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Synthesis of a germanosilicate zeolite HPM-12 using a short imidazolium-based dication: Structure-direction by charge-to-charge distance matching

Authors :
Peng Lu
Luis Gómez-Hortigüela
Zihao Gao
Miguel A. Camblor
Ministerio de Economía y Competitividad (España)
Consejo Superior de Investigaciones Científicas (España)
European Commission
Agencia Estatal de Investigación (España)
Lu, Peng [0000-0002-9773-3993]
Gómez-Hortigüela Sainz, Luis [0000-0002-4960-8709]
Gao, Yi [0000-0003-0331-3515]
Camblor, Miguel Ángel [0000-0001-9591-3432]
Lu, Peng
Gómez-Hortigüela Sainz, Luis
Gao, Yi
Camblor, Miguel Ángel
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2019
Publisher :
Royal Society of Chemistry (UK), 2019.

Abstract

[EN] A short imidazolium based dication, with only three methylene units in the spacer linker, selectively directs the crystallization of zeolite HPM-12 (?UOE) as long as there is enough germanium present in the synthesis gel. The integrity of the dication is proved by dissolution of the zeolite and H and C NMR spectroscopy, where significant effects of organic dication concentration and the presence and concentration of HF need to be taken into account. For the as-made HPM-12 zeolite, a large shift of 9 ppm of one resonance in the C MAS NMR spectrum is due to the particular conformation of the dication imposed by confinement in the zeolite framework, as found by DFT calculations. The structure-directing ability of this kind of dication with varying length of the linker suggests that matching of the distance between positive charges (imidazolium moieties) and negative charges (double four rings in which fluoride resides) plays a crucial role during crystallization.<br />The authors acknowledge financial support from the Spanish Ministerio de Economía y Competitividad, the Spanish Agencia Estatal de Investigación and the EU's Fondo Europeo de Desarrollo Regional under projects MAT2016-77496-R (AEI/FEDER, UE) and MAT2015-71117-R (MINECO/FEDER, UE). We acknowledge the support of the publication fee by the CSIC Open Access Publication Support Initiative through its Unit of Information Resources for Research (URICI). P.L. is grateful to the China Scholarship Council (CSC) for a fellowship and to the Dalian Institute of Chemical Physics for permission to leave. Centro Técnico Informático-CSIC is acknowledged for running the calculations and Biovia for providing the computational software. We also thank L. A. Villaescusa for helpful comments.

Details

Database :
OpenAIRE
Journal :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Accession number :
edsair.doi.dedup.....6dc5fc9e9c2e6532999b4440d9c6cff8