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Electron donor‐acceptor compounds, 45 syntheses of [2.2]‐, [3.3]‐, and [4.4]Paracyclophanes with 1,2,4,5‐Tetracyanobenzene units as electron acceptors

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

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Wahl,  Peter
Max Planck Institute for Medical Research, Max Planck Society;

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Kay,  Kwang-Yol
Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Staab, H. A., Wahl, P., & Kay, K.-Y. (1987). Electron donor‐acceptor compounds, 45 syntheses of [2.2]‐, [3.3]‐, and [4.4]Paracyclophanes with 1,2,4,5‐Tetracyanobenzene units as electron acceptors. Chemische Berichte, 120(4), 541-549. doi:10.1002/cber.19871200414.


Cite as: https://hdl.handle.net/21.11116/0000-0007-9C5F-0
Abstract
[2.2]Paracyclophanes 1–4 containing tetracyanobenzene (TCNB) units opposite to different electron donor components have been synthesized via the corresponding substituted dithia[3.3]paracyclophanes 8, 10, 12, and 14. For the pyrolysis of the disulfones 9, 11, 13, and 15 derived therefrom, due to the very low volatility of these compounds, a modification of the conventional pyrolysis method had to be used. – The syntheses of [3.3]paracyclophanes 16–18 via the dithia[4.4]paracyclophanes 19, 21, and 23 and the corresponding disulfones 20, 22, and 24 are described. [4.4]Paracyclophanes 32 and 33 were prepared from the respective dithia[5.5]paracyclophanes 34 and 36 by pyrolysis of the disulfones 35 and 37. – As cyclisation components for the synthesis of the mentioned dithiaparacyclophanes several new 1,4‐bis(mercaptoalkyl)benzenes with electron‐donating substituents were prepared as was the TCNB derivative 5.