http://www.cnr.it/ontology/cnr/individuo/prodotto/ID195137
Competition Between Gelation and Crystallisation of a Peculiar Multicomponent Liquid System Based on Ammonium Salts (Articolo in rivista)
- Type
- Label
- Competition Between Gelation and Crystallisation of a Peculiar Multicomponent Liquid System Based on Ammonium Salts (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/c2sm07183e (literal)
- Alternative label
I. Kapoor, E.-M. Schön, J. Bachl, D. Kühbeck, C. Cativiela, S. Saha, R. Banerjee, S. Roelens, J. J. Marrero-Tellado, D. Díaz Díaz (2012)
Competition Between Gelation and Crystallisation of a Peculiar Multicomponent Liquid System Based on Ammonium Salts
in Soft matter (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- I. Kapoor, E.-M. Schön, J. Bachl, D. Kühbeck, C. Cativiela, S. Saha, R. Banerjee, S. Roelens, J. J. Marrero-Tellado, D. Díaz Díaz (literal)
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- Pagina fine
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- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Institut fur Organische Chemie, Universitat Regensburg, Germany;
Instituto de Sintesis Quimica y Catalisis Homogenea (ISQCH), CSIC-Universidad de Zaragoza, Spain;
Physical/Materials Chemistry Division, National Chemical Laboratory, India;
Istituto di Metodologie Chimiche (IMC), Consiglio Nazionale delle Ricerche (CNR), Italy;
Instituto Universitario de Bio-Organica ''Antonio Gonzalez'', Universidad de La Laguna, Spain; (literal)
- Titolo
- Competition Between Gelation and Crystallisation of a Peculiar Multicomponent Liquid System Based on Ammonium Salts (literal)
- Abstract
- An exemplar competition between gelation and crystallisation phenomena was examined with an
unusual synergistic multicomponent (organo)gelator solution (MGS), which consists of a well-defined
methanolic solution of (1R,2R)-1,2-diaminocyclohexane L-tartrate containing 2.4 equiv. of
concentrated hydrochloric acid. The optimal composition of the MGS was determined through
meticulous solubility, gelation and structural studies, which support a transient gelation mechanism
based on the kinetic self-assembly of the tartrate salt driven by hydrogen-bonding interactions,
involving ammonium nitrogen donors and hydroxyl oxygen acceptors, and electrostatic interactions.
The hydrochloric acid is involved in the solubilisation of the salt through an ionic dissociationexchange
process, which ends up with the formation-precipitation of (1R,2R)-1,2-diaminocyclohexane
dihydrochloride. As a consequence, an irreversible destruction of the gel takes place, which indicates
the metastable nature of this phase that cannot be accessed from the thermodynamically equilibrated
state. Gelation of a variety of oxygenated and nitrogenated solvents with moderate polarity occurred
efficiently using extremely low MGS concentrations at low temperatures, and the gel phase was
confirmed by dynamic rheological measurements. Several features make the described MGS unique: (1)
it is a multicomponent solution where each component and its stoichiometry play a key role in the
reproducible formation and stabilization of the gels; (2) it is formed by simple, small, and commercially
available chiral building blocks (dissolved in a well-defined solvent system), which are easily amenable
for further modifications; (3) the gelation phenomenon takes place efficiently at low temperature upon
warming up the isotropic solution, conversely to the typical gel preparation protocol; and (4) the
formed organogels are not thermoreversible despite the non-covalent interactions that characterize the
3D-network (literal)
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