Issue 33, 2016

An experimental and theoretical study of the aggregate structure of calix[6]arenes in Langmuir films at the water/air interface

Abstract

In this paper, the aggregate formation of para-tert-butylcalix[6]arene molecules (Calix6) in dimeric structures was investigated at the water/air interface using experimental and theoretical studies. A specific orientation for such Calix6 molecules was observed with an average area of 133 Å2, which corresponds to a flat-on orientation with the OH groups parallel to the interface. By varying the pressure on the Calix6 monolayer, the molecules tend to organize at the water/air interface and subsequently, at higher pressures, aggregates were formed atop the monolayer as cluster structures. Morphological characterization by the Brewster Angle Microscopy technique showed the formation of larger domains at lower pressures. Based on such experimental evidence, molecular dynamics (MD) simulations were performed to investigate possible dimeric structures for aggregated Calix6 molecules, which are localized at the water/air interface, where one molecule remains in the water phase and the other remains in the air phase. By increasing surface pressure, experimental and theoretical results corroborate the intermolecular interactions among Calix6 molecules. These results are relevant because a dimeric structure has a molecular cavity, which is a candidate for host–guest chemistry, an ion receptor or a drug-delivery system.

Graphical abstract: An experimental and theoretical study of the aggregate structure of calix[6]arenes in Langmuir films at the water/air interface

Supplementary files

Article information

Article type
Paper
Submitted
29 Jun 2016
Accepted
21 Jul 2016
First published
21 Jul 2016

Phys. Chem. Chem. Phys., 2016,18, 22906-22913

An experimental and theoretical study of the aggregate structure of calix[6]arenes in Langmuir films at the water/air interface

L. S. de Lara, E. C. Wrobel, M. Lazzarotto, S. R. de Lázaro, A. Camilo and K. Wohnrath, Phys. Chem. Chem. Phys., 2016, 18, 22906 DOI: 10.1039/C6CP04565K

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