Formation of Attractive π-Redox Cyclophanes-Reference-Cited by-同舟云学术

Formation of Attractive π-Redox Cyclophanes

Published:1997-08-01 Issue:17 Volume:62 Page:6086-6089
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hascoat Philippe¹,Lorcy Dominique¹,Robert Albert¹,Carlier Roger¹,Tallec Andre¹,Boubekeur Kamal¹,Batail Patrick¹

Affiliation:

1. Laboratoire de synthèse et électrosynthèse organiques, UMR 6510, Université de Rennes, Campus de Beaulieu, 35042 Rennes, France, and Laboratoire de chimie des solides, Institut des Matériaux de Nantes, 2 rue de la Houssinière, 44072 Nantes, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo970322u

Reference21 articles.

1. Dimeric Tetrathiafulvalenes: New electron donors

2. Oligomeric Tetrathiafulvalenes: Extended donors for increasing the dimensionality of electrical conduction

3. Tetrathiafulvalenes as building-blocks in supramolecular chemistry

4. Synthesis of macrobicyclic tetrathiafulvalenophanes with three TTF bridges

5. Electrochemical Synthesis of Extended TTF

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