Abstract
13C and 1H spectra have been determined for 18 4-substituted phenylacetylenes and carbon charge densities have been estimated by CNDO/2 molecular orbital calculations. Correlations of these parameters with σ1, and σR0 indicate that the important mechanisms of transmission of substituent effects are field, resonance, and π polarization effects, as previously noted for 4-substituted styrenes. Evidence is presented that demonstrates that both 1H and 13C chemical shifts for these compounds reflect ground state charge densities. CNDO/2 calculations on a variety of aromatic derivatives suggest that the σ1, dependence of 19F chemical shifts in these derivatives may primarily be due to π polarization.

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