Brønsted acid sites (BAS) in dry aluminosilicate zeolites, also known as bridging O H −H groups, may form hydrogen bonds with other framework oxygen atoms, O, in addition to BAS that are free of such interactions. These are referred to as perturbed and unperturbed BAS, respectively. However, hydrogen bonding may occur only for specific geometric orientations between two framework oxygen atoms, allowing an O H −H•••O interaction. To evaluate the possibility for such hydrogen bonding, we introduce an alignment angle κ that describes the angle between the Si−O H −Al bisector and the O H −O direction of a potential hydrogen-bonding donor−acceptor pair. A total of 27 zeolite framework topologies were analyzed, and the relevance of this approach was subsequently demonstrated for H-ZSM-5 with two different Si/Al ratios. Here, it could be unequivocally shown by advanced solid-state NMR methods that the debated 1 H NMR signal at ∼6 ppm arises due to the formation of hydrogen-bonded BAS.

The effect of outer-sphere environment on alkene epoxidation catalysis using an organic hydroperoxide oxidant is demonstrated for calix[4]arene-Ti single-sites grafted on amorphous vs crystalline delaminated zeotype (UCB-4) silicates as supports. A chelating calix[4]arene macrocyclic ligand helps enforce a constant Ti inner-sphere, as characterized by UV-visible and X-ray absorption spectroscopies, thus enabling the rigorous comparison of outer-sphere environments across different siliceous supports. These outer-sphere environments are characterized by solid-state H NMR spectroscopy to comprise proximally organized silanols confined within 12 membered-ring cups in crystalline UCB-4, and are responsible for up to 5-fold enhancements in rates of epoxidation by Ti centers.

Among some few others tests, the evaluation of the Atterberg limits is a very basic soil mechanical test allowing a first insight into the chemical reactivity of clays. Basically, the liquid limit and the plasticity index are highly and mainly influenced by the ability of clay minerals to interact with liquids. In this contribution, a correlation between the Atterberg limits and clay mineralogy is proposed. This correlation increases the understanding between clay mineralogists and engineers in soil mechanics; additionally a wealth of information in clay mineralogy literature is now available to predict the mechanical behaviour of clays via index tests. D

Nests of three silanol groups are located on the internal pore surface of calcined zeolite SSZ‐70. 2D 1H double/triple‐quantum single‐quantum correlation NMR experiments enable a rigorous identification of these silanol triad nests. They reveal a close proximity to the structure directing agent (SDA), that is, N,N′‐diisobutyl imidazolium cations, in the as‐synthesized material, in which the defects are negatively charged (silanol dyad plus one charged SiO− siloxy group) for charge balance. It is inferred that ring strain prevents the condensation of silanol groups upon calcination and removal of the SDA to avoid energetically unfavorable three‐rings. In contrast, tetrad nests, created by boron extraction from B‐SSZ‐70 at various other locations, are not stable and silanol condensation occurs. Infrared spectroscopic investigations of adsorbed pyridine indicate an enhanced acidity of the silanol triads, suggesting important implications in catalysis.

Two pairs of Brønsted acid sites have been identified in H,Na-Y zeolite, located in the supercage and in the sodalite cage, which upon ultrastabilization (dealumination) are transformed into pairs of Brønsted and Lewis acid sites. This mild postsynthetic modification step is an important process for converting this material into an active catalyst for large-scale commercial reactions. Pairing structures and their transformations have been investigated using H double-quantum NMR spectroscopy experiments for dehydrated zeolite, H,Na-Y, and its ultrastabilized form, H,Na-USY. This approach enables the detection of pairs of Brønsted and Lewis acid sites with unprecedented H resolution and distinguishing them from isolated acid sites. The dealumination is also detected by static Al solid-state NMR experiments.