, with considerable precision, rate and equilibrium constants for a large number of reactions occurring in the side chains of m- and p-substituted aromatic compounds, but fails badly for electrophilic substitution into the aromatic ring (except at wi-positions) and for certain reactions in side chains in which there is considerable mesomeric interaction between the side chain and the ring during the course of reaction. This failure arises because Hammett s original model reaction (the ionization of substituted benzoic acids) does not take account of the direct resonance interactions between a substituent and the site of reaction. This sort of interaction in the electrophilic substitutions of anisole is depicted in the following resonance structures, which show the transition state to be stabilized by direct resonance with the substituent ... [Pg.137]

Step 2 A proton is lost from the sp hybridized carbon of the intermediate to restore the aromaticity of the ring The species shown that abstracts the proton is a hydrogen sulfate ion formed by ionization of sulfunc acid... [Pg.479]

Unlike the case of benzene in which ionization involves loss of a tt electron from the ring electron impact induced ionization of chlorobenzene involves loss of an elec tron from an unshared pair of chlorine The molecular ion then fragments by carbon-chlorine bond cleavage... [Pg.570]

Ring closure of o-benzoylbenzoic acid to anthraquinone is an unusual reaction in that normally it is not predicted to occur ortho to a keto group. Several theories have been proposed to explain the mechanism whereby this could possibly occur. One involves a complex ionization of o-benzoylbenzoic acid (41), the other favors the intermediate formation of 3-hydroxy-3-phenyl-l(3JT)isobenzofuranone (9) [64693-03-4] and 3-phenylphthaHdyl sulfate (10) (42) ... [Pg.423]

Several compounds such as BaZrS [12026-44-7], SrZrS [12143-75-8], and CaZrS [59087-48-8], have been made by reacting carbon disulfide with the corresponding zirconate at high temperature (141), whereas PbZrS [12510-11-1] was produced from the elements zirconium and sulfur plus lead sulfide sealed in a platinum capsule which was then pressurized and heated (142). Lithium zirconium disulfide [55964-34-6], LiZrS2, was also synthesized. Zirconium disulfide forms organometaUic intercalations with a series of low ionization (<6.2 eV)-sandwich compounds with parallel rings (143). [Pg.434]

Another important factor affecting the electronic properties is the steric barrier to planarity along the polymer chain. Since polyheterocycles and polyarylenes must adopt a planar geometry in the ionized state to form quinoid-like segments, steric factors that limit the ability of the polymer to adopt geometries which are planar with respect to adjacent rings have a detrimental effect on the electronic properties (181). [Pg.42]

Alternative ( soft ) ionization techniques are not usually required for aromatic isothiazoles because of the stability of the molecular ions under electron impact. This is not the case for the fully saturated ring systems, which fragment readily. The sultam (25) has no significant molecular ion under electron impact conditions, but using field desorption techniques the M + lY ion. is the base peak (73X3861) and enables the molecular weight to be confirmed. [Pg.143]

Four-membered heterocycles prefer to cleave, upon ionization, into two fragments, each containing two of the ring atoms. Further cleavages commence from these initial fragments (Scheme 5). Specific details can be found as follows azetidines (B-71MS296), oxetanes... [Pg.11]


See other pages where Ring ionizations is mentioned: [Pg.7]    [Pg.4]    [Pg.135]    [Pg.135]    [Pg.274]    [Pg.47]    [Pg.712]    [Pg.7]    [Pg.4]    [Pg.135]    [Pg.135]    [Pg.274]    [Pg.47]    [Pg.712]    [Pg.2070]    [Pg.181]    [Pg.51]    [Pg.975]    [Pg.150]    [Pg.67]    [Pg.319]    [Pg.296]    [Pg.309]    [Pg.468]    [Pg.47]    [Pg.156]    [Pg.427]    [Pg.226]    [Pg.476]    [Pg.477]    [Pg.4]    [Pg.25]    [Pg.60]    [Pg.265]    [Pg.24]    [Pg.25]    [Pg.26]    [Pg.11]    [Pg.69]    [Pg.525]    [Pg.606]    [Pg.774]    [Pg.781]    [Pg.873]    [Pg.46]    [Pg.554]   
See also in sourсe #XX -- [ Pg.274 ]




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Ionization from ring position

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