Tetracyanoquinodimethane metal

Espinosa, E., Molins, E. and Lecomte, C. (1997), Electron density study of the one dimensional organic metal bis(thiodimethylene)-tetrathiofulvalene tetracyanoquinodimethane, Phys. Rev. B, 56(4), 1820-1833. 

Another synthesis of olefins has been described in which the desulphurization of thiirans by triphenylphosphine is featured.72 There have been many reports of the synthesis of compounds of the type (63). These form charge-transfer complexes with acceptors such as tetracyanoquinodimethane which have metallic properties. The... 

Figure 3.18. Thin TTF-TCNQ film (thickness 1 um) HV-grown on a KCl(lOO) substrate, (a) Topography and (b) amplitude TMAFM images. The scale is 5 p.m x 5 ]xm. (c) FTIR spectra of the CN stretching mode in neutral TCNQ (powder) and in a TTF-TCNQ thin film (thickness 1 um) HV-grown on KBr(lOO). Reprinted from Surface Science, Vol. 482 85, C. Rojas, J. Caro, M. Grioni and J. Fraxedas, Surface characterization of metallic molecular organic thin films tetrathiaful-valene tetracyanoquinodimethane, 546-551, Copyright (2001), with permission from Elsevier.

Through reduction or oxidation of the molecule by a dopant molecule. Atoms or molecules with high electron affinity, such as iodine, antimony pentafluoride (SbCls), or 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4-TCNQ), may oxidize a typical organic semiconductor such as poly(p-phenylene) derivatives, leaving them positively charged. Reduction, i.e., addition of an electron, may be obtained by doping with alkali metals. 

In the case of the trinuclear [ t-N1,C2-bzimAu]3 (bzim = benzylimidazolate), in addition to the extended structures that form with other metals (see Section 6.3), it also forms supramolecular networks, acting as an electron donor with small organic acids [48]. For example, it reacts with TCNQ (tetracyanoquinodimethane) giving rise to a columnar structure in which each TCNQ molecule is sandwiched between two units of the trinuclear complex in a face-to-face manner. Thus, the repetition of this pattern leads to a stacking of the type (Au3)(Au3)( t-TCNQ)(Au3)... 

Furan analogs of tetracyanoquinodimethane as new organic metals 92MI23. 

J. B. Torrance, Spin waves, scattering at 4kFr and spin-Peierls fuctuations in an organic metal Tetrathiafulvalene-tetracyanoquinodimethane (TTF-TCNQ), Phys. Rev. B17 3099-3103 (1978). 

J. B. Torrance, The difference between metallic and insulating salts of tetracyanoquinodimethane (TCNQ) How to design an organic metal, Acc. Chem. Res. 12 79-86 (1979). 

M. Mizuno, A. F. Garito, and M. P. Cava, Organic metal Alkylthio substitution effects in tetrathiafulvalene-tetracyanoquinodimethane charge transfer complexes, J. Chem. Soc. Chem. Commun. 18-19 (1978). 

Tetracyanoquinodimethane (TCNQ) and many of its derivatives are easily reduced to anions of the type TCNQ-, which form salts with various cations. With many cations, e.g., tetrathiafulvalene cations (TTF+), and N-methyl phenazinium cations (NMP+), the TCNQ- anions form electronically conducting salts (- molecular metals, -> charge-transfer complexes) that can be used as electrodes, especially because of their electrocatalytic properties (- biosensors, -> electrocatalysis, -> molecular metals) [i,ii]. TCNQ undergoes insertion electrochemical reactions (-> insertion electrochemistry) leading to TCNQ salts [iii, iv]. Polymers... 

Tetrathiafulvalene electrodes — Tetrathiafulvalene (TTF) and many of its derivatives are easily oxidized to form cations of the type TTF+. With various anions, most prominent is the tetracyanoquinodimethane anion (TCNQ-), these cations form - charge-transfer complexes, i.e., salts with metal-like conductivities (- molecular metals). These salts are used in electrochemistry as electrodes or to modify the surface of electrodes, for the purpose of achieving desirable electrocatalytic properties (- electrocatalysis). Tetrathiafulvalene-substituted polystyrenes have also been synthesized and used as modified electrodes [ii]. 

Metal-vapour-deposition methods have begun to provide new low-valent complexes of uncommon stoichiometry. The preparation of gram quantities of paramagnetic (ji = 2.02 BM) [Co(bipy)2] has been reported and its reactions with Br2, tetracyanoethylene and tetracyanoquinodimethane studied.283 Electrochemically it behaves identically to [Co(bipy)3]2+ (equation 47).283... 

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