Driving the Active Site Incorporation in Zeolitic Materials via the Organic Structure‐Directing Agent Through Development of H‐Bonds with Hydroxyl Groups
(1S,2S)‐N‐methyl‐pseudoephedrine (MPS) was used as organic structure‐directing agent (OSDA) for the synthesis of Mg‐doped nanoporous aluminophosphates. This molecule displays a particular conformational behavior, where the presence of H‐bond donor and acceptor groups provide a rigid conformational s...
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Published in | Chemistry : a European journal Vol. 28; no. 42; pp. e202200702 - n/a |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
26.07.2022
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | (1S,2S)‐N‐methyl‐pseudoephedrine (MPS) was used as organic structure‐directing agent (OSDA) for the synthesis of Mg‐doped nanoporous aluminophosphates. This molecule displays a particular conformational behavior, where the presence of H‐bond donor and acceptor groups provide a rigid conformational space with one asymmetric conformation preferentially occurring. MPS drives the crystallization of Mg‐containing AFI materials. Characterization of these materials shows that the OSDA incorporate as protonated species, arranged as head‐to‐tail monomers. Combination of three‐dimensional electron diffraction with high‐resolution synchrotron powder X‐ray diffraction allowed to locate both the Mg and the organic species. Interestingly, results showed that the spatial incorporation of Mg is driven by the hydroxyl groups of the organic cation through the development of H‐bonds with negatively‐charged MgO4 tetrahedra. This work demonstrates that H‐bond forming groups can be used to drive the spatial incorporation of low‐valent dopants within zeolitic frameworks, a highly desired aim in order to control their catalytic activity and selectivity.
(1S,2S)‐N‐methyl‐pseudoephedrine used as organic structure‐directing agent for the synthesis of Mg‐doped aluminophosphates is able to control the spatial distribution of low‐valent dopants through the development of H‐bonds with MgO4 tetrahedra, providing a new strategy for controlling the active site spatial distribution in zeolite catalysts. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0947-6539 1521-3765 1521-3765 |
DOI: | 10.1002/chem.202200702 |