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Conductors, molecular

R. T. Oakley, Chemical Binding Within and Between Inorganic Rings The Design and Synthesis of Molecular Conductors, Can. J. Chem., 71, 1775 (1993). [Pg.12]

The electrochemistry of S-N and Se-N heterocycles has been reviewed comprehensively. The emphasis is on the information that electrochemical studies provide about the redox properties of potential neutral conductors. To be useful as a molecular conductor the 4-1, 0, and -1 redox states should be accessible and the neutral radical should lie close to the centre of the redox spectrum. The chalcogen-nitrogen heterocycles that have been studied in most detail from this viewpoint... [Pg.42]

Dithiazolyl radicals have also attracted considerable attention recently as potential molecular conductors (Section 11.3.6). The advantage of these systems over 1,2,3,5-dithiadiazolyls lies in their relatively low disproportionation energies (Section 11.3.1). [Pg.67]

The coordination of redox-active ligands such as 1,2-bis-dithiolates, to the M03Q7 cluster unit, results in oxidation-active complexes in sharp contrast with the electrochemical behavior found for the [Mo3S7Br6] di-anion for which no oxidation process is observed by cyclic voltammetry in acetonitrile within the allowed solvent window [38]. The oxidation potentials are easily accessible and this property can be used to obtain a new family of single-component molecular conductors as will be presented in the next section. Upon reduction, [M03S7 (dithiolate)3] type-11 complexes transform into [Mo3S4(dithiolate)3] type-I dianions, as represented in Eq. (7). [Pg.114]

Molecular Conductors Based on M3Q7 Cluster Complexes... [Pg.115]

Carrier generators in molecular conductors have been associated for a long time to a partial charge transfer between the HOMO (or LUMO) electronic band and other chemical species. These systems are known as two-component molecular conductors. Tetrathiofulvalene derivatives are versatile systems for the formation of molecular organic conductors due to their electron donor capacity by transferring one u-electron from the HOMO orbital, and to their planar shape that promotes their stacking as a consequence of the n-n orbital overlap. The electronic properties of these salts are essentially determined by the packing pattern of the donor molecules which, in turn, depends on the counter-ion. [Pg.115]

At the turn of this century it was realized that carrier generation was also possible between the HOMO and LUMO band even in neutral single-component materials assuming that there was a small HOMO-LUMO gap and conduction paths have been associated with the presence of large transverse intermolecular interactions. The most relevant examples of single-component molecular conductors are the mononuclear M(dithiolate)2 (M = Co, Ni, Cu, Au) complexes with... [Pg.115]

As described most elegantly elsewhere in this volume, the halogen bond is an intermolecular, charge-transfer interaction between a Lewis base and an electron-deficient halogen. Other chapters that accompany this chart its use in, for example, supramolecular chemistry, molecular conductors and coordination chemistry. In this chapter, a much more recent application of halogen bonding is described, namely in the realisation of liquid-crystalline materials. [Pg.171]

Batail P (ed) (2004) Thematic Issue on Molecular Conductors. Chem Rev 104(11)... [Pg.215]

C. Coulon and R. Clerac, Electron spin resonance A major probe of molecular conductors, Chem. Rev., 2004, 104, 5655. [Pg.164]

In this section, we look more closely at what effect the chalcogen atom has on the properties of the molecular conductors we describe. We do not attempt to review exhaustively all the chalcogen-containing components in electroactive systems, to do so would be a colossal task. Instead, carefully chosen examples and studies illustrate how chalcogen chemistry is used in the design and manipulation of electroactive materials, and ultimately how it effects suitability for molecular device applications. [Pg.773]

Other common techniques have been applied to the assembly of layers or films of TTF-derived molecular conductors. Compound 29 is an example of an amphiphilic TTF derivative. It forms conducting Langmuir-Blodgett charge transfer films with the acceptor TCNQF4 (30).98 Self-assembly of compound 31 on gold by electrochemical methods yielded an electroactive monolayer which was remarkably stable to electrochemical cycling.99... [Pg.778]

Keywords Cation-radical salts, Molecular conductors, Organic superconductors, Organometallic anions, Tetrakis(trifluoromethyl)metallates, Tetrathiafulvalene... [Pg.2]

The synthesis of the bis-l,3-dithiolium radical cation (TTF+) in 1970 [1] enabled dramatic growth in the field of molecular conductors in the decades thereafter. TTF and several of its homologues are depicted in Scheme 1. The field of low dimensional molecular metals was further motivated by the discovery of the TTF-TCNQ charge-transfer complex in 1973 [2, 3]. Seven years later, superconductivity was induced in the cation-radical salt, (TMTSF)2PF6, upon application of 12 kbar pressure [4]. Shortly thereafter, superconductivity below 1.4 K was observed at ambient pressure in the perchlorate analog [5]. [Pg.4]

Keywords Donor type metal complexes, Metal dithiolene complexes, Molecular conductors, Organometallic complexes, Unsymmetrical metal complexes... [Pg.35]

Molecular Conductors Based on Cationic Metal Complexes. 40... [Pg.35]

General Introduction of Molecular Conductors 1.1 General Features of Molecular Conductors... [Pg.37]

Since the discovery of the first organic semiconductor perylene-bromine complex in 1954 [1], a large number of molecular conductors, including more than 100 molecular superconductors, have been prepared. Conducting molecular materials are characterized by the following features ... [Pg.37]

Thanks to these characteristics, the molecular conductor is now one of the standard materials in condensed matter physics and interdisciplinary basic science is expanding. [Pg.37]


See other pages where Conductors, molecular is mentioned: [Pg.585]    [Pg.703]    [Pg.839]    [Pg.848]    [Pg.68]    [Pg.217]    [Pg.106]    [Pg.116]    [Pg.125]    [Pg.192]    [Pg.192]    [Pg.210]    [Pg.339]    [Pg.916]    [Pg.179]    [Pg.738]    [Pg.758]    [Pg.763]    [Pg.814]    [Pg.890]    [Pg.30]    [Pg.31]    [Pg.35]    [Pg.35]    [Pg.35]    [Pg.35]    [Pg.36]    [Pg.37]   
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Molecular Inorganic Conductors and Superconductors

Molecular conductors complexes

Molecular conductors fabrication

Molecular conductors nanowires

Molecular conductors organic

Molecular conductors single-component

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Molecular dynamics conductors

Why Enantiopure Molecular Conductors

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