Electron-donating ability

Decreasing the electron donating ability of an ammo group by acylation makes it possi ble to limit halogenation to monosubstitution... 

The relative electron-donating ability of rings can be estimated by the change in the infrared stretching frequencies of attached amino, carbonyl, cyano, or methoxy groups, but the quantitative relation to chemical reactivity does not appear to be defined at... 

Ethylbenzene and toluene are hydrogenated faster than benzene over Cu-ZnO, contrary to the general rule. Such behavior is evidence for a t bonded intermediate, the surface concentration of which increases with the increasing electron-donating ability of the system (5(5). 

The Pt—P (and Pt—Cl) bond lengths correlate with the electron-donating ability of the phosphine (Tolman s Xi factor) rather than steric factors (the cone angle of the tertiary phosphine) [150b]. 

In Eq. (10-17), parameters a and b measure the sensitivity of the reaction to these nucleophilic parameters. Since H measures proton basicity and En the electron-donation ability, this treatment models nucleophilicity as a combination of electron loss and electron pair donation. The Edwards equation is thus an oxibase scale of nucleophilic reactivity. Table 10-5 summarizes the nucleophilic parameters. 

Scheme 10 Suppression of the CO insertion by the electron-donating ability of a dialkyamino moiety [54-56]...

Basicity, concept of, 71 as electron-donating ability of terminal groups, 68... 

This chapter is restricted to a discussion of halogen-bonded complexes B XY that involve a homo- or hetero-dihalogen molecule XY as the electron acceptor and one of a series of simple Lewis bases B, which are chosen for their simplicity and to provide a range of electron-donating abilities. Moreover, we shall restrict attention to the gas phase so that the experimental properties determined refer to the isolated complex. Comparisons with the results of electronic structure calculations are then appropriate. All of the experimental properties of isolated complexes B- XY considered here result from interpreting spectroscopic constants obtained by analysis of rotational spectra. 

The intermediate N-acylpyridinium salt is highly stabilized by the electron donating ability of the dimethylamino group. The increased stability of the N-acylpyridinium ion has been postulated to lead to increased separation of the ion pair resulting in an easier attack by the nucleophile with general base catalysis provided by the loosely bound carboxylate anion. Dialkylamino-pyridines have been shown to be excellent catalysts for acylation (of amines, alcohols, phenols, enolates), tritylation, silylation, lactonization, phosphonylation, and carbomylation and as transfer agents of cyano, arylsulfonyl, and arylsulfinyl groups (lj-3 ). 

Allenyl cations 1 are a stabilized form of vinyl cations1-3 in which the /1-carbon atom of the vinylic structure is part of the substituent which effects the stabilization of the ion via its electron-donating ability. This leads to a resonance hybrid having formally the alkynyl cation structure 2. Allenyl cations should be distinguished from the allenyl substituted carbenium ions 3 formulated as the mesomeric structures of the vinyl cations 4 (dienyl cations) stabilized by an w-vinyl group (equation 1). 

With increasing n electron-donating ability of the substituents, A Hr decreases. This reflects primarily the increased stability of the carbene, and is... 

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