332-11-6Relevant academic research and scientific papers
Electrophilic Aromatic Substitution. Charge-Transfer Excited States and the Nature of the Activated Complex
Fukuzumi, S.,Kochi, J. K.
, p. 7240 - 7252 (2007/10/02)
Transient charge-transfer (CT) absorption bands are observed for various benzene derivatives interacting with typical electrophiles, such as the halogens and mercuric trifluoroacetate.The second-order rate constants k for the kinetics of the disappearance of these spectral bands coincide with the rate constants for electrophilic halogenation and mercuration of the aromatic ring.The relative reactivities (log k/k0) of the arenes in electrophilic aromatic substitution are linearly related to the reactive CT transition energies ΔhνCT, using benzene as the reference arene.This remarkable correlation thus relates the transition state for electrophilic aromatic substitution to the CT excited state +E->* of the arene-electrophile pair.Such a direct relationship requires that the solvation energies remain constant for various aromatic cations, since the transition state is attained by an adiabatic process whereas the CT excitation involves a vertical (Franck-Condon) process.Indeed, independent measurements of the cyclic voltammetric peak potentials in acetonitrile and trifluoroacetic acid in comparison with tha gas-phase ionization potentials support the constancy of the solvation terms.The latter provides a ready explanation for the previously puzzling observations that the relative reactivities log k/k0 are insensitive to solvent polarity, yet the absolute rates of electrophilc aromatic substitution are highly dependent.The CT formulation for electrophilic aromatic substitution also provides a physical interpretation of the linear free energy relationship (LFER) which has been established between the ?+ substituent constants and the relative reactivities of arenes.The slope of the LFER correlation ρ is shown to be a measure of the mean separation in the transition state.Other LFER's found between electrophilic aromatic substitution and such parameters as the proton affinities and the ? and the ? basisities of arenes are similarly interpreted.The prediction of the isomeric product distribution resulting from electron-releasing X and electron-withdrawing Y substituents is an important, natural consequence of the CT formulation.It provides unusual insight into the transition from the electron-poor arenes (Ph-Y) producing predominantly meta-substituted products to those (Ph-X) affording the para isomers.
Kinetics and Mechanism of Mercuriation of Aromatic Compounds by Mercury Trifluoroacetate in Trifluoroacetic Acid
Fung, Chung W.,Khorramdel-Vahed, Mehdi,Ranson, Richard J.,Roberts, Roger M. G.
, p. 267 - 272 (2007/10/02)
The mercuriation of a series of aromatic derivatives by mercury(II) trifluoroacetate in trifluoroacetic acid has been studied using titrimetric and spectrophotometric methods.The latter method has revealed the presence of a rapidly formed ?-complex intermediate and values of the thermodynamic parameters of its formation have been computed.Only small kinetic isotope effects were found for the complex-forming step in contrast to the large values obtained for the slow step.The effect of added salts was investigated and the mechanism of the reaction discussed in detail in the light of these results.Mercuriation by a readily synthesised mixed acetate, Hg(OCOCF3)-(OCOCH3), is also reported as well as some preliminary studies of triptycene derivatives.
