ScholarLens Back to search
2002•Journal of Heterocyclic ChemistryRequires access

Synthesis and electrochemical studies of tetrathiafulvalene derivatives (TTFs) as redox active ligands

Abd El‐Wareth A. O. Sarhan, Makoto Murakami, Taeko Izumi

Open publisher page 13 citations

Abstract

Abstract A simple route for synthesis of new tetrathiafulvalene dimethyl ester (TTF‐DME) is reported. The tetrathifulvalene dimethylester (TTF‐DME) has been prepared by introducing an ester coordination function as a bifunctional new donor. The redox behavior of the TTF‐DME was investigated in comparison to the well‐known dibenzotetrathiafulvene (DB‐TTF) by cyclic voltammetry. A two‐electron redox behavior was observed as a two waves.

About this research paper

What this paper is about

Abstract A simple route for synthesis of new tetrathiafulvalene dimethyl ester (TTF‐DME) is reported. The tetrathifulvalene dimethylester (TTF‐DME) has been prepared by introducing an ester coordination function as a bifunctional new donor. The redox behavior of the TTF‐DME was investigated in comparison to the well‐known dibenzotetrathiafulvene (DB‐TTF) by cyclic voltammetry. A two‐electron redox behavior was observed as a two waves.

Why it matters

OpenAlex reports 13 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract A simple route for synthesis of new tetrathiafulvalene dimethyl ester (TTF‐DME) is reported. The tetrathifulvalene dimethylester (TTF‐DME) has been prepared by introducing an ester coordination function as a bifunctional new donor. The redox behavior of the TTF‐DME was investigated in comparison to the well‐known dibenzotetrathiafulvene (DB‐TTF) by cyclic voltammetry. A two‐electron redox behavior was observed as a two waves.

Key concepts: Tetrathiafulvalene, Chemistry, Cyclic voltammetry, Redox, Bifunctional, Electrochemistry, Combinatorial chemistry, Inorganic chemistry

Related papers

Related paper 1Related paper 2
Back to paper searchBrowse research topicsOriginal source
Synthesis and electrochemical studies of tetrathiafulvalene derivatives (TTFs) as redox active ligands — Research Paper | ScholarLens