Rapid and facile one-step microwave synthesis of macrobicyclic cryptands

Liquid-assisted grinding (LAG) and microwave synthesis are proposed as alternative routes for the synthesis of cryptands, with reaction times of up to 16 times faster than traditional methods. These rapid and facile techniques have the potential to replace traditional methods for a high-yield formation of clathrochelates, and other materials. The cryptand 6,16,25-tribenza-1,4,8,11,14,18,23,27-octa-aza-tri-cyclo-[9.9.9]nona-cosa-4,7,14,17,23,26-hexaene hexa-hydrate, C<sub>36</sub>H<sub>42</sub>N<sub>8</sub>·6H<sub>2</sub>O, (<b>Ph<sub>3</sub>T<sub>2</sub></b> ) was synthesized using this novel method. The crystal structure was redetermined by single-crystal X-ray diffraction using synchrotron radiation at 120 K. The structure exhibits disorder in the water mol-ecule of hydration.

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Publication Details

Journal
Acta Crystallographica Section E Crystallographic Communications
Published
2025-04-07
DOI
https://doi.org/10.1107/s2056989025003044
Primary Topic
Mesoporous Materials and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Rapid and facile one-step microwave synthesis of macrobicyclic cryptands

U. Baisch, Liana Vella‐Żarb, Marie Christine Scicluna
Acta Crystallographica Section E Crystallographic Communications
Mesoporous Materials and Catalysis
article

Rapid and facile one-step microwave synthesis of macrobicyclic cryptands

U. Baisch, Liana Vella‐Żarb, Marie Christine Scicluna
article en

Abstract

Liquid-assisted grinding (LAG) and microwave synthesis are proposed as alternative routes for the synthesis of cryptands, with reaction times of up to 16 times faster than traditional methods. These rapid and facile techniques have the potential to replace traditional methods for a high-yield formation of clathrochelates, and other materials. The cryptand 6,16,25-tribenza-1,4,8,11,14,18,23,27-octa-aza-tri-cyclo-[9.9.9]nona-cosa-4,7,14,17,23,26-hexaene hexa-hydrate, C<sub>36</sub>H<sub>42</sub>N<sub>8</sub>·6H<sub>2</sub>O, (<b>Ph<sub>3</sub>T<sub>2</sub></b> ) was synthesized using this novel method. The crystal structure was redetermined by single-crystal X-ray diffraction using synchrotron radiation at 120 K. The structure exhibits disorder in the water mol-ecule of hydration.

Acta Crystallographica Section E Crystallographic CommunicationsVol. 81(5)
University of Malta (MT)
European Commission, European Regional Development Fund, European Social Fund
Clean water and sanitation
Openalex Percentile: Top 94%
Mesoporous Materials and Catalysis
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