Journal Article
Science, vol. 372, iss. 6545, pp. 952-957, 2021
Authors
Niklas Pfriem, Peter H. Hintermeier, Sebastian Eckstein, Sungmin Kim, Qiang Liu, Hui Shi, Lara Milakovic, Yuanshuai Liu, Gary L. Haller, Eszter Baráth, Yue Liu, Johannes A. Lercher
Abstract
Speeding reactions through ionic strength
Brønsted acidity is introduced into microporous zeolites through the addition of framework aluminum. Pfriem
et al.
show that in the presence of water, the limited volume in the microchannels of zeolite H-MFI leads to a high concentration of hydrated hydronium ions at aluminum sites. The resulting high charge density creates a highly non-ideal solvation environment and, for cyclohexanol dehydrogenation, the charged carbenium-ion transition state was stabilized. A higher rate was maintained with lower-acidity sodium ion–exchanged zeolites that had the same high ionic strength.
Science
, abh3418, this issue p.
952