Issue 8, 1996

Crown-annelated tetrathiafulvalenes: synthesis of new functionalised derivatives and spectroscopic and electrochemical studies of metal complexation

Abstract

Synthetic routes to the first unsymmetrical annelated tetrathiafulvalene–S2O4 crowns are reported; the methodology is versatile, affording the parent system 8, functionalised derivatives 6, 7 and 9–12, and amphiphilic derivatives 6 and 13. UV–VIS spectroscopic studies of metal binding (Na+, Ag+ and Ba2+) to the crown–TTF systems 8 and 13, and the bis(crown)–TTF 14 have been performed in solution, and stability constants have been calculated. The data establish that for the crown compounds 8 and 13 1 : 1 complexes are formed, whereas for the bis(crown) compound 14 both 1 : 1 [14(Na+)] and 1 : 2 [14(Na+)2] complexes are formed. Solution electrochemical studies reveal that metal complexation to the crown unit leads to a small anodic shift in the first oxidation potential of the TTF system. Langmuir–Blodgett films of amphiphilic compound 13 have been assembled on solid substrates by Y-type deposition.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1996, 1587-1593

Crown-annelated tetrathiafulvalenes: synthesis of new functionalised derivatives and spectroscopic and electrochemical studies of metal complexation

R. Dieing, V. Morisson, A. J. Moore, L. M. Goldenberg, M. R. Bryce, J. Raoul, M. C. Petty, J. Garín, M. Savirón, I. K. Lednev, R. E. Hester and J. N. Moore, J. Chem. Soc., Perkin Trans. 2, 1996, 1587 DOI: 10.1039/P29960001587

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