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Cover Picture: The First Studies of a Tetrathiafulvalene-σ-Acceptor Molecular Rectifier (Chem. Eur. J. 10/2005)

✍ Scribed by Gregory Ho; James R. Heath; Mykola Kondratenko; Dmitrii F. Perepichka; Karin Arseneault; Michel Pézolet; Martin R. Bryce


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
328 KB
Volume
11
Category
Article
ISSN
0947-6539

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✦ Synopsis


The role of diads…︁ in molecular electronics has been investigated with the recently synthesized tetrathiafulvalene‐σ‐trinitrofluorene diad (depicted on the cover). As determined by cyclic voltammetry, the HOMO–LUMO gap of this diad is as low as ∼0.3 eV, close to that of the theoretical Aviram–Ratner TTF‐σ‐TCNQ molecular rectifier. The rectification behavior of this molecule was tested as a function of electrode material (Si/Ti and Au/Hg), alignment, and orientation of the molecules in the junction. For more information, see the paper by J. R. Heath, D. F. Perepichka et al. on page 2914 ff.


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The First Studies of a Tetrathiafulvalen
✍ Gregory Ho; James R. Heath; Mykola Kondratenko; Dmitrii F. Perepichka; Karin Ars 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 426 KB

## Abstract Langmuir–Blodgett monolayers of a donor–acceptor diad TTF‐σ‐(trinitrofluorene) (**8**) with an extremely low HOMO–LUMO gap (0.3 eV) have been used to create molecular junction devices that show rectification behavior. By virtue of structural similarities and position of molecular orbita