Chain dynamics of surfactants in mesoporous silica

• Published in: Physical chemistry chemical physics : PCCP Vol. 15; no. 42; pp. 18620 - 18626
• Main Authors: Kharkov, B B, Dvinskikh, S V
• Format: Journal Article
• Language: English
• Published: England 01.01.2013
• Subjects: Adjustable; Arrays; C-13 Nmr; Chains; Diffusion; Dynamic structural analysis; Dynamics; Fast Mas; Heteronuclear Dipolar Couplings; Lipid-Bilayers; Liquid-Crystals; Mesophase; Mesostructured Materials; Order parameters; Polarization Transfer; Silicon dioxide; Solid-State Nmr; Spectroscopy; Surfactants
• ISSN: 1463-9076; 1463-9084; 1463-9084
• DOI: 10.1039/c3cp52562g

Mesostructured porous materials possess unique surface, structural, and bulk properties that lead to important practical applications. By retaining structure-directing species in the product material, mesostructured organic-inorganic composites are obtained which are of broad interest for fundamental studies of confinement effects and surface interaction on structural and dynamic properties of organic molecules. In the present study, solid state dipolar (13)C-(1)H NMR spectroscopy is applied to quantitatively characterize the conformational dynamics of organic surfactants in the mesostructured composite CTAB-MCM41. Such an approach does not require assumptions and adjustable parameters and reflects the changes in conformational dynamics without relying on specific motional models. The conformational dynamics of the surfactant confined in solid hexagonal arrays is compared to that in hexagonal aggregates formed in a concentrated aqueous solution. The study showed that in cylindrical pores of hexagonal mesoporous silica the order parameter gradually decreases towards the end of the chain. The degree of order and the order parameter profile is similar to that observed in hexagonal liquid crystalline phases. However, the mobility of segments close to the head group is more restricted compared to that in the mesophase, as the result of interaction with the solid silica interface.