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Molecular wire devices

Both conjugated polymer superlattices and porphyrin arrays connected with molecular wires device which are described here represent powerful candidates for optical and photonic materials. [Pg.474]

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]

Burtman V, Ndobe AS, Vardeny ZV (2005) Transport studies of isolated molecular wires in self-assembled monolayer devices. J Appl Phys 98(3) 034314-034319... [Pg.36]

Among the two-terminal devices that can be imagined for UE [capacitors, inductors, rectifiers, negative differential resistance (NDR) devices], the simplest is a molecular wire, that is, a molecule capable of conducting electricity a nanoconductor or, equivalently, a nanoresistor. Even the most conductive of molecular wires has a minimum resistance. [Pg.48]

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]

Abstract Described are the synthetic routes to precisely defined molecular wires which are of discrete length and constitution. They are fully conjugated systems and are expected to have nearly linear current-voltage response curves. Their ends are functionalized with molecular alligator clips, based on chalconides and isonitriles, for adhesion between proximal probes. Both solution and solid-phase approaches have been used to prepare these molecular wires that are based on oligofthiophene ethynylene)s and oligofphe-nylene ethynylene)s. Molecular device syntheses are also described that would be expected to have nonlinear current-voltage responses. [Pg.237]

Keywords Molecular Wires a Molecular Devices a Alligator Clips a Conjugated Materials... [Pg.237]

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]

Keywords Molecular Devices a Molecular Machines a Molecular Wires a Antenna Systems a Molecular Switches a Plug/socket Systems a Pseudorotaxanes a Rotaxanes a Catenanes a Supramolecuiar Chemistry a Photochemistry a Electrochemistry a Luminescence... [Pg.255]

Synthetic routes to precisely defined molecular wires and devices are described along with procedures for testing their electronic properties. [Pg.404]

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]


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