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Peer-reviewedCC BY-NC 4.0Chemistry (Weinheim an Der Bergstrasse, Germany)

Synthesis, Physicochemical Characteristics, Self‐Assembly and Encapsulation Ability of per‐Ethylene‐Glycol‐Functionalized Resorcin[4]Arenes and Their Molecular Capsules: On the Road to Liquid Capsules

  1. 1School of Chemistry The Faculty of Exact Sciences Tel Aviv University Ramat Aviv Israel

Abstract

Self‐assembled molecular cages and capsules attracted considerable attention, owing to their unique structures and ability to function as nano‐reactors and catalysts. In recent years, porous liquids have emerged into an intriguing class of functional materials. Herein, we prepared a series of per‐ethylene‐glycol (EG)‐functionalized resorcin[4]arene hosts, bearing side chains with three, four, or five EG units (compounds 1d, 1e, and 1f, respectively). We studied their melting points, solubility, self‐assembly, and encapsulation abilities. Interestingly, 1e and 1f were found to be viscous liquids at RT and compound 1d melts at 104°C–105°C, while alkyl‐substituted resorcin[4]arenes (1a and 1c) melt at ∼300°C. We found in contrast to expectations, that the number of EG groups on the side chains affects the self‐assembly, the stability of the formed aggregates, and the encapsulation power of those systems in organic solvents. System 1d behaved, in CDCl3, much like alkyl‐substituted resorcin[4]arenes, forming self‐assembled hexameric capsules of comparable stability and size capable of encapsulating even tetra‐hexyl ammonium salts. Compounds 1e and 1f, however, form, in CDCl3, hexameric capsules, which are more dynamic than the capsules of 1c or even 1d that encapsulate smaller ammonium salts and appear to be promising candidates for the preparation of liquid capsules and capsular liquids.

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BibTeX
@article{angajala2026synthesis,
  title = {{Synthesis, Physicochemical Characteristics, Self‐Assembly and Encapsulation Ability of per‐Ethylene‐Glycol‐Functionalized Resorcin[4]Arenes and Their Molecular Capsules: On the Road to Liquid Capsules}},
  author = {Gangadhara Angajala and Inbar Horin and Tamar Evan‐Salem and Yoram Cohen},
  journal = {Chemistry (Weinheim an Der Bergstrasse, Germany)},
  year = {2026},
  month = jul,
  doi = {10.1002/chem.71489},
  url = {https://doi.org/10.1002/chem.71489},
  note = {CC BY-NC 4.0},
}
RIS
TY  - JOUR
TI  - Synthesis, Physicochemical Characteristics, Self‐Assembly and Encapsulation Ability of per‐Ethylene‐Glycol‐Functionalized Resorcin[4]Arenes and Their Molecular Capsules: On the Road to Liquid Capsules
AU  - Gangadhara Angajala
AU  - Inbar Horin
AU  - Tamar Evan‐Salem
AU  - Yoram Cohen
PY  - 2026
DA  - 2026/07/30
JO  - Chemistry (Weinheim an Der Bergstrasse, Germany)
DO  - 10.1002/chem.71489
UR  - https://doi.org/10.1002/chem.71489
AB  - Self‐assembled molecular cages and capsules attracted considerable attention, owing to their unique structures and ability to function as nano‐reactors and catalysts. In recent years, porous liquids have emerged into an intriguing class of functional materials. Herein, we prepared a series of per‐ethylene‐glycol (EG)‐functionalized resorcin[4]arene hosts, bearing side chains with three, four, or five EG units (compounds 1d, 1e, and 1f, respectively). We studied their melting points, solubility, self‐assembly, and encapsulation abilities. Interestingly, 1e and 1f were found to be viscous liquids at RT and compound 1d melts at 104°C–105°C, while alkyl‐substituted resorcin[4]arenes (1a and 1c) melt at ∼300°C. We found in contrast to expectations, that the number of EG groups on the side chains affects the self‐assembly, the stability of the formed aggregates, and the encapsulation power of those systems in organic solvents. System 1d behaved, in CDCl3, much like alkyl‐substituted resorcin[4]arenes, forming self‐assembled hexameric capsules of comparable stability and size capable of encapsulating even tetra‐hexyl ammonium salts. Compounds 1e and 1f, however, form, in CDCl3, hexameric capsules, which are more dynamic than the capsules of 1c or even 1d that encapsulate smaller ammonium salts and appear to be promising candidates for the preparation of liquid capsules and capsular liquids.
SN  - 0947-6539
SN  - 1521-3765
ER  -