1. Reactions of imidazol(in)-2-ylidenes with electron deficient fluoroolefins.
- Author
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Arduengo, Anthony J., Calabrese, Joseph C., Rasika Dias, H. V., Davidson, Fredric, Goerlich, Jens R., Jockisch, Alexander, Kline, Michael, Marshall, William J., and Runyon, Jason W.
- Subjects
IMIDAZOLES ,ELECTRON-deficient compounds ,FLUOROOLEFINS ,CYCLOBUTENE derivatives ,COMPLEX compounds ,NUCLEAR magnetic resonance spectroscopy ,X-ray crystallography - Abstract
1,3-Bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene forms stable 1:1 adducts with tetrafluoroethylene (2), hexafluorocyclobutene (3), and octafluorocyclopentene (4). Adduct2shows properties typical for nonpolarized olefins, as indicated by NMR spectroscopy and X-ray crystallography. By contrast, adducts3and4are best described as ylides with a significant charge separation between the imidazoline ring and the perfluorocycloalkyl unit. Similarly, 1,3-di-1-adamantylimidazol-2-ylidene reacts with tetrakis(trifluoromethyl)allene to form a polarized trimethylenemethane derivative, and bis(trifluoromethyl)ketene to form an imidazolium enolate zwitterion. The synthesis and characterization of a number of fluorinated methyleneimidazolines are described herein. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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