Synthesis of 2,3-dimethylthio-6-pyridyl tetrathiafulvalene: a precursor for a new system involving a direct linkage between a strong donor (D) and a strong acceptor (A)-Reference-Cited by-同舟云学术

Synthesis of 2,3-dimethylthio-6-pyridyl tetrathiafulvalene: a precursor for a new system involving a direct linkage between a strong donor (D) and a strong acceptor (A)

Published:2001-02 Issue:8 Volume:42 Page:1571-1573
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Paz-Tal Levi Ofra,Becker James Y,Ellern Arkady,Khodorkovsky Vladimir

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Tetrathiafulvalenes as π-Electron Donors for Intramolecular Charge-Transfer Materials

2. Synthesis of a novel rigid tetrathiafulvalene-σ-p-benzoquinone diad (TTF-σ-Q) with inherent structural configuration suitable for intramolecular charge-transfer

3. TTF-NHCO2(CH2)2 O-TCNQBr and TTF-Co2(Ch2)2 O-TCNQBR, Two Potential Molecular Rectifiers

4. Semiconducting Langmuir–Blodgett films of non-amphiphilic ethylenedithio–tetrathiafulvalene derivatives bearing pyridine and pyridinium substituents

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