From nucleobases to nucleolipids: an ITC approach on the thermodynamics of their interactions in aqueous solutions.

Hybrid constructions based on nucleosides and lipophilic components, known as nucleolipids, have become an extremely interesting class of molecules, especially for their potential biomedical applications. In this matter, it seemed important to define the nature and estimate the strength of their interaction with polynucleotides by different ways. We report in this work a systematic investigation through isothermal titration calorimetry of the thermodynamics of the association and dissociation of adenine and thymine derivatives, not previously performed.

Control of the PEO chain conformation on nanoparticles by adsorption of PEO-block-poly(L-lysine) copolymers and its significance on colloidal stability and protein repellency.

The physical adsorption of PEO(n)-b-PLL(m) copolymers onto silica nanoparticles and the related properties of poly(ethylene oxide) (PEO)-coated particles were studied as a function of the block copolymer composition. Copolymers adopt an anchor-buoy conformation at the particle surface owing to a preferential affinity of poly(L-lysine) (PLL) blocks with the silica surface over PEO blocks when a large excess of copolymer is used. The interdistance between PEO chains at particle surface is highly dependent on the size of PLL segments; a dense brush of PEO is obtained for short PLL blocks (DP = 10), whereas PEO chains adopt a so-called interacting "mushroom" conformation for large PLL blocks (DP = 270).

A physico-chemical investigation of poly(ethylene oxide)-block-poly(L-lysine) copolymer adsorption onto silica nanoparticles.

The adsorption behavior of poly(ethylene oxide)-b-poly(L-lysine) (PEO(113)-b-PLL(10)) copolymer onto silica nanoparticles was investigated in phosphate buffer at pH 7.4 by means of dynamic light scattering, zeta potential, adsorption isotherms and microcalorimetry measurements. Both blocks have an affinity for the silica surface through hydrogen bonding (PEO and PLL) or electrostatic interactions (PLL).

Effective strength of the electron-electron interaction in simultaneous projectile and target ionization.

The determination of the right balance between the strong-field interaction of the screened target nucleus and the two-center electron-electron interaction has been controversial since the early attempts to describe the stripping of light, swift ions, by heavy targets. In this work, we find a region of influence for the electron-electron contribution which clearly indicates that this interaction is an essential contribution to the stripping process for both light and heavy targets.

Phase behavior and blue-phase-III-isotropic critical point in (R)-(S) mixtures of a chiral liquid crystal with a direct twist-grain-boundary to blue-phase transition.

We have investigated mixtures of the (R) and (S) enantiomers of a chiral liquid crystal, (R)- or (S)-1-methylheptyl 3'-fluoro-4'-(3-fluoro-4-octadecyloxybenzoyloxy)tolane-4-carboxylate using high-resolution adiabatic scanning calorimetry. The pure (R) compound has a direct transition from the twist-grain-boundary to the blue phase without an intermediary chiral nematic phase. For the blue phases a different kind of phase behavior as a function of enantiomeric excess is observed, most probably related to the presence of a twist-grain-boundary-A instead of a chiral nematic phase below the blue phases.