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[2.2]‐ and [3.3]Tetrathiafulvalenophanes

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Starker,  Barbara
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

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Schweitzer,  Dieter
Department of Molecular Physics, Max Planck Institute for Medical Research, Max Planck Society;

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Staab,  Heinz A.
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Ippen, D. J., Tao‐pen, C., Starker, B., Schweitzer, D., & Staab, H. A. (1980). [2.2]‐ and [3.3]Tetrathiafulvalenophanes. Angewandte Chemie, International Edition, 19(1), 67-69. doi:10.1002/anie.198000671.


Cite as: https://hdl.handle.net/21.11116/0000-0004-9655-3
Abstract
In the “metallic” conducting 1:1 complex of tetrathiafulvalene (TTF) and tetracyanoquinodimethane (TCNQ), donor and acceptor molecules form separate stacks in the crystal. In order to enforce other TTF/TCNQ arrangements by altering the molecular architecture the phane‐like bridged TTF‐paracyclophanes (1), n = 3, and (2) were first synthesized. To do this a novel reaction sequence had to be developed which also facilitated synthesis of the tetrathiafulvalenophanes (3)/(4) (and the corresponding [2.2]‐derivatives). (3)/(4) and TCNQ form a 1:4 complex having a conductivity of σ = 5 × 10−3 to 10−2 [Ω cm]−1 (single crystal, long axis, 300 K).