Heteronuclear NMR spectroscopy as a surface-selective technique: a unique look at the hydroxyl groups of γ-alumina.

The surface hydroxyl groups of γ-alumina dehydroxylated at 500 °C were studied by a combination of one- and two-dimensional homo- and heteronuclear (1)H and (27)Al NMR spectroscopy at high magnetic field. In particular, by harnessing (1)H-(27) Al dipolar interactions, a high selectivity was achieved in unveiling the topology of the alumina surface. The terminal versus bridging character of the hydroxyl groups observed in the (1)H magic-angle spinning (MAS) NMR spectrum was demonstrated thanks to (1)H-(27) Al RESPDOR (resonance-echo saturation-pulse double-resonance). In a further step the hydroxyl groups were assigned to their aluminium neighbours thanks to a {(1)H}-(27) Al dipolar heteronuclear multiple quantum correlation (D-HMQC), which was used to establish a first coordination map. Then, in combination with (1)H-(1) H double quantum (DQ) MAS, these elements helped to reveal intimate structural features of the surface hydroxyls. Finally, the nature of a peculiar reactive hydroxyl group was demonstrated following this methodology in the case of CO2 reactivity with alumina.