Transition nanoparticles

Bray KL (2001) High Pressure Probes of Electronic Structure and Luminescence Properties of Transition Metal and Lanthanide Systems. 213 1-94 Bronstein LM (2003) Nanoparticles Made in Mesoporous Solids. 226 55-89 Bronstrup M (2003) High Throughput Mass Spectrometry for Compound Characterization in Drug Discovery. 225 275-294... 

Recent advances of the Seeman group led to the construction of a nanomechanical device from DNA [89]. In this molecular apparatus, the ion-dependent transition of B-DNA into the Z-conformation is used to alter the distance between two DNA DX domains attached to the switchable double helix. Atomic displacements of about 2-6 nm were attained. Ionic switching of nanoparticles by means of DNA supercoiling has also been reported [53]. Additional advances regarding the use of DNA is nanomechanical devices have been reported by Fritz et al., who showed that an array of cantilevers can be used to... 

Although random and irregular type GaN nanorods have been prepared by using transition metal nanoparticles, such as Ni, Co, and Fe as catalysts and carbon nanotubes as the template, the preparation of controllable regular array of strai t GaN nanorods has not yet been reported. Fabrication of well-ordered nano-structures with high density is very important for the application of nano-structures to practical devices. 

The application of ly transition metal carbides as effective substitutes for the more expensive noble metals in a variety of reactions has hem demonstrated in several studies [ 1 -2]. Conventional pr aration route via high temperature (>1200K) oxide carburization using methane is, however, poorly understood. This study deals with the synthesis of supported tungsten carbide nanoparticles via the relatively low-tempoatine propane carburization of the precursor metal sulphide, hi order to optimize the carbide catalyst propertira at the molecular level, we have undertaken a detailed examination of hotii solid-state carburization conditions and gas phase kinetics so as to understand the connectivity between plmse kinetic parametera and catalytically-important intrinsic attributes of the nanoparticle catalyst system. 

Binary systems of ruthenium sulfide or selenide nanoparticles (RujcSy, RujcSey) are considered as the state-of-the-art ORR electrocatalysts in the class of non-Chevrel amorphous transition metal chalcogenides. Notably, in contrast to pyrite-type MS2 varieties (typically RUS2) utilized in industrial catalysis as effective cathodes for the molecular oxygen reduction in acid medium, these Ru-based cluster materials exhibit a fairly robust activity even in high methanol content environments of fuel cells. 

Finally, the term steric stabihzation coifid be used to describe protective transition-metal colloids with traditional ligands or solvents [38]. This stabilization occurs by (i) the strong coordination of various metal nanoparticles with ligands such as phosphines [48-51], thiols [52-55], amines [54,56-58], oxazolines [59] or carbon monoxide [51] (ii) weak interactions with solvents such as tetrahydrofuran or various alcohols. Several examples are known with Ru, Ft and Rh nanoparticles [51,60-63]. In a few cases, it has been estab-hshed that a coordinated solvent such as heptanol is present at the surface and acts as a weakly coordinating ligand [61]. 

In summary, Dupont and coworkers have developed an organometalhc approach for the stabihzation of various zero-valent nanoparticles in the ionic liquid BMI PPe. Transition metal nanoparticles of 2.0-3.0 were obtained with... 

As judiciously reported by the authors, the yields are too low for technical appUcations but this reaction represents the second example of partial hydrogenation of monocyclic arene by soluble transition metal nanoparticles. 

Mixtures of a nematic liquid crystal (LC or LC ) with small quantities of gold nanoparticles coated with alkylthiolates (<5 wt%) including an alkylthiolate functionalized with a chiral group have been studied (Figure 8.29) [72]. All mixtures show nematic mesophases with transition temperatures and phase stability very similar to those oftheliquid crystal precursors LC or LC. The introduction ofachiral center into the mixtures (mixtures of Au ) produce chiral nematic mesophases. A similar result is obtained in mixtures of Au and LC doped with the chiral dopant (s)-Naproxen. 

The results discussed in Sections 3.1-3.3 turned out as very valuable with respect to the knowledge about the transition from bulk metal to molecule. The most important method, however, to gain direct information from individual metal nanoparticles on their inner electronic life is the tunnelling spectroscopy. The method is based on the single-electron tunnelling (SET) through an intermediate island between two metal electrodes as is indicated in Figure 10. 

It should be mentioned here that Finke s group has added a whole plethora of significant contributions to the field of metal nanoclusters [295-299] including a recent study on the mechanism for the self-assembly of transition metal nanoparticles [294]. 

Finke has reported remarkable catalytic lifetimes for the polyoxoanion- and tetrabutylammonium-stabi-lized transition metal nanoclusters [288-292]. For example in the catalytic hydrogenation of cyclohexene, a common test for structure insensitive reactions, the lr(0) nanocluster [296] showed up to 18,000 total turnovers with turnover frequencies of 3200 h [293]. As many as 190,000 turnovers were reported in the case of the Rh(0) analogue reported recently. Obviously, the polyoxoanion component prevents the precious metal nanoparticles from aggregating so that the active metals exhibit a high surface area [297]. 

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