Gas-Phase Acidities of Some Neutral Brønsted Superacids:  A DFT and ab Initio Study

Abstract

For the first time G2 or G2(MP2) calculations or both have been performed to calculate the acidity and deprotonation enthalpy of classical strong mineral acids HClO4, CF3SO3H, FSO3H, H2SO4, HBF4, HPO3, and HNO3. Also, the intrinsic acidities and gas-phase deprotonation enthalpies for 39 neutral strong or superstrong Brønsted acids, Brønsted−Lewis conjugate acids, and some compounds modeling the acidic clusters of zeolites were calculated using the DFT B3LYP 6-311+G** approach. DFT B3LYP method at 6-31+G* basis was used for the calculation of the intrinsic Brønsted acidities of the conjugate acids of the carborane anion CB11H12 - and its mono-, hexa-, and dodecafluorinated analogues. G2 and G2(MP2) theories describe the acidities of different compounds better than DFT B3LYP//6-311+G**. However, the DFT results could also be used for the estimation of the acidity of compounds which are out of reach of G2 or G2(MP2) theory. The estimated ΔG acid values obtained this way can be used as the substitutes for the unavailable experimental values, especially for those (rather numerous) compounds for which the experimental determination of ΔG acid is very difficult. In the case of practically all considered families of compounds extremely high acidities (low ΔG acid values) could be reached. If the compounds were started from HF as the parent acid, then the estimated ΔG acid as low as 249.0 kcal/mol (for F(OSO2)4H) could be reached by formation of Brønsted−Lewis conjugate acids by consecutive complexation with SO3 molecules. Also very low ΔG acid value (ΔG acid(HSbF6) = 255.5) could be reached by complexation of HF with SbF5. At least as high intrinsic acidities as in case of the strongest Brønsted−Lewis superacids could be reached in the case of progressive introduction of highly electronegative, correctly oriented polarizable dipolar electron-accepting substituents into the acidity site. Indeed, the introduction of five CN groups into cyclopentadiene is expected to lead to the acidity ΔG acid = 250.1 kcal/mol which is lower than the corresponding quantity even for hexafluoroantimonic acid (ΔG acid = 255.5 kcal/mol). However, by far the strongest intrinsic Brønsted acidity (ΔG acid = 209 kcal/mol) for dodecafluorosubstituted carborane acid CB11F12H is predicted to exceed the intrinsic acidity of sulfuric acid by about 90 kcal/mol or by almost 70 powers of ten, whereas semi-empirical PM3 calculations suggest that the conjugate acid of the dodecatrifluoromethylmonocarborane anion CB11(CF3)12 - could be the first neutral Brønsted superacid whose acidity (deprotonation energy) is expected to be below the landmark 200 kcal/mol level. An approximate linear relationship is found to hold between the calculated gas-phase acidities of strong and superstrong Brønsted acids and the corresponding Hammett acidity functions of the corresponding neat acids. The simultaneous existence of the widely overlapping areas on the gas-phase acidity scale of neutral and cationic Brønsted acids evidences strongly for the feasibility of the spontaneo...

Electrochemical Syntheses of Cyclo[n]pyrrole

“…Therefore, for the purposes of comparison, we used the gas-phase acidities of the corresponding conjugate acids, either experimental (HX) or calculated (HNO 3 , H 2 SO 4 , HClO 4 , and HBF 4 ). [37][38][39] By using these values, a . TBA = tetra-n-butylammonium, TPA = tetra-n-propylammonium, TEA = tetraethylammonium.…”

Simple Access to the Non‐Oxidizing Lewis Superacid PhF→Al(ORF)3 (RF=C(CF3)3)

“…[11] This definition may be seen in analogy to Brønsted acids: Brønsted superacids are stronger than the strongest conventional Brønsted acid, 100 % H 2 SO 4 . [12] Analogously, SbF 5 is commonly viewed as the strongest conventional Lewis acid.…”

The Strongest Isolable Acid

“…They sublime under vacuum, or melt at atmospheric pressure, at temperatures well above 150 8C. Gas-phase acidities have been calculated for carborane acids, which rank them the strongest of any known isolable acid, [6] but it is presently not possible to translate gas-phase DG data into measures of condensedphase acidity.…”