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  Tetrathiafulvalenoparacyclophanes

Staab, H. A., Ippen, J., Tao‐pen, C., Krieger, C., & Starker, B. (1980). Tetrathiafulvalenoparacyclophanes. Angewandte Chemie International Edition, 19(1), 66-67. doi:10.1002/anie.198000661.

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AngewChemIntEd_19_1980_66.pdf (Any fulltext), 239KB
 
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 Creators:
Staab, Heinz A.1, Author           
Ippen, Joachim2, Author           
Tao‐pen, Chu2, Author           
Krieger, Claus1, Author           
Starker, Barbara1, Author           
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1Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society, ou_1497706              
2Max Planck Institute for Medical Research, Max Planck Society, ou_1125545              

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 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).

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Language(s): eng - English
 Dates: 1979-08-132003-12-221980-01
 Publication Status: Issued
 Pages: 2
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 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.198000661
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Title: Angewandte Chemie International Edition
  Abbreviation : Angew. Chem. Int. Ed.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 19 (1) Sequence Number: - Start / End Page: 66 - 67 Identifier: ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851