Electronegativity constants

The aromaticity electronegativity constants for the case R = H are indicated in parentheses (80PAC1409 85MI2). 

Secondly he shifted his electronegativity scale by addition of a constant so that Xh was increased from 0 to 2.1. Drawing on a larger body of thermochemical data [48], he was able to present a table of electronegativity constants for H and 13 other elements, those listed on the previous page plus Si, Ge, P, As, S, and Se. The... 

Since the dissociation energies of many metal atom dimers M2 were unknown, Pauling adopted a less rigorous approach in order to determine the electronegativity constants of metals. Consider the energy of formation of a gaseous metal halide Ml from the gaseous reactants ... 

The correction term in Eq. (9) shows that the basic assumption of additivity of the fragmental constants obviously does not hold true here. Correction has to be appHed, e.g., for structural features such as resonance interactions, condensation in aromatics or even hydrogen atoms bound to electronegative groups. Astonishingly, the correction applied for each feature is always a multiple of the constant Cu, which is therefore often called the magic constant . For example, the correction for a resonance interaction is +2 Cj, or per triple bond it is -1 A detailed treatment of the Ef system approach is given by Mannhold and Rekker [5]. 

Typical coupling constants for isothiazoles are given in Table 5. The electronegative nitrogen atom reduces 3,4 and V3.5 from the values of 3.50 Hz and 0.27 Hz, respectively, in thiophene. The V values correlate quite well with rr-bond orders calculated by MO methods (74CJC833). 

Later methods, especially that of Gordy (1955), and later Allred and Rochow (1958) make use of screening constants of the electron strucmre for the nuclear charge of each atom. This determines die attraction between the nucleus of the atom and an electron outside the normal electron complement, and is die effective nuclear charge. The empirical equation for the values of electronegativity obtained in this manner by Allred and Rochow is... 

Table 2.6. Structural features (carbon hybridisation, electronegativity, ring size) and typical one-bond CH coupling constants Jch (Hz) ...

Substituent effects (electronegativity, configuration) influence these coupling constants in four-, five- and seven-membered ring systems, sometimes reversing the cis-tmns relationship so that other NMR methods of structure elucidation, e.g. NOE difference spectra (see Section 2.3.5), are needed to provide conclusive results. However, the coupling constants of vicinal protons in cyclohexane and its heterocyclic analogues (pyranoses, piperidines) and also in alkenes (Table 2.10) are particularly informative. 

In general, the dissection of substituertt effects need not be limited to resonance and polar components, vdiich are of special prominence in reactions of aromatic compounds.. ny type of substituent interaction with a reaction center could be characterized by a substituent constant characteristic of the particular type of interaction and a reaction parameter indicating the sensitivity of the reaction series to that particular type of interactioa For example, it has been suggested that electronegativity and polarizability can be treated as substituent effects separate from polar and resonance effects. This gives rise to the equation... 

The exceptions are formaldehyde, which is nearly completely hydrated in aqueous solution, and aldehydes and ketones with highly electronegative substituents, such as trichloroacetaldehyde and hexafluoroacetone. The data given in Table 8.1 illustrate that the equilibrium constant for hydration decreases with increasing alkyl substitution. 

---