Donor-acceptor-promoted gelation of polyaromatic compounds
Low molecular mass organogels are nonconventional polymeric structures in which a minute amount of low molecular weight compound can reversibly gelify the whole solution without forming covalent bonds between the monomers. In this article, we demonstrate that certain electron acceptors (taking dinit...
Veröffentlicht in: | Langmuir : the ACS journal of surfaces and colloids. - 1992. - 21(2005), 26 vom: 20. Dez., Seite 12130-8 |
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Weitere Verfasser: | , , , |
Format: | Aufsatz |
Sprache: | English |
Veröffentlicht: |
2005
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Zugriff auf das übergeordnete Werk: | Langmuir : the ACS journal of surfaces and colloids |
Schlagworte: | Journal Article Research Support, Non-U.S. Gov't Gels Polycyclic Compounds |
Zusammenfassung: | Low molecular mass organogels are nonconventional polymeric structures in which a minute amount of low molecular weight compound can reversibly gelify the whole solution without forming covalent bonds between the monomers. In this article, we demonstrate that certain electron acceptors (taking dinitrobenzoates as model compounds) that are incapable of gelifying the solvent on their own can assemble as much as a 15-16-fold larger amount of polyaromatic hydrocarbons (PAHs) and form two-component donor-acceptor organogels in different solvents. At the core of the long-range order stand donor-acceptor pairs. We assess our claims by detailed 1H NMR, spectrophotometry, fluorescence, and time-resolved fluorescence methods. The thermodynamics of the gelation process is described on the basis of temperature dependent 1H NMR studies. We believe that, in this case, 1H NMR provides direct quantification of the dissolved concentrations of the different species and therefore provides a direct way to measure the enthalpy, entropy, and free energy associated with gel formation |
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Beschreibung: | Date Completed 19.07.2007 Date Revised 13.12.2005 published: Print Citation Status MEDLINE |
ISSN: | 1520-5827 |