499 research outputs found
Tunneling anisotropic magnetoresistance in organic spin valves
We report the observation of tunneling anisotropic magnetoresistance (TAMR)
in an organic spin-valve-like structure with only one ferromagnetic electrode.
The device is based on a new high mobility perylene diimide-based n-type
organic semiconductor. The effect originates from the tunneling injection from
the LSMO contact and can thus occur even for organic layers which are too thick
to support the assumption of tunneling through the layer. Magnetoresistance
measurements show a clear spin-valve signal, with the typical two step
switching pattern caused by the magnetocrystalline anisotropy of the epitaxial
magnetic electrode.Comment: 10 pages 5 figures Paper has been rewritten, new results have been
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Efficient Electrochemical Water Oxidation by a Trinuclear Ru(bda) Macrocycle Immobilized on Multi-Walled Carbon Nanotube Electrodes
G-arylated hydrogen-bonded cyclic tetramer assemblies with remarkable thermodynamic and kinetic stability
The preparation and self-assembly of novel G-C dinucleoside monomers that are equipped with electron-poor aryl groups at the G-N2 amino group have been studied. Such monomers associate via Watson-Crick H-bonding into discrete unstrained tetrameric macrocycles that arise as a thermodynamically and kinetically stabilized product in a wide variety of experimental conditions, including very polar solvent environments and low concentrations. G-arylation produces an increased stability of the cyclic assembly, as a result of a subtle interplay between enthalpic and entropic effects involving the solvent coordination sphereFunding from the European Research Council (ERC-StG 279548) and MINECO (CTQ2011-23659) is gratefully acknowledge
Emergence of light-driven protometabolism on recruitment of a photocatalytic cofactor by a self-replicator
Establishing how life can emerge from inanimate matter is among the grand challenges of contemporary science. Chemical systems that capture life’s essential characteristics—replication, metabolism and compartmentalization—offer a route to understanding this momentous process. The synthesis of life, whether based on canonical biomolecules or fully synthetic molecules, requires the functional integration of these three characteristics. Here we show how a system of fully synthetic self-replicating molecules, on recruiting a cofactor, acquires the ability to transform thiols in its environment into disulfide precursors from which the molecules can replicate. The binding of replicator and cofactor enhances the activity of the latter in oxidizing thiols into disulfides through photoredox catalysis and thereby accelerates replication by increasing the availability of the disulfide precursors. This positive feedback marks the emergence of light-driven protometabolism in a system that bears no resemblance to canonical biochemistry and constitutes a major step towards the highly challenging aim of creating a new and completely synthetic form of life. [Figure not available: see fulltext.]
Molecular aspects of squaraine dyes aggregation and its influence on spectroscopic properties
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