4.8 Article

Straightforward access to aryl-substituted tetrathiafulvalenes by palladium-catalysed direct C-H arylation and their photophysical and electrochemical properties

Journal

CHEMICAL SCIENCE
Volume 2, Issue 10, Pages 2017-2021

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1sc00372k

Keywords

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Funding

  1. MEXT
  2. JSPS
  3. Kinki Invention Center
  4. [22245006]
  5. [20108006]
  6. [22106523]
  7. Grants-in-Aid for Scientific Research [22106523, 23655034, 20108001, 20108006, 22245006] Funding Source: KAKEN

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Treatment of tetrathiafulvalene (TTF) with aryl bromides in the presence of cesium carbonate and a palladium catalyst results in direct arylation of TTF. The direct arylation is inherently straightforward and efficient, hence easily creating a large library of aryl TTFs for systematic investigations of structure-property relationships. The present protocol will thus represent an efficient method for exploiting TTF-based interesting functional materials.

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