Sound focusing in rooms: the time-reversal approach

New perspectives in audible range acoustics, such as virtual sound space creation and active noise control, rely on the ability of the rendering system to recreate precisely a desired sound field. This ability to control sound in a given volume of a room is directly linked to the capacity to focus acoustical energy both in space and time. However, sound focusing in rooms remains a complicated problem, essentially because of the multiple reflections on obstacles and walls occurring during propagation. In this paper, the technique of time-reversal focusing, well known in ultrasound, is experimentally applied to audible range acoustics. Compared to classical focusing techniques such as delay law focusing, time reversal appears to considerably improve quality of both temporal and spatial focusing. This so-called super-resolution phenomenon is due to the ability of time reversal to take into account all of the different sound paths between the emitting antenna and the focal point, thus creating an adaptive spatial and temporal matched filter for the considered propagation medium. Experiments emphasize the strong robustness of time-reversal focusing towards small modifications in the medium, such as people in motion or temperature variations. Sound focusing through walls using the time-reversal approach is also experimentally demonstrated.     

Chiral-at-metal ruthenium complex as a metalloligand for asymmetric catalysis

The mononuclear [Ru(bpy)(2)(bpym)][PF(6)](2) complex (bpy = 2,2'-bipyridine; bpym = 2,2'-bipyrimidine) has been prepared in its enantiopure Lambda form. Because of the chelating property of the bipyrimidine moiety, it is possible to use this chiral-at-metal complex as a chiral inorganic ligand for a second metal cation acting as a catalytic center. Here we report the synthesis and the structural characterization of a novel dinuclear Lambda-[(bpy)(2)Ru(bpym)RuCl(p-cymene)](3+) compound (1). The asymmetric-inducing properties of the enantiopure chiral-at-metal metalloligand have been probed during asymmetric transfer hydrogenation to ketones catalyzed by 1. This provides one of the very few illustrations of the potential of this original class of chiral inorganic ligands.