Lewis Acidic Aluminosilicates: Synthesis, 27Al MQ/MAS NMR, and DFT-Calculated 27Al NMR Parameters

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Publikace nespadá pod Pedagogickou fakultu, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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KEJÍK Martin BRUS Jiri JEREMIAS Lukas ŠIMONÍKOVÁ Lucie MORAVEC Zdeněk KOBERA Libor STÝSKALÍK Aleš BARNES Craig E. PINKAS Jiří

Rok publikování 2024
Druh Článek v odborném periodiku
Časopis / Zdroj Inorganic Chemistry
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://pubs.acs.org/doi/10.1021/acs.inorgchem.3c04035
Doi http://dx.doi.org/10.1021/acs.inorgchem.3c04035
Klíčová slova Aromatic compounds; Condensation; Ligands; Materials; Nuclear magnetic resonance spectroscopy
Popis Porous aluminosilicates are functional materials of paramount importance as Lewis acid catalysts in the synthetic industry, yet the participating aluminum species remain poorly studied. Herein, a series of model aluminosilicate networks containing [L–AlO3] (L = THF, Et3N, pyridine, triethylphosphine oxide (TEPO)) and [AlO4]- centers were prepared through nonhydrolytic sol–gel condensation reactions of the spherosilicate building block (Me3Sn)8Si8O20 with L–AlX3 (X = Cl, Me, Et) and [Me4N] [AlCl4] compounds in THF or toluene. The substoichiometric dosage of the Al precursors ensured complete condensation and uniform incorporation, with the bulky spherosilicate forcing a separation between neighboring aluminum centers. The materials were characterized by 1H, 13C, 27Al, 29Si, and 31P MAS NMR and FTIR spectroscopies, ICP-OES, gravimetry, and N2 adsorption porosimetry. The resulting aluminum centers were resolved by 27Al TQ/MAS NMR techniques and assigned based on their spectroscopic parameters obtained by peak fitting (?iso, CQ, ?) and their correspondence to the values calculated on model structures by DFT methods. A clear correlation between the decrease in the symmetry of the Al centers and the increase of the observed CQ was established with values spanning from 4.4 MHz for distorted [AlO4]- to 15.1 MHz for [THF–AlO3]. Products containing exclusively [TEPO–AlO3] or [AlO4]- centers could be obtained (single-site materials). For L = THF, Et3N, and pyridine, the [AlO4]- centers were formed together with the expected [L–AlO3] species, and a viable mechanism for the unexpected emergence of [AlO4]- was proposed.
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