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BF3 affinity

Basicity in the gas phase is measured by the proton affinity (PA) of the electron donor and in solution by the pAj,. A solution basicity scale for aldehydes and ketones based on hydrogen bond acceptor ability has also been established [186]. Nucleophilicity could be measured in a similar manner, in the gas phase by the affinity for a particular Lewis acid (e.g., BF3) and in solution by the equilibrium constant for the complexation reaction. In Table 8.1 are collected the available data for a number of oxygen systems. It is clear from the data in Table 8.1 that the basicities of ethers and carbonyl compounds, as measured by PA and p , are similar. However, the nucleophilicity, as measured by the BF3 affinity, of ethers is greater than that of carbonyl compounds, the latter values being depressed by steric interactions. [Pg.123]

TABLE 8.1. Ionization Potentials (IP), Proton Affinities (PA), pX), Values, anti BF3 Affinities... [Pg.123]


See other pages where BF3 affinity is mentioned: [Pg.358]    [Pg.359]    [Pg.359]    [Pg.359]    [Pg.361]    [Pg.362]    [Pg.365]    [Pg.366]    [Pg.123]    [Pg.325]    [Pg.325]    [Pg.325]    [Pg.327]    [Pg.328]    [Pg.332]    [Pg.333]    [Pg.336]    [Pg.336]   


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Acetaldehyde BF3 affinity

Acetone BF3 affinity

BF3

BF3 affinity butenone

BF3 affinity dimethyl ether

BF3 affinity formaldehyde

BF3 affinity methanol

BF3 affinity methyl acetate

BF3 affinity methyl acrylate

BF3 affinity nucleophilicity

BF3 affinity oxetane

BF3 affinity table

BF3 affinity tetrahydrofuran

BF3 affinity water

Computation of the BF3 Affinity

Definition of the BF3 Affinity Scale

Introduction Measuring Relative BF3 Affinity by Ligand Exchange in Solution

The BF3 Affinity Scale

The BF3 Affinity Scale Data

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