Thermodynamics, morphology and molecular structure of molecular compounds in trisamide triarylamine organogels and pseudo-organogels.

In this paper, potentially-gelling binary systems are investigated by DSC, X-ray and Electron microscopy in order to assess their gel status and the role of the Hansen solubility parameter. The low molecular weight organogelator is a Triarylamine Trisamide (TATA) while the solvents consist of a series of halogeno-ethanes and of toluene. Temperature-concentration phase diagrams are mapped out from DSC traces.

Some Remarkable Rheological and Conducting Properties of Hybrid PVC Thermoreversible Gels/Organogels.

We report on investigations into the rheological properties of organogels prepared from triarylamine trisamide (TATA) and oligo phenylene vinylene (OPVOH) molecules in binary organogel gels and in ternary thermoreversible networks with poly vinyl chloride (PVC). In the case of OPVOH, we show that the modulus of the ternary gel is simply the sum of the modulus of each binary gel, corresponding to the so-called Voigt upper limit. In contrast, TATA/PVC ternary gels generally exceed the Voigt upper limit.

Evidence by neutron diffraction of molecular compounds in triarylamine tris-amide organogels and in their hybrid thermoreversible gels with PVC.

We report on neutron diffraction experiments performed on organogels prepared from triarylamine tris-amide (TATA), as well as on their ternary thermoreversible gels made up with poly[vinyl chloride] (PVC). Three different solvents together with their deuterated counterparts have been used; tetrachloroethane, wherein TATA fibrils display ohmic conductivity, bromobenzene and -dichlorobenzene. The TATA crystal structure differs in the three solvents.

Physical Aspects of Organogelation: A Point of View.

The physics side of organogelation is broached through three main aspects, thermodynamics (formation and melting), structure (morphology and molecular organization), and rheology. A definition of a gel is first discussed so as to delimit the field of investigation; namely, systems constituted of fibril-like entities. It is again highlighted that gel formation occurs through first-order transitions, chiefly by homogeneous nucleation.

Hybrid Physical Gels from Polymers and Self-Assembled Systems: A Novel Path for Making Functional Materials.

In recent years, the synthesis of novel organic molecules that spontaneously self-assemble into a large variety of molecular architecture, particularly the formation of organogels, has yielded new opportunities in the preparation of functional materials. Here, we present an original preparation path of such materials through the fabrication of hybrid gels of these molecules with covalent polymers. Three types of systems are described: (i) intermingled gels where a polymer gel and an organogel pervade one another; (ii) encapsulation of self-assembled filaments in polymer fibrils, which provides a system with unusual magnetic properties; (iii) the reverse situation in which self-assembled nanotubes sheathe polymer fibrils.