Size dependence of molecular self-assembling in stacked aggregates. 2. Heat exchange effects.
J Phys Chem B
; 117(30): 9083-93, 2013 Aug 01.
Article
en En
| MEDLINE
| ID: mdl-23837441
ABSTRACT
Many aromatic molecules self-associate in aqueous solutions into dimers, trimers, and higher order one-dimensional aggregates. They self-assemble due to the π-π stacking interactions in supramolecular structures with a length distribution determined by the size-dependent association equilibrium constants. Due to their low solubility, in many experiments the aromatic molecules are dissolved in their cationic form. The presence of the localized positive charge promotes a new type of binding led by the cation-π interaction. Accordingly, in the case of aromatic molecules dissolved in water in their cationic form, at least two types of aggregates may appear the rodlike aggregates stabilized by π-π stacking, and dimers coupled by the cation-π interaction. The heat exchange which accompanies the association (dissociation) processes offers the most direct way to determine the characteristic thermodynamic parameters. The heat exchange that arises at each dissociation event has been measured by isothermal titration calorimetry (ITC) on a test molecule whose self-association properties are already known ciprofloxacin hydrochloride. The fitting protocol relies on the recently developed DK self-association model which describes in a rigorous manner the size distribution of molecular aggregates in solution.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Tipo de estudio:
Prognostic_studies
Idioma:
En
Revista:
J Phys Chem B
Asunto de la revista:
QUIMICA
Año:
2013
Tipo del documento:
Article
País de afiliación:
Rumanía
Pais de publicación:
EEUU
/
ESTADOS UNIDOS
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ESTADOS UNIDOS DA AMERICA
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EUA
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UNITED STATES
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UNITED STATES OF AMERICA
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US
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USA