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Synthesis of tetrahydroxy-π-extended tetrathiafulvalenes as new supramolecular redox building blocks

✍ Scribed by Marta C Dı́az; Beatriz Illescas; Nazario Martı́n


Book ID
104252849
Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
180 KB
Volume
44
Category
Article
ISSN
0040-4039

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✦ Synopsis


A novel p-quinonoid p-extended tetrathiafulvalene (exTTF) endowed with four hydroxy groups with different reactivity (phenol and alcohol) has been synthesized as a supramolecular redox building block. The redox properties, studied by cyclic voltammetry, reveal a strong donor ability and, despite the different substitution pattern on the 1,3-dithiole rings, only one oxidation wave involving two electrons to form the dication species.


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