Molecular organization of cylindrical sexithiophene aggregates measured by X-ray scattering and magnetic alignment.

We have determined the internal organization of elongated sexithiophene aggregates in solution by combining small-angle X-ray scattering and magnetic birefringence experiments. The different aggregate axes can be probed independently by performing the experiments on magnetically aligned aggregates. We have found multiwalled cylindrical aggregates consisting of radially oriented sexithiophene molecules with pi-pi-stacking in the tangential direction, a structure that is considerably different from those previously found in other solvents.

The role of heterogeneous nucleation in the self-assembly of oligothiophenes.

The cooperative self-assembly of oligothiophenes can be characterized by heterogeneous nucleation caused by trace amounts of impurities leading to a manifold of supramolecular arrangements.

Anharmonic magnetic deformation of self-assembled molecular nanocapsules.

High magnetic fields were used to deform spherical nanocapsules, self-assembled from bolaamphiphilic sexithiophene molecules. At low fields the deformation--measured through linear birefringence-scales quadratically with the capsule radius and with the magnetic field strength. These data confirm a long standing theoretical prediction [W.

Chiral amphiphilic self-assembled alpha,alpha'-linked quinque-, sexi-, and septithiophenes: synthesis, stability and odd-even effects.

The synthesis, characterization, and self-assembly in butanol of a series of well-defined alpha,alpha'-linked quinqui-, sexi-, and septithiophenes substituted, via ester links at their termini, by chiral oligo(ethylene oxide) chains carrying an alpha, beta, delta, and epsilon methyl, respectively, are reported. Studies of the self-assembly of these molecules using UV/visible absorption, luminescence, and circular dichroism spectroscopies reveal, for the sexithiophene case, that the magnitude of the observed Cotton effect in the aggregates diminishes progressively as the chiral substituent is moved away from the thiophene segment. The stability of the assemblies increases with the length of the oligothiophene and as the substituent chiral unit is moved away from the aromatic core, being greatest for the unsubstituted case.

Observations on the adherence of Proteus mirabilis onto polymer surfaces.

Aims: Infection of the catheterized urinary tract with Proteus mirabilis causes blockage of the catheter by crystalline bacterial biofilms. The aim of this work is to identify a surface-coating for catheters that is not vulnerable to colonization by Pr. mirabilis.

Molecule-molecule versus molecule-substrate interactions in the assembly of oligothiophenes at surfaces.

In this paper we present a joint experimental and theoretical approach for the study of the assembly of end-substituted oligothiophenes at surfaces with different polarities (i.e., mica vs graphite).

Magnetic deformation of self-assembled sexithiophene spherical nanocapsules.

We report the experimental observation of magnetic field deformation of spherical nanocapsules, self-assembled from sexithiophene molecules, into oblate spheroids, confirming a long-standing theoretical prediction. The magnetically deformed objects can be trapped in a compatible organogel to make them suitable for further investigations and applications. Our results show that strong magnetic forces can be effectively used, in a contact-free manner, as a tool to control the self-organization of a whole class of functional organic molecules.

Polymer surface properties and their effect on the adhesion of Proteus mirabilis.

A problem encountered in patients undergoing long-term catheterization of the urinary tract is that of encrustation and blockage of the catheter by crystalline bacterial biofilms. This is principally caused by the action of the urease-producing pathogen Proteus mirabilis. A major aim of this work is to develop materials resistant to encrustation.

Poly(distyrylbenzene-block-sexi(ethylene oxide)), a highly luminescent processable derivative of PPV.

A block copolymer of distyrylbenzene with sexi(ethylene oxide) spacers displays high solid state photoluminescence efficiency (34%). Single layer light-emitting diodes with calcium or aluminium cathodes exhibit luminances over 2000 cd m-2 and efficiencies of 0.5 cd A-1.

Supramolecular organization of alpha,alpha'-disubstituted sexithiophenes.

The self-assembly of alpha,alpha'-linked sexithiophenes with chiral and achiral penta(ethylene glycol) chains attached at the alpha-positions of the terminal rings, that is, 2,2':5',2'':5'',2''':5''',2'''':5'''',2'''''-sexithiophene-5,5'''''-dicarboxylic acid-2S)-2-methyl-3,6,9,12,15-pentaoxahexadecyl ester (1) and 2,2':5',2'':5'',2''':5'''',2''''':5''''',2'''''-sexithiophene-5,5'''''-dicarboxylic acid-3,6,9,12,15-pentaoxahexadecyl ester (2), respectively is described. Analysis of the UV/vis, fluorescence, circular dichroism, and circular polarization of luminescence spectroscopic data shows that these compounds form chiral aggregates in polar solvents and in the solid state. In n-butanol aggregation occurs at temperatures below 30 degrees C, while above this threshold temperature the aggregates break up without an intermediate disordered state of aggregation, and the compounds are molecularly dissolved.