Beschreibung:
<jats:title>Abstract</jats:title><jats:p>Surface functionalization of porous materials with sulfonic acid (SO<jats:sub>3</jats:sub>H) groups is of particular interest in applications involving ion exchange, acidic catalysis and proton conduction. Macro-mesoporous silica monoliths are ideal support structures for these applications, as they combine advection-dominated mass transport in the macropores with short diffusion lengths and a large surface area (available for functionalization) in their mesoporous skeleton. Here, we report on SO<jats:sub>3</jats:sub>H functionalized sol–gel silica monoliths with bimodal pore systems exhibiting macro- and mesoporosity, prepared according to a simple, efficient in situ synthesis protocol. Based on the co-condensation approach, thiol groups were introduced homogeneously into the pore structure, followed by their oxidation to SO<jats:sub>3</jats:sub>H groups and the simultaneous removal of the template. The macropore size, specific surface area, and coverage with SO<jats:sub>3</jats:sub>H groups are easily adjusted in this synthesis route. Importantly, the hybrid monoliths have a substantially narrower mesopore size distribution (relative standard deviation ~25%) than conventional sol–gel materials (>40%) and can be engineered crack-free in a robust column design (suitable for high-pressure flow-through operation) with mean mesopore size down to ~7 nm. They are characterized by IR spectroscopy, thermogravimetry, and elemental analysis as well as <jats:sup>13</jats:sup>C and <jats:sup>29</jats:sup>Si solid state NMR to corroborate the simple, efficient combination of sol–gel-based material synthesis, surface functionalization, and template removal (i.e., polymer extraction). Complementary, inverse gas chromatography is presented as a new approach to characterize the incorporated SO<jats:sub>3</jats:sub>H groups via surface energy analysis and particularly resolve changes in the Lewis acid–base characteristics engendered by that functionalization.</jats:p>