Los sistemas lacustres del Eoceno superior y Oligoceno del sector oriental de la Cuenca del Ebro

El relleno sedimentari de edad Priaboniense superior-Chattiense dcl sector oriental de la cuencade antepaís del Ebro puede subdividirse en cinco secuencias deposicionales, definidas en base a 1os principales cambios paleogeográficos que afectaron alos sistemas aluviales y lacustres en la región. Tanto el desarrollo de estructuras tectónicas superficiales como 1os procesos de ajuste isostático regional son considerados como 1os principales factores de control de esta evolución sedimentaria. Los cinco sistemas lacustres reconocidos (La Noguera, L'Anoia, Segarra, L'Urgell y Los Monegros) muestran unas caracteristicas de extensión areal y desarrollo de facies fuertemente controladas por su situación respecto a las zonas de máxima subsidencia. Las tendencias megasecuenciales de cambio o de alternancia de deposición evaporítica y carbonatada, son atribuidas aquí tanto a posibles cambios climáticos como a cambios en la composición del área fuente. Estos fueron inducidos por la evolución tectónica de los margenes de la cuenca.

Composition, nanostructure, and optical properties of silver and silver-copper lusters

Lusters are composite thin layers of coinage metal nanoparticles in glass displaying peculiar optical properties and obtained by a process involving ionic exchange, diffusion, and crystallization. In particular, the origin of the high reflectance (golden-shine) shown by those layers has been subject of some discussion. It has been attributed to either the presence of larger particles, thinner multiple layers or higher volume fraction of nanoparticles. The object of this paper is to clarify this for which a set of laboratory designed lusters are analysed by Rutherford backscattering spectroscopy, transmission electron microscopy, x-ray diffraction, and ultraviolet-visible spectroscopy. Model calculations and numerical simulations using the finite difference time domain method were also performed to evaluate the optical properties. Finally, the correlation between synthesis conditions, nanostructure, and optical properties is obtained for these materials.

Building complexity in O2-binding copper complexes : site-selective metalation and intermolecular O2-binding at dicopper and heterometallic complexes derived from an unsymmetric ligand

A novel unsymmetric dinucleating ligand (LN3N4) combining a tridentate and a tetradentate binding sites linked through a m-xylyl spacer was synthesized as ligand scaffold for preparing homo- and dimetallic complexes, where the two metal ions are bound in two different coordination environments. Site-selective binding of different metal ions is demonstrated. LN3N4 is able to discriminate between CuI and a complementary metal (M′ = CuI, ZnII, FeII, CuII, or GaIII) so that pure heterodimetallic complexes with a general formula [CuIM′(LN3N4)]n+ are synthesized. Reaction of the dicopper(I) complex [CuI 2(LN3N4)]2+ with O2 leads to the formation of two different copper-dioxygen (Cu2O2) intermolecular species (O and TP) between two copper atoms located in the same site from different complex molecules. Taking advantage of this feature, reaction of the heterodimetallic complexes [CuM′(LN3N4)]n+ with O2 at low temperature is used as a tool to determine the final position of the CuI center in the system because only one of the two Cu2O2 species is formed