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Applications molecular wires

Many other opportunities exist due to the enormous flexibility of the preparative method, and the ability to incorporate many different species. Very recently, a great deal of work has been published concerning methods of producing these materials with specific physical forms, such as spheres, discs and fibres. Such possibilities will pave the way to new application areas such as molecular wires, where the silica fibre acts as an insulator, and the inside of the pore is filled with a metal or indeed a conducting polymer, such that nanoscale wires and electronic devices can be fabricated. Initial work on the production of highly porous electrodes has already been successfully carried out, and the extension to uni-directional bundles of wires will no doubt soon follow. [Pg.73]

As a class of n-type organic semiconductors, PBI derivatives have received considerable attention for a variety of applications [312, 313], for example, for organic or polymer light-emitting diodes (OLEDs and PLEDs) [314, 315], thin-film organic field-effect transistors (OFETs) [316, 317], solar cells [318, 319], and liquid crystals [320]. They are also interesting candidates for single-molecule device applications, such as sensors [321], molecular wires [322], or transistors [141]. [Pg.166]

One of the first applications of the new mesh and node intramolecular circuit rules discussed above is the well-known problem in electrical circuit theory of the balancing of a Wheatstone bridge. In Fig. 21, a molecular Wheatstone bridge is presented, made of loop-like 4 tolane molecular wires bonded via benzopyrene end-groups for nano-pads 1 and 3, and via pyrene end-groups for nano-pads 2 and 4. This four-electrode and four-branch molecule is connected to a battery and an ammeter. [Pg.247]

Mujica V, Kemp M, Ratner M (1994) Electron conduction in molecular wires. H Application to scanning tunneling microscopy. J Chem Phys 101 6856... [Pg.263]

The use of molecular wires and devices for electronics applications is destined to occur. The ability to control molecular structures at the subnanometer scale is obvious throughout chemical synthesis. These are the same techniques that have been optimized over the last 50 years for the synthesis and modification of compounds for pharmaceutical, dye, petroleum, and fine chemical indus-... [Pg.250]

Before examining the electrochemical properties of this class of compounds (we will limit the discussion to homonuclear derivatives), it must be clear that the technological application of molecular wires belongs to solid-state chemistry. Nevertheless, since the main target of such new molecules is to conduct electricity, it seems useful to ascertain preliminarily their intrinsic ability towards intramolecular electron mobility by electrochemical investigations in solution, i.e. in the absence of intermolecular interactions. [Pg.519]

The use of Molecular Wires in Electrochemistry such that Long-Distance Electron Transfer can be Exploited for a Variety of Applications... [Pg.35]

The final aspect of the electrode design in the work by Hess et al. [118] is the use of molecular wires for modified electrodes for applications other than molecular... [Pg.35]

These types of switchable electrode surfaces have been used to selectively pattern two different cell populations onto a surface [151] and additionally these surfaces can selectively release different cells at different applied potentials [152]. However, it is important to recognize that electrochemically switching a surface from inactive to conjugation and active to conjugation has been well explored with nitro-terminated aryl diazonium salts. In such studies, the application where very anodic potential resulted in a six-electron reduction to an amine [139], to which proteins could be attached [153-155]. The key difference is that the interaction of the biological medium with the surface is controlled by the presence of the antifouling layer. In many ways these electrode surfaces developed by Mrksich and coworkers [150-152, 156] are very similar to the antifouling surfaces with molecular wires discussed in Section 1.4.2 [131, 132, 138, 142]. In both cases the electrode is... [Pg.42]

After the discovery by Fischer and Maasbol of the first stable carbene complexes in 1964, i.e., [(CO)5W =C(OMe)R ] [21], generation of related metaUacumulene derivatives [M]=C(=C) =CR2 (n > 0) was obviously envisaged. Thus, it is presently well-established that stabilization of these neutral unsaturated carbenes by coordination to a transition metal center is possible by the use of the lone pair of electrons on the carbenic carbon atom, via formation of a metal-carbon a-bond (electron back-donation from the metal fragment to the carbon ligand may strengthen this bond). This has allowed the development of a rich chemistry of current intense interest due to the potential applications of the resulting metallacumulenic species in organic synthesis, as well as in the construction of molecular wires and other nanoelectronic devices [22]. [Pg.153]

The covalent chemistry of fullerenes has developed very rapidly in the past decade in an effort to modify fuUerene properties for a number of applications such as photovoltaic cells, infrared detectors, optical limiting devices, chemical gas sensors, three-dimensional electroactive polymers, and molecular wires [8, 25, 26, 80-82]. Systematic studies of the redox properties of Cgo derivatives have played a crucial role in the characterization of their unique electronic properties, which lie at the center of these potential applications. Furthermore, electrochemical techniques have been used to synthesize and separate new fullerene derivatives and their isomers as well as to prepare fullerene containing thin films and polymers. In this section, to facilitate discussion of their redox properties, Cgo derivatives have been classified in three groups on the basis of the type of attachment of the addend to the fullerene. In group one, the addends are attached via single bonds to the Cgo surface as shown in Fig. 6(a) and are referred to as singly bonded functionalized derivatives. The group includes... [Pg.159]

An interesting futuristic application is in the field of molecular electronics where a one-dimensional molecular wire such as polyacetylene in combination with a suitable molecular switch, e.g. salicylideneanilines, would yield a molecular microchip whose information storage capacity would be about 10 times that of a conventional microchip. A new generation of high performance computer with memory elements of nanometre dimensions is visualized on the basis of such molecular microchips. [Pg.461]

The formation of carbon-carbon cross-links is by far the most important effect and is the basis of the applications in wire and cable industry and for heat-shrinkable products. The factors affecting the changes of polyethylene by irradiation are the molecular weight distribution, branching, degree of unsaturation, and morphology. °... [Pg.96]

Due to the relative ease of carrying out the reaction and the versatility of the process, the hydrosilylation reaction has been used in a number of interesting extensions and applications. Here several of them are highlighted. In one report, Lop-inski and coworkers used the same concept of the radical-initiated hydrosilylation reaction on the Si(100)-2 x 1 surface to induce self-directed growth of molecular wires on the surface [141]. On the Si(100)-2 x 1 surface, the radical chain reaction propagates primarily along the direction of the dimer row, leading to lines of... [Pg.341]

New boxed applications include an arsenic biosensor (Chapter 0). microcantilevers to measure attograms of mass (Chapter 2), molecular wire (Chapter 14), a fluorescence resonance energy transfer biosensor (Chapter 19), cavity ring-down spectroscopy for ulcer diagnosis (Chapter 20), and environmental mercury analysis by atomic fluorescence (Chapter 21). [Pg.793]

Thienyl derivatives hexarylethane unit 359 has been prepared for molecular wires applications (04OL2523). [Pg.243]

Molecular electronics - the long, fibrillar nature of gels strongly suggests that they might find applications in the construction of molecular wires. [Pg.922]

Time-Local Quantum Master Equations and their Applications to Dissipative Dynamics and Molecular Wires... [Pg.339]


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See also in sourсe #XX -- [ Pg.729 ]

See also in sourсe #XX -- [ Pg.838 ]

See also in sourсe #XX -- [ Pg.921 ]




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Molecular applications

Molecular wires

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