Search results for "Amphiphilic molecule"

Supramolecular Aggregates in Vacuum: Positively Mono-Charged Sodium Alkanesulfonate Clusters

2010

The formation and structural features of positively mono-charged aggregates of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) and sodium methane—(MetS), butane—(ButS) and octane—(OctS) sulfonate molecules in the gas phase have been investigated by electrospray ionization mass spectrometry, energy-resolved mass spectrometry and density functional theory (DFT) calculations. The experimental results show that the center-of-mass collision energy required to dissociate 50% of these mono-charged aggregates scantly depends on the length of the alkyl chain as well as on the aggregation number. This, together with the large predominance of mono-charged species in the mass spectra, was rationalized i…

Microspectroscopy on single domains of phase-separated monolayers

1989

SUMMARY A versatile and inexpensive, but fully equipped apparatus is presented, which enables detailed optical studies on amphiphilic molecules at the liquid-gas interface. Structural and spectroscopic information, particularly in small areas of single domains of phase-separated monolayers, can be achieved by combination of this miniaturized Langmuir trough and spectralphotometer microscope. The potential of this apparatus is demonstrated with some measurements on a diyne-substituted polymerizable lipid analogue at the air-water interface.

Immobilization of functionalized lipids in a random poly(methacrylate) copolymer monolayer

1995

It is shown that a monolayer of random poly(methacrylate) copolymer with a hydrophobic and a hydrophilic substituent exhibits a transition from the fluid to amorphous state. Above this transition any amphiphilic molecules mixed with the monolayer are immobile. Furthermore, such functionalized lipids are immobilized in the monolayer during the Langmuir-Blodgett transfer. The hydrophilic head-groups of the biotin-lipids remain on the formerly water-adjacent side of the monolayer, even if this side is exposed to air

How self-assembly of amphiphilic molecules can generate complexity in the nanoscale

2015

Abstract Given the importance of nanomaterials and nanostructures in modern technology, in the past decades much effort has been directed to set up efficient bottom up protocols for the piloted self-assembly of molecules. However, molecules are generally disinclined to adopt the desired structural organization because they behave according to their own specific intermolecular interactions. Thus, only some selected classes of chemical compounds are capable to lead to useful self-assembled structures. Amphiphiles, simultaneously possessing polar and apolar moieties within their molecular architecture, can give a wide scenario of possible intermolecular interactions: polar–polar, polar–apolar,…

Optical Studies of Amphiphilic Molecules with Interesting Electro-Optical and Non-Linear Optical Properties

1990

Structural control is a major issue in both life science, investigating the function of the biological machinery, and in materials science, aiming at the design of novel devices. In part one, recent electro-optical investigations of the primary event of photosynthesis on purified protein preparations are described. Part two focuses on structural studies of monolayers at an air/water interface, and of Langmuir-Blodgett multilayers from a new molecule designed for nonlinear optical applications.

Mixed Valence Materials: Prussian Blue Analogues of Reduced Dimensionality (Small 16/2012)

2012

Monolayers of Amphiphilic Molecules

1992

There are good reasons why the organizers have placed this lecture at the beginning of a conference on the multip1e aspects of membranes. In many respects the monolayer may be considered half of a membrane and it obviously is the most simple and best-defined model system. Yet we will show that the system is more complex than many have anticipated. On the other hand, there are many general features which can be discussed without looking into chemical details.

Theoretical modeling of Langmuir monolayers

1999

Abstract We study coarse-grained continuum models for Langmuir monolayers by self-consistent field theory and by Monte Carlo simulations. Amphiphilic molecules are represented by stiff chains of monomers with one end grafted to a planar surface. In particular, we discuss the origin of successive fluid–fluid transitions, the possible origin of tilt order and the factors which determine the direction of tilt.