Molecular recognition controls the organization of mixed self-organized bis-urea-based mineralization templates for CaCO(3)

To investigate the role and importance of nondirectional electrostatic interactions in mineralization, we explored the use of Langmuir monolayers in which the charge density can be tuned using supramolecular interactions. It is demonstrated that, in mixed Langmuir monolayers of bis-ureido surfactant...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1991. - 23(2007), 25 vom: 04. Dez., Seite 12655-62
1. Verfasser: Pichon, Benoît P (VerfasserIn)
Weitere Verfasser: Cantin, Sophie, Smulders, Maarten M J, Vos, Matthijn R J, Chebotareva, Natalia, Popescu, Daniela C, van Asselen, Otto, Perrot, Françoise, Sijbesma, Rint, Sommerdijk, Nico A J M
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Membranes, Artificial Quaternary Ammonium Compounds Surface-Active Agents Polyethylene Glycols 3WJQ0SDW1A Urea 8W8T17847W Calcium Carbonate H0G9379FGK
Beschreibung
Zusammenfassung:To investigate the role and importance of nondirectional electrostatic interactions in mineralization, we explored the use of Langmuir monolayers in which the charge density can be tuned using supramolecular interactions. It is demonstrated that, in mixed Langmuir monolayers of bis-ureido surfactants containing oligo(ethylene oxide) and ammonium head groups associated with matching or nonmatching spacers between the two urea groups, the organization is controlled by molecular recognition. These different organizations of the molecules lead to different nucleation behavior in the mineralization of calcium carbonate. The formation of modified calcite and vaterite crystals was induced selectively by different phases of mixed monolayers, and they were characterized by SEM, TEM, and SAED. To understand the influence of the mixed Langmuir monolayers on the crystallization process, we studied the mixtures by means of (pi-A) isotherms and Brewster angle microscopy observations. Infrared reflection-absorption spectroscopy experiments were also performed on Langmuir-Schaefer films. From these results, we conclude that the local organization of the two systems discussed here gives rise to differences in both charge density and flexibility that together determine not only polymorph selection and the nucleation face but also the morphology of the resulting crystals
Beschreibung:Date Completed 08.01.2008
Date Revised 01.12.2018
published: Print-Electronic
Citation Status MEDLINE
ISSN:0743-7463