Extreme Conformational Constraints in π-Extended Tetrathiafulvalenes: Unusual Topologies and Redox Behavior of Doubly and Triply Bridged Cyclophanes
Author:
Affiliation:
1. Contribution from the Department of Chemistry, University of Durham, Durham DH1 3LE, U.K.
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja062358m
Reference62 articles.
1. Salts of extended tetrathiafulvalene analogues: relationships between molecular structure, electrochemical properties and solid state organisation
2. (a) Martín, N.; Ortí, E. InHandbook of Advanced Electronic PhotonicMaterials and Devices; Nalwa, H. S., Ed., Academic Press: San Diego, 2001; Vol. 3, Chapter 6, pp 245−265.
3. Tetrathiafulvalenes, Oligoacenenes, and Their Buckminsterfullerene Derivatives: The Brick and Mortar of Organic Electronics
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