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Updated: Apr 8, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring
Sébastien Bivaud1, Sébastien Goeb1, Vincent Croué1
1Laboratoire MOLTECH-Anjou, Université d'Angers, UMR CNRS 6200, 2 bd Lavoisier, 49045 Angers Cedex, France. , Tel: 0033241735405.
Abstract:
The synthesis of a new Pd coordination-driven self-assembled ring M6L3 constructed from a concave tetrapyridyl π-extended tetrathiafulvalene ligand (exTTF) is described. The same ligand is also able to self-assemble in a M4L2 mode as previously described. Herein, we demonstrate that the bulkiness of the ancillary groups in the Pd complex allows for modulating the size and the shape of the resulting discrete self-assembly, which therefore incorporate two (M4L2) or three (M6L3) electroactive exTTF sidewalls.
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