A Stable Silanol Triad in The Zeolite Catalyst SSZ‐70

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, where 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.