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TTF

Figure C 1.2.9. Schematic representation of photo induced electron transfer events in fullerene based donor-acceptor arrays (i) from a TTF donor moiety to a singlet excited fullerene and (ii) from a mthenium excited MLCT state to the ground state fullerene. Figure C 1.2.9. Schematic representation of photo induced electron transfer events in fullerene based donor-acceptor arrays (i) from a TTF donor moiety to a singlet excited fullerene and (ii) from a mthenium excited MLCT state to the ground state fullerene.
Llacay J, Veciana J, Vidal-Gancedo J, Bourdelande J L, Gonzalez-Moreno R and Rovira C 1998 Persistent and transient open-shell species derived from Cgg-TTF cyclohexane-fused dyads J. Org. Chem. 63 5201-10... [Pg.2435]

The highly conductive class of soHds based on TTF—TCNQ have less than complete charge transfer (- 0.6 electrons/unit for TTF—TCNQ) and display metallic behavior above a certain temperature. However, these soHds undergo a metal-to-insulator transition and behave as organic semiconductors at lower temperatures. The change from a metallic to semiconducting state in these chain-like one-dimensional (ID) systems is a result of a Peieds instabihty. Although for tme one-dimensional systems this transition should take place at 0 Kelvin, interchain interactions lead to effective non-ID behavior and inhibit the onset of the transition (6). [Pg.239]

The temperature of the metal-to-insulator transition in TTF—TCNQ is 53 K. For systems with increased interchain coupling, the transition temperature for the onset of metallic conduction increases roughly as the square of the interaction between the chains. This behavior is tme as long as the coupling between chains remains relatively weak. For compounds with strong interactions between stacks, the material loses its quasi-ID behavior. Thus, the Peieds distortion does not occur even at low temperatures, and the materials remain conductive. [Pg.239]

Fig. 4. Orbital overlap for conduction molecular orbitals and molecular stacking in tetrathiafulvalene (TTF). Fig. 4. Orbital overlap for conduction molecular orbitals and molecular stacking in tetrathiafulvalene (TTF).
A large family of compounds is based on combination of TTF-type donors and TCNQ-type acceptors. The resulting solids form... [Pg.241]

One may consider a factor of safety of. id-100%, depending upon the criticality ttf the installation in all the forces that may arise on an actual fault to ensure a foolproof system. [Pg.905]

Chemical Reactivity - Reactivity with Water No reaction Reactivity with Common Materials No reaction Stability During Transport Stable Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Not pertinent Inhibitor ttf Polymerization Not pertinent. [Pg.168]

The structures of the black crystalline benzene solvate C6o-4C6H6, the black charge-transfer complex with bis(ethylenedithio)tetrathiafulvene, [C6o(BEDT-TTF)2], and the black ferrocene adduct [C6o Fe(Cp)2)2] (Fig. 8.7b) ) have also been solved and all feature the packing of Cso clusters. [Pg.282]

Certain abbreviations are used in the article for compounds that are mentioned repeatedly. Tlius, TTF is tetrathiafulvalene, TCNQ is tetracyanoquin-odimethane, TTDAF is tetrathiadiazafulvalene, DTDAF is dithiadiazafulva-lene, and TAF is tetraazafulvalene. [Pg.118]

Tlie interest in the preparation and use of dithiolium salts in connection with the synthesis of TTF derivatives led to the development of a new uses of heteroaromatic cations in organic synthesis. Based on that, a new carbonyl olefination for the synthesis of numerous heterofulvalenes was developed (77S861). For example, 2-dimethoxyphosphinyl-l,3-benzodithiole was deprotonated with butyllithium in THF at -78°C and the resulting phosphonate carbanion reacted with 9-alkyl-acridones to give the dithia-azafulvalenes of type 45 (78BCJ2674) (Scheme 15). [Pg.125]

In contrast to the intensively examined tetrathiafulvalenes (TTFs), which are of interest in the field of material science, the TAFs have been less well... [Pg.137]

Tire deprotonation of thiazolium salts (see Section II) under argon at room temperature allowed the characterization of nonfused DTDAF of types 52 and 53 by cyclic voltammetry. Their very good donor properties were confirmed by two quasi-reversible peaks of equal intensity (93CC601). It is noteworthy that upon a second scan the first oxidation peak was shifted from -0.03 to -0.04 V. Upon further scans the voltam-mogram remains unchanged. Tliis interesting feature has been observed previously with TTF analogs. It was demonstrated that the neutral form... [Pg.158]


See other pages where TTF is mentioned: [Pg.1566]    [Pg.2422]    [Pg.618]    [Pg.624]    [Pg.190]    [Pg.224]    [Pg.979]    [Pg.1029]    [Pg.201]    [Pg.208]    [Pg.208]    [Pg.237]    [Pg.237]    [Pg.238]    [Pg.239]    [Pg.17]    [Pg.482]    [Pg.144]    [Pg.158]    [Pg.405]    [Pg.579]    [Pg.17]    [Pg.9]    [Pg.255]    [Pg.407]    [Pg.274]    [Pg.188]    [Pg.838]    [Pg.119]    [Pg.133]    [Pg.149]    [Pg.156]    [Pg.156]    [Pg.159]    [Pg.160]    [Pg.161]    [Pg.161]    [Pg.174]   
See also in sourсe #XX -- [ Pg.591 ]

See also in sourсe #XX -- [ Pg.477 ]

See also in sourсe #XX -- [ Pg.75 , Pg.130 ]




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5-cyanoisothiazolo-bis -TTF

A -TTF[Pd

A BEDT-TTF)

Ab Initio Calculation of Infinite TCNQ and TTF Stacks

Annulenoid TTFs

BEDO-TTF

BEDS-TTF

BEDT-TTF

BEDT-TTF complex

BEDT-TTF derivatives

BET-TTF

BPDT-TTF

Bi-TTF

Bis TTFs

Charge-transfer complex of TTF

Chiral TTFs

Cross-Conjugation and Electronic Structure in TTF Analogs

DT-TTF

Dendralene-type TTF analogs

Dimethylpyrazino- -TTF

Dimethylpyrazino-bis -TTF

EDS-TTF

EDT-TTF

EDT-TTF-COOH

Ethylenediselenolo-TTF

Ethylenediselenolo-TTF fulvalene

Extended TTF system

Isothiazolo-bis -TTF

K BEDT-TTF)

Methylenediselenolo-TTF

Methylenedithiolo-TTF

Multi-TTFs

Oxa-8-(4-Tetrathiafulvalenyl)Octyl-2,2-Bithiophene (PT-TTF)

Propylenediselenolo-TTF

Propylenedithiolo-TTF

Pyrazino- TTF

Pyrazino-bis -TTF

Pyridino-bis -TTF

Radialene-type TTF analogs

Stacks of TCNQ and TTF Molecules

Synthesis of FeOCl(TTF)

TCNQ and TTF Stacks

TCNQ-TTF system

TTF and derivatives

TTF crystal structure

TTF halides

TTF salts

TTF stacks

TTF structure

TTF structure classification

TTF units

TTF-C-BHTCNQ

TTF-TCNQ

TTF-TCNQ composites

TTF-crown ethers

TTF-dithiolate complexes

TTF-dithiolate ligands

TTFs in Cross-Conjugated Systems

TTFs salts

Tetrathiafulvalene (TTF)-Derived Dithiolenes

Tetrathiofulvalene tetracyanoquinodimethane TTF-TCNQ)

Thyroid transcription factor-1 (TTF

Tris-Fused TTF Analogs Possessing Dendralene Moieties

Tris-fused TTF analogs

Vinylenedithiolo-TTF

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