Nature of the Metal Insulator Transition in High-Mobility 2D_Si-MOSFETs.

Our investigation focuses on the analysis of the conductive properties of high-mobility 2D-Si-MOSFETs as they approach the critical carrier density, nsc (approximately 0.72×1011 cm-2), which marks the metal insulator transition (MIT). In close proximity to the nsc, the conductivity exhibits a linear dependence on the temperature (T). By examining the extrapolated conductivity at the absolute zero temperature (T = 0), denoted as σ0, as a function of the electron density ns, we identify two distinct regimes with varying σ0(ns) patterns, indicating the existence of two different phases. The transition from one of these two regimes to another, coinciding with nsc, is abrupt and serves as the focus of our investigation. Our aim is to establish the possibility of a percolation type transition in the 2D-Si-MOSFETs' sample. In fact, we observed that the model of percolation is applicable only for densities very close to nsc*=n2 (where n2 is the linear extrapolation of σ0), indicating the percolation type transition essentially represents a phase transition at the zero temperature.

Chitosan-graft-polyaniline-based hydrogels: elaboration and properties.

Intrinsically conducting polymers are of great interest for a large number of applications. But among the major drawbacks are their low solubility in common solvents and their poor mechanical properties. Elaboration of composites associating a matrix, bringing its mechanical properties, and polyaniline, as the conducting polymer, is a way of overcoming these disadvantages. Chitosan-graft-polyaniline copolymers were synthesized by simple oxidative method. The grafting reaction was quite complete, and it was found that the copolymers cross-linked to yield a composite hydrogel in which the polyaniline was homogeneously embedded. The conductivity of precursor (block copolymer) and gels was found to be larger than 10(-2) S x cm(-1). The composite gels were characterized in terms of swelling and rheological properties. They can be classified as "superabsorbent" hydrogels, and the swelling is reversible. The composite gels were then successfully used as actuators.

Oxidation of sulfides and disulfides under electron transfer or singlet oxygen photosensitization using soluble or grafted sensitizers.

Two different photosensitizers, 9,10-dicyanoanthracene (DCA) and benzophenone (BzO) or a silica bound derivative (BzO-Si) have been compared for the photooxidation of di-n-butyl sulfide and di-n-butyl disulfide. With either photosensitizer, sulfide photooxidation in acetonitrile leads very efficiently to sulfoxide, with sulfone and disulfides as by-products. Although an electron transfer mechanism has previously been established starting with DCA, our results are indicative of two competitive mechanisms using BzO as the photosensitizer, instead of singlet oxygen addition and electron transfer. The more sluggish photooxidation of disulfides leads to a complex mixture of products, among which n-butyl butanethiosulfonate and strong acids (alkylsulfonic and sulfuric) are the major ones. The relative ratio thiosulfonate: acids depends, among other factors, on the medium polarity with acid formation favored starting with BzO or BzO-Si in a methanol-water mixture. An electron transfer mechanism only can account for the observed products Superoxide anion, the formation of which is much easier starting from BzO than from DCA, is suggested to play a crucial role in this oxidative radical pathway. Starting from disulfides, grafted benzophenone is more efficient for acid formation than its soluble counterpart. As this photosensitizer can easily be recycled, an easy and smooth way to acid formation is thus available, provided that the reaction solvent is properly chosen.