Aryl-substituted dithiafulvenes: synthesis, electronic properties, and redox reactivity
Author:
Funder
NSERC
CFI
RDC NL
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
1. Linearly extended π-donors: when tetrathiafulvalene meets conjugated oligomers and polymers
2. Synthesis and properties of novel tetrathiafulvalene vinylogues
3. Vinylogous Tetrathiafulvalene (TTF) π-Electron Donors and Derived Radical Cations: ESR Spectroscopic, Magnetic, and X-ray Structural Studies
4. A simple route to novel functionalized tetrathiafulvalene vinylogues
5. Tetrathiafulvalenes, Oligoacenenes, and Their Buckminsterfullerene Derivatives: The Brick and Mortar of Organic Electronics
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1. Donor–Acceptor Fluorophores and Macrocycles Built Upon Wedge-Shaped π-Extended Phenanthroimidazoles;The Journal of Organic Chemistry;2023-03-02
2. Studies of a bola-type bis(dithiafulvene) molecular system: synthesis, crystal structure, and electrochemical properties;New Journal of Chemistry;2022
3. 1,3-Dithioles;Comprehensive Heterocyclic Chemistry IV;2022
4. A Comparative Study of Redox-Active Dithiafulvenyl-Functionalized 1,3,6,8-Tetraphenylpyrene Derivatives;The Journal of Organic Chemistry;2021-09-07
5. Donor/acceptor substituted dithiafulvenes and tetrathiafulvalene vinylogues: electronic absorption, crystallographic, and computational analyses;New Journal of Chemistry;2021
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