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Título

Effect of fluorine and molecular charge-state on the aggregation behavior of (S)-(-)-N-benzylpyrrolidine-2-methanol confined within the AFI nanoporous structure

AutorGómez-Hortigüela Sainz, Luis CSIC ORCID ; López-Arbeloa, Fernando; Márquez Álvarez, Carlos CSIC ORCID ; Pérez-Pariente, Joaquín CSIC ORCID
Fecha de publicación2013
EditorAmerican Chemical Society
CitaciónJournal of Physical Chemistry C 117(17): 8832-8839 (2013)
ResumenThe effect of the molecular charge-state and of the presence of fluorine atoms on the aggregation behavior of (S)-(-)-N-pyrrolidine-2-methanol has been studied by fluorescence and FTIR spectroscopies in aqueous solution and when confined within the nanoporous AFI structure during crystallization or after gas-phase adsorption. Results show that a higher aggregation is achieved via inclusion of the guest molecules in postsynthetic gas-phase adsorption treatments compared to what occurs during crystallization. In the former case, neutral species are incorporated within the aluminophosphate AFI framework, as evidenced by FTIR, which results in a high aggregation because of the lack of electrostatic repulsions. In contrast, a lower aggregation is observed when the organics are occluded during crystallization, which in turn is dependent on the presence of heteroatoms. In the undoped aluminophosphate systems, FTIR results show that the molecules are incorporated mainly as neutral species, which leads to a higher aggregation. On the contrary, on Mg- and Zn-doped systems, FTIR shows that the molecules are protonated; interestingly, this results in a lower aggregation on Mg-doped systems. However, a higher aggregation is observed for Zn-doped systems despite the charged molecular state, suggesting that the chemical nature of the dopant does influence the aggregation behavior. Fluorine in ortho- or meta-positions of the aromatic ring leads to a partial deaggregation of the molecules in solution and within the nanoporous structures, leading to a preferential incorporation of monomers within the AFI framework. This is probably due to an inductive effect caused by fluorine, which withdraws electron density from the aromatic ring, this being the driving-force for this type of aggregation. © 2013 American Chemical Society.
Versión del editorhttps://doi.org/10.1021/jp401135f
URIhttp://hdl.handle.net/10261/181681
DOI10.1021/jp401135f
ISSN1932-7447
E-ISSN1932-7455
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