Charge transport in self-organized pi-stacks of p-phenylene vinylene oligomers

We have studied the mobility of charge carriers along self-organizing pi-stacks of hydrogen-bonded phenylene vinylene oligomers in solution, by time-resolved microwave conductivity measurements. The value deduced for the mobility along the stacks is 3 x 10(-3) and 9 x 10(-3) cm2/(V s) for holes and electrons, respectively. Additionally, we have calculated the mobility along the pi-stacks using a hopping model based on parameters from density functional theory. The mobility values obtained from these calculations are in good agreement with the experimental values if it is assumed that there are relatively large twist angles between neighboring molecules in the stack. It is shown that a significantly higher mobility can be attained if the twist angle between neighboring oligomers is reduced.     

Reversible destruction of dynamical localization

Dynamical localization is a localization phenomenon taking place, for example, in the quantum periodically driven kicked rotor. It is due to subtle quantum destructive interferences and is thus of intrinsic quantum origin. It has been shown that deviation from strict periodicity in the driving rapidly destroys dynamical localization. We report experimental results showing that this destruction is partially reversible when the deterministic perturbation that destroyed it is slowly reversed. We also provide an explanation for the partial character of the reversibility.     

Unravelling the mechanism of RNA-polymerase forward motion by using mechanical force

Polymerases form a class of enzymes that act as molecular motors as they move along their nucleic acid substrate during catalysis, incorporating nucleotide triphosphates at the end of the growing chain and consuming chemical energy. A debated issue is how the enzyme converts chemical energy into motion [J. Gelles and R. Landick, Cell 93, 13 (1998)]. In a single molecule assay, we studied how an opposing mechanical force affects the translocation rate of T7 RNA polymerase. Our measurements show that force acts as a competitive inhibitor of nucleotide binding. This result is interpreted in the context of possible models, and with respect to published crystal structures of T7 RNA polymerase. The transcribing complex appears to utilize only a small fraction of the energy of hydrolysis to perform mechanical work, with the remainder being converted to heat.     

Ruderman-Kittel-Kasuya-Yosida and magnetic-field interactions in coupled Kondo quantum dots

We investigate theoretically the transport properties of two independent artificial Kondo impurities. They are coupled together via a tunable Ruderman-Kittel-Kasuya-Yosida (RKKY) interaction. For strong enough antiferromagnetic RKKY interaction, the impurity density of states increases with the applied in-plane magnetic-field. This effect can be used to distinguish between antiferromagnetic and ferromagnetic RKKY interactions. These results may be relevant to explain some features of recent experiments by Craig et al. [Science 304, 565 (2004)].     

Experimental observation of the elliptically polarized fundamental vector soliton of isotropic Kerr media

We report the experimental observation of the elliptically polarized fundamental vector soliton of isotropic Kerr media and its unique polarization evolution. This was achieved in the spatial domain in a nonbirefringent CS2 planar waveguide.     

Nonlinear effects of non-Newtonian fluids on natural convection in a porous medium

This paper investigates the rheological effects of non-Newtonian fluids on the natural convection mechanism in a porous medium. A non-Newtonian behavior of power law fluid with a yield stress, saturating a porous medium, in which yield stress is temperature dependent, is considered. The cases of constant temperature boundary and constant heat flux boundary, along the heated vertical cylinder, are analyzed. The approximate similarity solutions in a closed form are shown, from which the velocity and temperature profiles are determined. The numerical solutions for a constant temperature boundary are also shown and discussed.     

Highly Diastereo‐ and Enantioselective Synthesis of Cyclohepta[b]indoles by Chiral‐Phosphoric‐Acid‐Catalyzed (4+3) Cycloaddition

A highly enantio‐ and diastereoselective formal (4+3) cycloaddition of 1,3‐diene‐1‐carbamates with 3‐indolylmethanols in the presence of a chiral phosphoric acid catalyst is reported. The approach described herein provides efficient access to 6‐aminotetrahydrocyclohepta[b]indoles in good yields with mostly complete diastereoselectivity and excellent levels of enantioselectivity (>98:2 dr and up to 98 % ee). Mild reaction conditions, facile scale‐up, and versatile derivatization highlight the practicality of this methodology. A mechanistic study suggests that cycloaddition occurs in a stepwise fashion, after the formation of an ion pair between the chiral catalytic phosphate and the intermediate carbocation.