An investigation of the complexation behaviour of structurally modified tetrathiafulvalene derivatives with the electron deficient cyclophane cyclobis(paraquat-p-phenylene)

Bryce, M.R.; Cooke, G.; Duclairoir, F.M.A.; Rotello, V.M.

Abstract

This study has shown that easily oxidisable TTF units form charge-transfer (C-T) complexes with 7 which have the largest reported association constants to date. Replacing the sulfur of the TTF unit with selenium or extending the conjugated link between the two dithiole rings reduces the K-a of the complex relative to the parent derivative. (C) 2001 Published by Elsevier Science Ltd.

Citation

Bryce, M., Cooke, G., Duclairoir, F., & Rotello, V. (2001). An investigation of the complexation behaviour of structurally modified tetrathiafulvalene derivatives with the electron deficient cyclophane cyclobis(paraquat-p-phenylene). Tetrahedron Letters, 42(6), 1143-1145

• Journal Article Type: Article
• Publication Date: 2001-02
• Journal: Tetrahedron Letters
• Print ISSN: 0040-4039
• Publisher: Elsevier
• Peer Reviewed: Peer Reviewed
• Volume: 42
• Issue: 6
• Pages: 1143-1145
• Public URL: https://durham-repository.worktribe.com/output/1589178
• Publisher URL: <Go to ISI>://000166894400044