Langmuir films and Langmuir-Blodgett multilayers incorporating mechanically-threaded molecules-pseudorotaxanes

This paper describes the synthesis of a π-electron rich aromatic lipid containing a polyether thread intercepted by a 1,5-dioxynaphthalene moiety. The terminus of one end of the polyether is a methoxyl group and the other a glycerol unit linked via the 2-oxo position, while the 1,3-oxo functions are covalently attached to octadecyl chains. This compound, when cospread at the air-water interface with the tetracationic cyclophane, cyclobis(paraquat-p-phenylene), and the phospholipid, dimyristoylphosphatidic acid, as its monoanion, forms self-assembled pseudorotaxanes which are self-organized into a two-dimensional supramolecular array at the interface. The electrostatic interactions between t…

Liquid crystalline side chain polymers containing photoreactive azobenzene chromophores in the dark-adapted trans form and phenylbenzoate groups as co-mesogens have been prepared and investigated as monomolecular layers at the water/air interface and as multilayer assemblies deposited onto solid supports by the Langmuir–Blodgett–Kuhn (LBK) technique. Pressure area isotherms at variable temperatures together with reflection absorption spectra and Brewster angle microscopic pictures have been taken and analyzed (i) to derive information about the structural order and the packing properties of the mesogenic side groups within the monolayers of different homo- and co-polymeric systems and ii) t…

Molecular Recognition-Induced Function and Competitive Replacement by Hydrogen-Bonding Interactions:  Amphiphilic Barbituric Acid Derivatives, 2,4,6-Triaminopyrimidine, and Related Structures at the Air−Water Interface

The phenomenon of molecular recognition inducing further function is common in nature. However, there are few synthetic systems which achieve this cascade type mechanism, and those are generally ca...

Protein interactions with ordered lipid films: Specific and unspecific binding

Structural Characterization of Monolayers at the air-water interface

Photoinduced electron transfer in molecular organizates at the gas-water interface

Abstract The influence of the molecular geometry is of fundamental importance for a better understanding of the photoinduced electron transfer mechanism. Because of their typical molecular structures, cyclophane rings have proved to be suitable for this purpose as electron acceptor molecules adsorbed under an amphiphile monolayer. We used a pyrene-labelled phospholipid derivative both as molecular anchor for the cyclophane ring and electron donor molecule. The co-spreading technique was used to prepare the complex monolayers. Surface pressure and surface potential measurements have indicated similar monolayer behaviour as with dimyristoylphosphatidic acid as anchor molecule, leading to the …