Stabilization of carbocations CH, CH, i-CH, tert-Bu, and cyclo-pentyl in solid phases: experimental data versus calculations.

Comparison of experimental infrared (IR) spectra of the simplest carbocations (with the weakest carborane counterions in terms of basicity, CHBHal, Hal = F, Cl) with their calculated IR spectra revealed that they are completely inconsistent, as previously reported for the t-Bu cation [Stoyanov E. S., et al. J. Phys. Chem. A, 2015, 119, 8619]. This means that the generally accepted explanation of hyperconjugative stabilization of the carbocations should be revised. According to the theory, one CH bond (denoted as ) from each CH/CH group transfers its σ-electron density to the empty 2p orbital of the sp C atom, whereas the σ-electron density on the other CH bonds of the CH/CH group slightly increases. From experimental IR spectra it follows that donation of the σ-electrons from the bond to the 2p C-orbital is accompanied by equal withdrawal of the electron density from other CH bonds, that is, the electrons are supplied from each CH bond of the CH/CH group. As a result, all CH stretches of the group are red shifted, and IR spectra show typical CH/CH group vibrations. Experimental findings provided another clue to the electron distribution in the hydrocarbon cations and showed that the standard computational techniques do not allow researchers to explain a number of recently established features of the molecular state of hydrocarbon cations.