Trimethyltetrathiafulvalene bearing an N-methylpyridinium substituent: Synthesis, crystal structures, and charge transfer properties
Journal Article
Moore, A., Batsanov, A., Bryce, M., Howard, J., Khodorkovsky, V., Shapiro, L., & Shames, A. (online). Trimethyltetrathiafulvalene bearing an N-methylpyridinium substituent: Synthesis, crystal structures, and charge transfer properties. European Journal of Organic Chemistry, 73-78
The synthesis of 4,4',5-trimethyl-5'-(4-pyridyl)tetrathiafulva- lene (3), has been accomplished by reaction of the stannylated precursor 2 with 4-bromopyridine. Alkylation of 3 affords the N-methylpyridinium salt 4 which displays intramolecular charg... Read More about Trimethyltetrathiafulvalene bearing an N-methylpyridinium substituent: Synthesis, crystal structures, and charge transfer properties.